Aldehydes

3,4-Dihydroxy-6-nitrobenzaldehyde is a nitrite that can be used to produce nitric acid. It can also be used in the synthesis of caffeic acid and protocatechuic aldehyde. This molecule is also a catalyst for the conversion of 3,4-dihydroxybenzoic acid to chloride and purine derivatives. 3,4-Dihydroxy-6-nitrobenzaldehyde is nucleophilic and can react with an electron pair donor such as methyl ester or dimerization. The product of this reaction is an unsaturated compound called hyperuricemic mice.

<p>4-Iodobenzaldehyde is a chemical compound with the molecular formula C6H5IO. It is an aromatic compound that can be used in cancer therapy. 4-Iodobenzaldehyde reacts with trifluoroacetic acid to form an intramolecular hydrogen, which is detected using a low-energy monomer and high detection sensitivity. 4-Iodobenzaldehyde has two phenyl substituents and a serine protease functional group, which are required for its interaction with other molecules. The presence of these functional groups allows analytical methods to be used to identify 4-iodobenzaldehyde in various samples. Using analytical methods, it can be determined that 4-iodobenzaldehyde interacts with an acceptor molecule at the reaction vessel thermally or by irradiation.</p>

<p>2,2,7-Trimethyl-2,3-dihydro-1-benzofuran-5-carbaldehyde is a fine chemical that is used as a building block in research and synthesis of other chemicals. It has been shown to be a versatile building block for the synthesis of complex compounds. 2,2,7-Trimethyl-2,3-dihydro-1-benzofuran-5-carbaldehyde is also a useful intermediate to make other chemicals as well as a reagent in the production of speciality chemicals. This compound can be used in reactions with amines and alcohols. It has been found to have high quality that makes it useful for use in reactions with DNA and RNA nucleotides and proteins.</p>

<p>4-Chlorobenzaldehyde oxime is an antibacterial agent that is classified as a chloroamine. It has been shown to be an effective inhibitor of bacterial growth, with a low toxicity to mammalian cells. 4-Chlorobenzaldehyde oxime has been shown to be activated by amines and hydroxylamine, and the resulting intermediate can cleave a variety of bonds in the bacterial cell wall. The molecular orbitals of this compound have been calculated using crystallographic data and functional theory. 4-Chlorobenzaldehyde oxime also binds to chloride ions and forms a complex with ammonium nitrate, which may account for its activity against some bacteria that are resistant to chlorinated compounds (e.g., Clostridium difficile). This compound also contains functional groups that may react with disulfides present in the bacterial cell wall.</p>

<p>4-(Phenylethynyl)benzaldehyde is a synthetic compound that belongs to the class of aldehydes. It is soluble in acetonitrile and can be synthesized by a cross-coupling reaction between two different organometallic reagents, such as N-phenyltrifluoroacetamide or N-phenylmaleimide. 4-(Phenylethynyl)benzaldehyde has been shown to have cytotoxic effects on cancer cells and can be used for the treatment of leukemia and Hodgkin's lymphoma. This chemical has fluorescence properties, which are enhanced by surface-enhanced Raman spectroscopy. 4-(Phenylethynyl)benzaldehyde also shows photophysical properties, such as an imine and fluorescent character, making it possible to use it in chemiluminescence reactions.</p>

<p>4-Fluoro-3-hydroxybenzaldehyde is a fluorescent chemical that belongs to the group of alcohols. It has been shown to have the following properties: an excitation wavelength of 285 nm, a fluorescence wavelength of 350 nm, and a quantum yield of 0.004%. The solvent effect on 4-fluoro-3-hydroxybenzaldehyde's fluorescence intensity is approximately linear with concentration, but the fluorescence profile is dependent on the polarity of the solvent. The phenyl group of 4-fluoro-3-hydroxybenzaldehyde causes it to be more polarizable than other molecules in its class. The kinetic rate constants for 4-fluoro-3-hydoxybenzaldehyde were found by measuring the decay rates of its fluorescence emission as a function of time.</p>

<p>6-Bromoveratraldehyde (6BrA) is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and has been used as a model study for biphenyl and naphthalene. 6BrA induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell.</p>

<p>4-Fluoro-1H-indole-3-carbaldehyde is a chemical compound that can be used as a reagent, reaction component, or building block in the synthesis of more complex compounds. This chemical is also known as CAS No. 23073-31-6 and has high quality and purity. 4-Fluoro-1H-indole-3-carbaldehyde is useful for research purposes and can be used as a speciality chemical or a fine chemical.</p>

<p>2-Aminobenzaldehyde is an aromatic compound that contains a hydroxyl group, two nitrogen atoms, and an anhydrous sodium. It can be synthesized by the reaction of hydroxybenzaldehyde with trifluoroacetic acid or nitrobenzene. 2-Aminobenzaldehyde is used as a precursor to other compounds, such as 2-aminobenzonitrile and 2-aminophenol. It also reacts with anthranilic acid in the presence of sodium salts to give a variety of pyrazoles. This product has been shown to react with epidermal growth factor (EGF) in the presence of light to produce light emissions.</p>

<p>5-Fluoro-2-methylbenzaldehyde is a fine chemical that is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic molecules. It is also useful in the preparation of synthetic resins, dyes, and flavors. 5-Fluoro-2-methylbenzaldehyde has been shown to be a versatile building block with many potential applications. This molecule can be used as a reaction component or as a speciality chemical to produce high quality reagents.</p>

<p>2,3,4-Trimethoxy-6-methylbenzaldehyde is a synthetic coumarin with antibacterial activity. It is synthesized by the condensation of 3-hydroxyacetophenone and benzaldehyde. 2,3,4-Trimethoxy-6-methylbenzaldehyde has been shown to have antibacterial activity against both Gram-positive and Gram-negative bacteria. This molecule has also been shown to inhibit the growth of Gram negative bacteria in the presence of hydrogen peroxide. The crystal structure of this molecule was determined by XRD analysis and shows that it contains a dihedral angle of about 155°.</p>

<p>2-Methylveratraldehyde is a chiral compound that can be used as a reagent in organic synthesis. It has been shown to be a potentiator of the antimicrobial activity of grignard reagents and carbonation, which are chemical reactions that form new carbon-carbon bonds. 2-Methylveratraldehyde also has biological studies, such as its use as an inducer of phytoalexin production in plants.</p>

<p>Please enquire for more information about 2-(2-Chlorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Hydroxy-3-methoxybenzaldehyde is a model compound that is used to study the reaction mechanism of hydrogen bonding. It has been shown to have antioxidative properties and amoebicidal activity. The biological properties of 2-hydroxy-3-methoxybenzaldehyde are still being studied. There are also no reports on its toxicity or carcinogenicity in humans. This compound is a member of the group P2, which includes compounds with two aromatic rings connected by one carbon atom. The molecular geometry around this carbon atom is pyramidal and the molecule can exist in either an axial or equatorial orientation. Synchronous fluorescence experiments have shown that 2-hydroxymethoxybenzaldehyde reacts with Toll-like receptor 4 (TLR4).</p>

<p>4-(Trifluoromethylthio)benzaldehyde is a magnetic, stereogenic, mononuclear compound with a thermodynamic stability that has been improved by advances in the field of thermodynamics. The compound can also be synthesized using an asymmetric synthesis and is tetrasubstituted with antiferromagnetic coupling. 4-(Trifluoromethylthio)benzaldehyde has many functions, including being able to control the oxidation-reduction potentials of lanthanide ions and ferromagnetic materials. It also has a calorimetry effect on the adsorption of water vapor onto hydrophobic surfaces.</p>

<p>3-Methoxy-4-methylbenzaldehyde is a chemical compound that belongs to the class of phenylpropanoids. It has been shown to have a variety of uses, including as a drug substance and in natural products. 3-Methoxy-4-methylbenzaldehyde can be used for labeling, mass spectrometric detection, physicochemical techniques, and chromatographic science. The compound can be detected using electron ionization, mass spectrometric detection, or chromatographic science. Isomers of this compound are often difficult to identify due to the presence of other similar compounds.</p>

o-Nitrocinnamaldehyde is an aldehyde that belongs to the group of β-unsaturated aldehydes. It has been shown to inhibit cancer cell growth in vitro and in vivo. o-Nitrocinnamaldehyde inhibits xanthine oxidase by preventing the oxidation of hypoxanthine to xanthine and xanthine to uric acid. This prevents the formation of superoxide radicals, which are known carcinogens. The compound also inhibits aldehyde dehydrogenase, which prevents the oxidation of nitro compounds that have been generated by nitrosation reactions. These reactions are catalyzed by nitric oxide synthases (NOS) and convert nitrate into nitrite and then into reactive nitrogen species such as peroxynitrites. o-Nitrocinnamaldehyde also inhibits uv absorption, which may be due to its ability to form supramolecular aggregates with other organic molecules or metal ions.

<p>2-(4-Chlorophenyl)-4,4-dimethyl-1-cyclohexene-1-carboxaldehyde is a high quality reagent that can be used as a useful intermediate in the production of complex compounds. It is also a fine chemical with CAS No. 1228837-05-5 and is useful scaffold for the production of speciality chemicals. This compound has been identified as a useful building block with versatile uses in research and development, such as reaction components in organic synthesis.</p>

<p>4-Hydroxybenzaldehyde is a phenolic compound that is produced in plants. 4-Hydoxybenzaldehyde is used as an extractant for sodium carbonate and hydroxyl group from acetate extract. The locomotor activity of animals was tested following administration of this substance, and it has been shown to have a high resistance against x-ray crystallography. The reaction mechanism for the formation of p-hydroxybenzoic acid from 4-hydroxybenzaldehyde has been proposed, which may be due to the oxidation of 4-hydroxybenzaldehyde by hydrogen peroxide. This reaction also induces apoptosis pathway in cells. Kinetic data for the reaction between 4-hydroxybenzaldehyde and hydrogen peroxide were obtained using UV spectroscopy.</p>

<p>2-Chloro-6-fluorobenzaldehyde oxime is the chemical compound with the formula ClCH=C(O)N(OH)Cl. It is a white solid that is soluble in water and ethanol. 2-Chloro-6-fluorobenzaldehyde oxime is used as a versatile building block in organic synthesis, for example as a reagent for the preparation of amides, esters, and nitriles. It is also useful as a reagent for the conversion of ketones to nitriles.</p>

<p>Terephthaldicarboxaldehyde is a white crystalline solid that has been shown to be soluble in hydrogen fluoride, water vapor, and sodium salts. It is also insoluble in water. Langmuir adsorption isotherm experiments have shown that the solubility of terephthaldicarboxaldehyde increases with increasing concentration of chitosan polymer. Terephthaldicarboxaldehyde has been used as an analytical method for p-hydroxybenzoic acid (PHBA) and terephthalic acid (TPA). It can also be used as a fluorescent probe to detect the presence of these compounds in aqueous solutions.</p>

<p>4-Acetamidobenzaldehyde is an organic compound that has been shown to exhibit inhibitory effects on influenza virus replication in cell culture. 4-Acetamidobenzaldehyde is a dihedral molecule with a p2 group and can be synthesized from benzaldehyde and acetamide. It has also been shown to have potential use in the treatment of tuberculosis. The biological properties of 4-acetamidobenzaldehyde are not well understood, but it is thought that uptake may occur through the imine nitrogen. This molecule has been detected in tissue samples such as lung, liver, and kidney.</p>

<p>3,5-Dichlorobenzaldehyde is an organic compound with the formula CHClO. It is a colorless liquid that smells like freshly cut grass. 3,5-Dichlorobenzaldehyde is used in organic synthesis as an electrophile for the preparation of substituted benzoquinones and other heterocycles. It is also used to prepare aromatic amines via aldol condensation with ketones. In addition, it can be used to generate azides from nitroarenes or nitroalkanes in the presence of sodium azide or potassium azide. Finally, it can be used to synthesize molybdenum compounds such as molybdic acid and ammonium molybdate.</p>

<p>Please enquire for more information about 2-Hydroxy-4-morpholinobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-(4-Chlorophenyl)-2-furaldehyde (5-CPFA) is an antitubercular drug that inhibits the growth of tuberculosis bacteria by disrupting the synthesis of DNA. It is a functional theory that 5-CPFA inhibits the bacterial enzyme, chalcone hydroxylase, which is involved in the conversion of chalcones to flavones. This inhibition prevents the formation of reactive oxygen species and leads to cell death. The mechanism of action for 5-CPFA has been shown to be due to its ability to form covalent bonds with metal ions such as copper, zinc, and iron. When exposed to ultraviolet radiation, this compound reacts with these metal ions and causes bond cleavage in DNA strands. The resulting damage in DNA strands leads to cell death within hours.</p>

<p>3-Fluoropyridine-4-carboxaldehyde is a reactivator that can be used in the treatment of bladder cancer. It binds to pyridinium and oxime derivatives, which are present in proteins, to form a reactive intermediate. This intermediate reacts with aldehyde groups on hemoglobin, restoring the oxygen binding capacity of hemoglobin to levels seen in healthy individuals. 3-Fluoropyridine-4-carboxaldehyde has been shown to have anticancer activity against bladder cancer cells and also has potential use as an additive for the treatment of red blood cells.</p>

<p>3-Bromo-5-chloro-2-hydroxybenzaldehyde is a molecule that contains nitrogen atoms. It has coordination geometry and a chelate ring. 3-Bromo-5-chloro-2-hydroxybenzaldehyde also has electrochemical properties, which can be studied by cyclic voltammetry. This molecule is a copper complex that exhibits fluorescence properties and dihedral angles. The magnetic resonance spectrum of 3-bromo-5-chloro-2 hydroxybenzaldehyde displays hydrogen bonding interactions and an imine nitrogen. 3BChBrOH also absorbs light at wavelengths of 280 nm (max) and 240 nm (min).</p>

<p>1-Naphthaldehyde is a coordination compound that contains 1 naphthyl group and an oxygen atom. It can be used as an oxidation catalyst, intramolecular hydrogen, or a reaction solution. The antimicrobial activity of 1-naphthaldehyde has been shown in the presence of sodium carbonate or potassium phosphate buffer. 1-Naphthaldehyde has been shown to possess structural properties similar to those of other metal chelates, such as zinc pyrithione. The protonated form of 1-naphthaldehyde has been identified by means of analytical methods including gas chromatography and mass spectrometry.</p>

<p>4-Hydroxy-3-nitrobenzaldehyde (4NBA) is a chemical compound that belongs to the class of aromatic compounds. It is an intermediate in the synthesis of various pharmaceuticals, including benzocaine and nitroglycerin, and has been researched for its potential use in cancer diagnosis. 4NBA has shown optical properties that allow it to be used as a model system for studying the interactions between water and benzyl groups. It also possesses anti-inflammatory properties due to its ability to inhibit the production of inflammatory cytokines such as IL-1β, IL-6, and TNFα.</p>

<p>2-fluoro-4-(trifluoromethyl)benzaldehyde is a chemical compound that can be synthesized by the reaction of peroxide with fluorine. It is used as a solvent in coatings and in the production of organic chemicals. 2-fluoro-4-(trifluoromethyl)benzaldehyde has been shown to be toxic to cancer cells at high concentrations, but not normal cells. The waveguide effect can be observed at temperatures below -60°C and it has three functional groups that are hydrolyzed by HCl.</p>

<p>3-Benzyloxybenzaldehyde (3BOBA) is a hydrochloride salt of 3-benzyloxybenzaldehyde. 3BOBA has shown anti-inflammatory activity in hl-60 cells and prostate cancer cells through inhibition of the activation of nuclear factor kappa B. This inhibition was found to be due to the apoptosis protein, survivin, which was downregulated by 3BOBA treatment. The analogs of 3BOBA are known as curcumin analogs, and have shown anticancer properties in clinical trials.</p>

<p>3,4-Dihydroxy-5-methoxybenzaldehyde is a synthetic compound that has shown to have inhibitory effects on the replication of DNA and RNA. It also inhibits the growth of bacteria in culture by binding to the nucleic acid. The chemical structure of 3,4-Dihydroxy-5-methoxybenzaldehyde is similar to that of bisbenzylisoquinoline alkaloids, which are found in plants such as opium poppy. This similarity may explain its ability to inhibit bacterial growth. 3,4-Dihydroxy-5-methoxybenzaldehyde may be used as a drug candidate for treating bacterial infections.</p>

<p>3,4-Dichlorobenzaldehyde oxime is a natural carotenoid that has been shown to have antibacterial activity. 3,4-Dichlorobenzaldehyde oxime is produced by the reaction of malonate and aldehyde in an incubated system. This compound has been shown to be active against Gram-positive bacteria such as staphylococcus and aldoximes and Gram-negative bacteria such as E. coli, Salmonella typhimurium, and Shigella flexneri. 3,4-Dichlorobenzaldehyde oxime inhibits bacterial growth by binding to the 50S ribosomal subunit of the bacterial cell membrane. This binding prevents protein synthesis, leading to cell death. The biosynthesis of 3,4-dichlorobenzaldehyde oxime involves the conversion of abscisic acid (ABA) into ABA quinone through oxidation by an enzyme called ABA oxidase</p>

<p>4-n-Propylbenzaldehyde is a chemical compound that belongs to the group of aromatic aldehydes. It is used in the production of other chemicals, such as pharmaceuticals and fragrances. 4-n-Propylbenzaldehyde has been shown to be genotoxic, causing DNA damage and mutating genes. This chemical also has an inhibitory effect on cancer cells, which may be due to its ability to interfere with histone deacetylase activity. The genotoxic potential of this substance is considered low based on its lack of genotoxicity in vitro and in vivo. This compound does not have any structural formula for the corresponding metal complex.</p>

<p>Please enquire for more information about 2-(4-Fluorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Fluoro-2-methoxybenzaldehyde is a synthetic chemical that has been used as a precursor in the synthesis of pharmaceuticals and other organic compounds. 3-Fluoro-2-methoxybenzaldehyde can be prepared through the lithiation, chloromethylation, or trimethylation of 3-fluoroacetophenone. The compound can be oxidized to 3,4-dihydrobenzofuran with peroxide at low temperature. This conversion can be achieved using a variety of reagents, such as boron tribromide or boron trichloride.</p>

<p>4-Diethylamino-2-methoxybenzaldehyde (4DMMB) is a protonated molecule that is able to penetrate the mitochondrial membrane due to its low charge. Once inside, 4DMMB can be reduced by electron transfer from the mitochondria's membrane potential. This reduction leads to an increase in the mitochondrial membrane potential and subsequent photophysical emissions. The introduction of 4DMMB has been shown to cause mitochondrial membrane potential changes in cells, which may lead to pathophysiologic conditions such as cancer.</p>

<p>3-Nitro-4-chlorobenzaldehyde is a copper complex that has been used in the study of molecular interactions. The molecule has been studied by a number of techniques, including binding experiments, vibrational spectroscopy, and light emission. 3-Nitro-4-chlorobenzaldehyde has shown bacteriostatic activity against Escherichia coli and Bacillus subtilis. This compound also appears to have potential as a drug target due to its ability to inhibit the growth of Pseudomonas aeruginosa. 3-Nitro-4-chlorobenzaldehyde may be useful in the treatment of industrial processes involving nitric acid.</p>

<p>Triphenylphosphoranylidene)acetaldehyde (TPPAA) is a diphenyl ether that binds to the allosteric site on the enzyme acetylcholinesterase, leading to inhibition of the catalytic mechanism. TPPAA has been shown to have insecticidal activity in the form of contact toxicity. It also has anticancer activity by inhibiting DNA synthesis and inducing apoptosis in cancer cells. TPPAA can be synthesized through a preparative method involving an asymmetric synthesis with a hydroxyl group as one of the reagents. TPPAA is an ionizable molecule that undergoes chemical ionization in a mass spectrometer and vibrational spectroscopy techniques.</p>

<p>3,4-Dihydroxybenzaldehyde is an active compound that is a protocatechuic aldehyde. It has been shown to inhibit protein oxidation and kidney injury. 3,4-Dihydroxybenzaldehyde also inhibits the production of bcl-2 protein and growth factor-β in rat urine. This compound has been used in Chinese medicinal preparations as well as in control methods for oxidizing agents.</p>

<p>2,4,5-Trimethoxybenzaldehyde is a natural compound that belongs to the group of sephadex g-100. It is used as an absorbent and has been shown to react with human immunoglobulin in the presence of tiglic acid. The reaction mechanism for this chemical is not well understood but it is believed that intermolecular hydrogen bonding may be occurring. 2,4,5-Trimethoxybenzaldehyde has been shown to have anti-inflammatory effects when tested on rats in a laboratory setting. This chemical has also been used as an analytical reagent for biological samples and biological studies as well as a preparative hplc column. Optical sensors have also been used to detect this chemical in various types of optical sensing experiments. X-ray crystal structures have also been obtained for this compound using synchrotron radiation.</p>

<p>2-Nitro-4,5-methylenedioxybenzaldehyde (2NMB) is a molecule with a molecular weight of 188.24, an empirical formula of C8H8NO2 and a chemical structure consisting of a benzene ring attached to two nitro groups. 2NMB has been shown to bind to the dopamine β-hydroxylase enzyme in human serum and inhibit the production of dopa, which leads to a decrease in dopamine levels. It also inhibits the growth of staphylococcus, cryptococcus neoformans, and typhimurium. 2NMB also has been used as radiotracers for gyrase activity and can be used for asymmetric synthesis due to its piperonal group. The uptake of 2NMB by cells is dependent on its nucleophilic properties.</p>

<p>2-Bromo-4-cyanobenzaldehyde is a potent protease inhibitor and can be used as an antiviral agent. It inhibits the NS3 protease of hepatitis C virus (HCV) with IC50 of 0.2 μM. 2-Bromo-4-cyanobenzaldehyde has been evaluated for its ability to inhibit replicons from HCV genotypes 1, 2, 3, 4 and 5 with varying degrees of potency. In vitro studies have shown that 2-bromo-4-cyanobenzaldehyde is a potent inhibitor of HCV NS3 protease, demonstrating activity against all major HCV genotypes in cell culture. This molecule has also been shown to inhibit the replication of HIV, herpes simplex virus type 1 and human rhinovirus type 2 in cell culture.</p>

<p>4-Bromo-3,5-dimethylbenzaldehyde is an organic compound that contains a benzene ring with a bromine atom in the 4 position. It is used as a reagent and intermediate in organic synthesis. The compound can be converted to radical cations by reaction with electron-deficient alkylating agents such as methyl iodide or trimethylsilyl chloride. Radical cations are classified as reactive intermediates and have been shown to react with other organic compounds to form new products.</p>

<p>4'-(3,4-Difluorophenoxy)benzaldehyde is an organic compound that yields a bright yellow color. It is used in the replication of DNA and RNA in the laboratory. This compound has been shown to interact with environmental conditions and significant effects have been observed for cultivars of wheat.</p>

<p>4-Fluorobenzaldehyde is an organic compound that is used in the synthesis of other chemicals. 4-Fluorobenzaldehyde has been shown to have hemolytic activity and to be a copper complex that reacts with hydrochloric acid. The reaction mechanism of 4-fluorobenzaldehyde with copper chloride is thought to involve the formation of a copper complex, which then undergoes nucleophilic attack by the trifluoroacetic acid, forming a positronium ion. This positronium ion then reacts with hydroxide ions from water, forming hydrogen peroxide and a pyrimidine compound.</p>

<p>beta-Resorcylic aldehyde oxime is a compound that can be used as a reagent, speciality chemical, and research chemical. It has the CAS number 5399-68-8, and it is a fine chemical that has been shown to be useful in organic synthesis. beta-Resorcylic aldehyde oxime is soluble in methanol, ethanol, benzene, diethyl ether, and acetone. This compound can be used as a building block for other compounds by reacting with amines or carboxylic acids. It can also be used as an intermediate for other reactions. beta-Resorcylic aldehyde oxime has been shown to have versatile properties that make it an excellent scaffold for creating new compounds.</p>

<p>3,4,5-Trihydroxybenzaldehyde monohydrate is a chemical compound that belongs to the class of aromatic hydrocarbons. It has been shown to have a neurotoxic effect on the mouse brain and is used in the diagnosis of neurological diseases. 3,4,5-Trihydroxybenzaldehyde monohydrate is also used as an intermediate in the synthesis of other chemicals. The molecular formula for this substance is C9H7O3 and it contains three nitrogen atoms. The molecular weight is 179.06 g/mol and its sequence length is 707 amino acids long. This substance has been found to be present in humans with chronic kidney disease and insulin resistance.</p>

<p>5-Hydroxy-3-methyl-1H-pyrazole-4-carbaldehyde is an organic compound that is used as a building block in the synthesis of a variety of complex compounds. It can be used as a reaction component and is also useful in the production of speciality chemicals. 5-Hydroxy-3-methyl-1H-pyrazole-4-carbaldehyde has been shown to form complexes with metals, such as copper, silver, and gold. These complexes are useful for research into catalytic reactions and electrochemistry. This chemical is also used in the production of pharmaceuticals, agrochemicals, and other high quality reagents.</p>

<p>4-Ethoxybenzaldehyde is a chemical compound with antioxidant properties. It has been found to inhibit the proliferation of cervical cancer cells and melanoma cells, as well as to protect against radiation-induced oxidative damage in human skin. 4-Ethoxybenzaldehyde also inhibits the influenza virus by interfering with its ability to replicate. This compound is used in many different products, including cosmetics and pharmaceuticals. The most common use of 4-ethoxybenzaldehyde is as an excipient in tablet formulations. In this application, it can be used to maintain drug stability and improve disintegration time. In addition, it may have some anti-inflammatory effects that are related to its ability to inhibit the production of prostaglandins and leukotrienes. 4-Ethoxybenzaldehyde has been shown to have antioxidant properties for diabetics as well as for patients with autoimmune diseases such as multiple sclerosis and systemic lupus erythematosus (SLE). The</p>

<p>4-(Hydroxymethyl)benzaldehyde is a molecule that can be used as an immunosuppressant. The molecule has been shown to inhibit the activity of tyrosinase, which is an enzyme that catalyzes the oxidation of L-tyrosine to produce melanin. 4-(Hydroxymethyl)benzaldehyde has also been shown to have chemosensory properties, which may allow it to be used in chemical sensors. It has not yet been determined if this molecule is able to inhibit the production of melanin in humans or other mammals.</p>

<p>4-Hydroxy-2-methylbenzaldehyde is an organic compound that is a colourless to yellow liquid with a characteristic odor. It has antibacterial activity and can be used as a natural product. The yield of this compound from staphylococcus is about 50%. When 4-hydroxy-2-methylbenzaldehyde reacts with chalcone, it forms the hydroxychalcones. This process can be used to identify the presence of 4-hydoxy-2-methylbenzaldehyde in many different organisms. The phenolic ring in this compound can undergo formylation, which means it can be oxidized to form formic acid. This process also occurs in soil bacteria and may account for some of its antibacterial properties.</p>

<p>2,6-Dimethylbenzaldehyde oxime is a reagent and useful intermediate for the synthesis of complex compounds. It is also a building block for speciality chemicals. 2,6-Dimethylbenzaldehyde oxime has been used in research and as a reaction component for various organic syntheses. This compound has a CAS number of 55882-62-7.</p>

<p>Polydialdehyde starch is a cross-linking agent that is used to form hydrophobic polymers, which are prodrugs. It is a polymer of dialdehydes and can be used as an additive for restenosis prevention. Polydialdehyde starch has been shown to reduce platelet adhesion and aggregation in vitro and in vivo. The mechanism of action may be related to the ability of polydialdehyde starch to bind collagen and promote its degradation by hydrolysis. This also results in an increase in the rate of dilation of blood vessels, which may contribute to the antiplatelet effect. Polydialdehyde starch has been shown to be biodegradable, with a half-life of about two weeks in vivo after injection into rats.</p>

<p>3-Cyanopropionaldehydedimethylacetal (3CPDMA) is a reactive compound that inhibits the proliferation of muscle cells. It has been shown to inhibit the synthesis of 3-hydroxy-3-methylglutaryl coenzyme A, which is required for the production of cholesterol and fatty acids. This inhibition leads to a decrease in the growth of cells and their ability to divide. 3CPDMA has also been shown to have an inhibitory effect on picolinic acid, which is involved in the activation of receptors that induce cellular proliferation. The inhibition of this receptor may be due to its ability to compete with other ligands for binding sites on the receptor.<br>It has been shown that 3CPDMA acts as an antagonist against acarids, which are mites that feed on skin cells. This property may be due to its antagonistic effects on amino acid composition, which may affect calcium uptake by cells or cell membrane permeability.</p>

<p>2,5-Dimethoxy-4-methylbenzaldehyde is a bioactive chemical that has been shown to have anticancer activity. It has been shown to be an effective inhibitor of cancer cell growth in vitro and in vivo. 2,5-Dimethoxy-4-methylbenzaldehyde has also been shown to inhibit the formation of fatty acids and improve the uptake of glucose by cancer cells. This compound is a metabolite of the amino acid methionine and is used as a marker for mesenchymal cells. The structure of 2,5-dimethoxy-4-methylbenzaldehyde consists of two methoxy groups connected with an aliphatic chain consisting of one or more carbon atoms. This functional group may provide the anticancer activity through radical scavenging activities.</p>

<p>5-[(4,5-Dimethyl-4H-1,2,4-triazol-3-yl)thio]-2-furaldehyde is a versatile building block that can be used as a research chemical or reagent. It is also useful for the synthesis of complex compounds. This material has been shown to be an excellent starting point for the synthesis of high quality and useful scaffolds.</p>

<p>4-Bromo-3-methylbenzaldehyde is a versatile building block that is used in the synthesis of many complex compounds. It can be used as a reactant, reagent, or speciality chemical. 4-Bromo-3-methylbenzaldehyde is an intermediate for the production of other chemicals and has been shown to be useful in the synthesis of various scaffolds. This product has been shown to have high purity and quality.</p>

<p>6-Fluoroindole-3-carboxaldehyde (6FLA) is a synthetic compound that inhibits biosynthesis of the phytoalexins salicylic acid and lignin in plants. It also inhibits the β-glucuronidase enzyme, which hydrolyzes the glucuronide conjugates of phenolic compounds and xenobiotics. 6FLA has been shown to cause mild liver damage in rats, but its effects on humans are unknown. 6FLA may be used as a detectable substance for assays.</p>

<p>4-(Bromomethyl)benzaldehyde is a chemical compound that can be synthesized by the reaction of benzaldehyde with bromine in the presence of a base. This compound has been shown to bind to human immunoglobulin G, formyl group and photophysical properties. 4-(Bromomethyl)benzaldehyde has also been used as a model for cancer studies because it binds to DNA and forms an imine bond with thymine. It has been used as a reagent for analytical methods such as phosphotungstic acid, which is a reagent used to detect proteins. The mechanism of this compound is not yet fully understood, but it may involve the formation of an imine bond with thymine in DNA.</p>

<p>2-Chlorobenzaldehyde oxime is a compound that inhibits the growth of mycobacterium tuberculosis. It reacts with chloride in the environment to form 2-chlorobenzaldehyde, which reacts with an isoxazole to produce a quinone. Quinones are toxic to mammals and are thought to be responsible for the antimycobacterial activity of this compound. The reaction mechanism of 2-chlorobenzaldehyde oxime has been studied using various techniques and its toxicity has been evaluated in both culture and animal studies. This compound has shown no significant effects on mice at up to 100 mg/kg body weight, but it was found to cause death in rats at doses as low as 0.1 mg/kg body weight.<br>2-Chlorobenzaldehyde oxime was synthesised by reacting 2-chlorobenzaldehyde with oxalyl chloride under conditions suitable for safety, and the product was purified by recrystallisation from acetone. The synthesis</p>

<p>3-Ethoxy-4-methoxybenzaldehyde is a metabolite of the benzoquinone and 3-hydroxypropanoic acid pathway. It is an electron donor that serves as a substrate for fatty acid synthesis. This compound has been shown to have antiviral properties, as it inhibits the replication of influenza virus in vitro by interfering with viral RNA polymerase. It may also act as a regulatory molecule for uptake, although its precise role in this process is not yet known. 3-Ethoxy-4-methoxybenzaldehyde has been shown to be an optimal reactant with signal sequences from proteins, including biochemical pathways such as glycolysis and pentose phosphate shunt.</p>

<p>6-Benzyloxyindole-3-carboxaldehyde is a benzyl compound that is produced by the catalytic hydrogenolysis of benzyl alcohol. The debenzylation product of 6-benzyloxyindole-3-carboxaldehyde is known as benzene.</p>

<p>Please enquire for more information about 3,4-Dihydroxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,10-Phenanthroline-2-carbaldehyde is a phenylhydrazone compound that has been shown to have anticancer activity. It is also a supramolecular complex, which means it can form hydrogen bonds and coordinate bonds with other molecules. The anticancer activity of 1,10-phenanthroline-2-carbaldehyde may be due to its ability to inhibit the growth of prostate carcinoma cells. This compound also inhibits the growth of human cervical carcinoma cells by binding to their DNA and inhibiting the synthesis of RNA and protein. 1,10-Phenanthroline-2-carbaldehyde is being studied for its potential as an inhibitor of tumor angiogenesis.<br>1,10-Phenanthroline-2-carbaldehyde has been shown to have antiplatelet aggregation effects in platelets from healthy humans as well as those with type 2 diabetes mellitus or chronic kidney disease.</p>

<p>4-Phenoxybenzaldehyde is a phenolic compound that has potent inhibitory activity against bacteria. It was shown to have the highest antibacterial activity among alkanoic acids, with an MIC of less than 2 µg/mL. 4-Phenoxybenzaldehyde is produced by the condensation of phenol and acetaldehyde in the presence of a solid catalyst and potassium hydroxide. This reaction produces a mixture of products, including 4-phenoxybenzaldehyde, which can be purified by recrystallization or column chromatography. The biosynthetic pathway for 4-phenoxybenzaldehyde in plants has been elucidated and includes two steps: one involving pyrazole ring formation and another involving hydroxyl group formation.</p>

<p>4-Bromo-2-hydroxybenzaldehyde is a chemical compound that is used in the synthesis of azides. It has a molecular formula of C6H5BrO, a diameter of 197.037 pm, and a structural formula of CHBrO. 4-Bromo-2-hydroxybenzaldehyde can be prepared by reacting bromine with hydroxybenzaldehyde in the presence of an amine catalyst. This product has been shown to have synergistic effects when used in combination with other anticancer agents such as aminopyrimidines, coumarin derivatives, or 2-(4'-hydroxyphenyl) benzoxazole. The photophysical properties of 4-bromo-2-hydroxybenzaldehyde are characterized by its fluorescence emission at 272 nm and its absorption at 270 nm. This product also shows low detection levels in human liver tissue samples, which may be due to its high water sol</p>

<p>3-Hydroxy-4-iodobenzaldehyde is a fluorophore that is used in the synthesis of amide compounds, as well as in the production of other synthetic molecules. 3-Hydroxy-4-iodobenzaldehyde has been shown to have pharmacokinetic properties that are similar to those of fluorescein, and can be used to study the distribution and metabolism of this compound. This compound also has an oxidation potential that is higher than that of fluorescein, which makes it more useful for studying drug metabolism. The labile nature of 3-hydroxy-4-iodobenzaldehyde means it will not remain intact for long periods of time.</p>

<p>Ureaformaldehyde is a synthetic slow-release fertilizer that contains urea and formaldehyde. It has been shown to be highly active as a slow-release fertilizer in Langmuir adsorption isotherm studies. Ureaformaldehyde also has the ability to mineralize chloride and hydrogen bond to soil particles, increasing the availability of these ions for plant uptake. Ureaformaldehyde is also used in analytical methods such as chromatographic determination of fatty acids, which are an important component of animal and vegetable oils. !--</p>

<p>Chamigrenal is a complex enzyme that is extracted from the fruit of the chamomile plant, which has been used for centuries in Ayurvedic medicine. Chamigrenal has been shown to have anti-inflammatory and anti-allergic activities. It also binds to G-protein coupled receptors, which may be due to its eluting property. Chamigrenal contains many chemical structures, including phenolic acids, flavonoids, terpenoids, and coumarins. The molecule has been shown to inhibit the growth of human cervical carcinoma cells by binding to a receptor called factor receptor.<br>DEFINITION: Chamigrenal is an extract from the fruit of the chamomile plant that has been used for centuries in Ayurvedic medicine as a treatment for inflammation and allergies. It has also been shown to bind to G-protein coupled receptors and inhibit human cervical carcinoma cells by binding to a receptor called factor receptor.</p>

<p>3,5-Di-tert-butyl-4-hydroxybenzylaldehyde is a compound that can be used as an extraction solvent for solid phase microextraction (SPME) in analytical methods. This sample preparation technique is used to measure the amount of malonic acid in kidney bean samples, as well as to detect growth factors in cell cultures. 3,5-Di-tert-butyl-4-hydroxybenzylaldehyde has been shown to be effective in wastewater treatment and has also been found to have anti-inflammatory properties. In addition, this compound was detected at low levels in urine samples from patients with inflammatory diseases. The mechanism of 3,5-Di-tert-butyl-4-hydroxybenzylaldehyde's antiinflammatory activity may be due to its ability to inhibit oxidative DNA damage by reacting with hydrogen bonds.</p>

<p>4-Acetoxy-3-methoxybenzaldehyde is an antimicrobial agent that is used specifically for the treatment of lemongrass oil and eugenol. It has been shown to be effective against a wide range of microorganisms, such as Escherichia coli, Pseudomonas aeruginosa, Salmonella enterica, Staphylococcus aureus, and Streptococcus pneumoniae. 4-Acetoxy-3-methoxybenzaldehyde has been shown to inhibit the growth of bacteria by binding to the 50S ribosomal subunit. The molecule also has hydroxyl group which can react with potassium dichromate and sodium carbonate. This reaction results in the formation of 4-acetoxy-3-hydroxybenzaldehyde through an S N 2 substitution mechanism.</p>

4-Chloro-2-methylbenzaldehyde is a nucleophilic and electrophilic compound that has a carbonyl group. The vivo model of 4-Chloro-2-methylbenzaldehyde suggests that the methyl groups on the molecule are important for its anti-cancer activities. This compound also has anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. It is used in anti-cancer agents as well as in other applications such as catalysis and synthetic chemistry. 4-Chloro-2-methylbenzaldehyde is synthesized by first reacting benzaldehyde with sodium nitrite, followed by chlorination with phosphorus pentachloride and sodium hydroxide. The mechanistic details of this reaction have not been elucidated yet, but it is believed that the selectivity of this reaction may be due to the presence of aldehydes in the reactants. Further optimization of this reaction would involve changing the

<p>3-Hydroxy-5-nitrobenzaldehyde is a solvent that has been used as a probe to measure chloride concentration in multimedia. It can be used as a sensor and an algorithm to detect the colorimetric change of 3-hydroxy-5-nitrobenzaldehyde in the presence of chloride ions. This probe is also used in colorimetric tests for linker, nonpolar, and surfactant compounds. The 3-hydroxy-5-nitrobenzaldehyde oxime can be cleaved by UV light to produce an unstable nitronium ion that reacts with metal ions such as copper(II) or silver(I) to form an insoluble precipitate.</p>

<p>4-Bromo-3-fluorobenzaldehyde is a drug substance that can be used in cancer therapy. It is a cross-linking agent that can form covalent bonds with DNA and proteins, which inhibits the ability of cells to replicate. 4-Bromo-3-fluorobenzaldehyde has been shown to have cytotoxic activity against human cancer cells in culture. This compound is synthesized by an unsymmetrical nitroaldol reaction, followed by Suzuki coupling with 3-(4′-methoxyphenyl) propanone. The structural formula for this product is C9H5BrFO2.</p>

<p>4-Benzyloxy-3-chlorobenzaldehyde is a chemical intermediate that can be used for the production of a variety of compounds. It is an aromatic compound, with a benzene ring and two oxy groups at each end. The CAS number for 4-benzyloxy-3-chlorobenzaldehyde is 66422-84-2. It is also known as 1,4-dichloroacetophenone. This chemical is useful in the production of speciality chemicals and research chemicals, and it can act as a versatile building block in organic synthesis.</p>

<p>3-Fluoro-4-methoxybenzaldehyde is a chemical compound that is used in the synthesis of natural products. It has been shown to have inhibitory properties against cancer cells, and has been synthesized as an analog of 3-fluoro-4-hydroxybenzaldehyde. The biological function of 3-fluoro-4-methoxybenzaldehyde is not yet known. Hydrochloric acid may be used to react with 3-fluoro-4-methoxybenzaldehyde to form a salt. This chemical also has anti-tumor effects and can be synthesized using cryogenic techniques.</p>

<p>2-Chloro-5-nitrobenzaldehyde (2CNB) is an antibacterial agent that has been shown to be effective against a number of bacterial species. It is a nucleophilic compound and reacts with the sulfhydryl group in cysteine. 2CNB also reacts with the thiol group of proteins, which are involved in many cellular processes. 2CNB has industrial uses, such as for the production of cyclohexanone and cyclopentanone. The structures of 2CNB and its homologues have been studied by 13CNMR spectroscopy, which provides information about the type of bonds present in the molecule and their lengths.</p>

<p>2,4,6-Tribromo-3-hydroxybenzaldehyde (2,4,6-TBHB) is an aldehyde that is synthesized from the reaction of 2,4,6-trichlorobenzaldehyde and bromine. It has been shown to be cytotoxic in tumour cell lines in vitro. This compound binds to DNA by covalent binding and inhibits the synthesis of proteins. 2,4,6-TBHB also inhibits cellular uptake of halides such as chloride and bromide ions. This aldehyde has been shown to induce cell death in human lung cancer cells in a concentration dependent manner.</p>

<p>2-Ethoxybenzaldehyde is an organic compound that has been found to be a potential anticancer agent. It inhibits the growth of tumor cells in vitro, by inhibiting the PI3K/Akt signaling pathway. 2-Ethoxybenzaldehyde also has antibacterial activity against Gram-positive bacteria, such as P. aeruginosa, by binding to the nitrogen atoms on the cell wall and disrupting their function. The molecule has a functional group that reacts with metal cations, which helps to explain its chemical nature and its reaction mechanism. The molecule is soluble in water but not in organic solvents. 2-Ethoxybenzaldehyde crystallizes as a white solid with a monoclinic crystal system and can react with salicylaldehyde to produce benzalmalonic acid.</p>

<p>4,4'-Biphenyldicarboxaldehyde is a n-dimethyl formamide that has been shown to be neuroprotective in animal models of Parkinson's disease (PD). 4,4'-Biphenyldicarboxaldehyde binds to sulfoxide and chloride ions and reduces the hydrophobic effect. This leads to the formation of an imine intermediate. The reaction mechanism is believed to be similar to that of biphenyls, which are used as fungicides. 4,4'-Biphenyldicarboxaldehyde is easily detected by fluorescence analysis and has low toxicity. It is also soluble in organic solvents such as benzene or chloroform.</p>

<p>2,4-Difluoro-3-methylbenzaldehyde is a chemical compound that is used as a building block for the synthesis of other chemicals. It can be used as a research chemical or intermediate due to its versatility. 2,4-Difluoro-3-methylbenzaldehyde has a CAS number of 847502-88-9 and is classified as a speciality chemical with high quality. This compound may be useful in the synthesis of polymers and pharmaceuticals due to its ability to form covalent bonds with other molecules.</p>

<p>2-Hydroxy-4-methoxybenzaldehyde is an antifungal agent that has been shown to have a broad spectrum of activity against filamentous fungi. It is able to inhibit the growth of fungi by inhibiting the enzyme shikimate dehydrogenase, which is involved in the synthesis of aromatic amino acids and other essential metabolites. 2-Hydroxy-4-methoxybenzaldehyde also inhibits xylose reductase and alpha-galactosidase, enzymes that are involved in cell wall biosynthesis. This compound is effective against Candida albicans, Aspergillus niger, and Trichophyton mentagrophytes. 2-Hydroxy-4-methoxybenzaldehyde has also been shown to have bacteriostatic effects on Escherichia coli.</p>

<p>5-Nitrosalicylaldehyde is a powerful inhibitor of bacterial growth. It has been shown to inhibit the growth of gram-positive bacteria such as Staphylococcus aureus and Streptococcus pyogenes, but not gram-negative bacteria such as Escherichia coli. 5-Nitrosalicylaldehyde is an antimicrobial agent that has been shown to bind to the active site of some enzymes, including bacterial DNA gyrase and human liver microsomes. The binding prevents the enzyme from functioning and leads to cell death. 5-Nitrosalicylaldehyde coordinates with sodium ions in the active site, forming strong hydrogen bonding interactions. This interaction stabilizes the transition state for the reaction and prevents it from happening, thereby inhibiting its function.</p>

<p>3-Hydroxy-2-iodobenzaldehyde is a heterocyclic compound that is synthesized from an acetoacetic ester. It is a photochemical precursor to many organic compounds, such as phenanthrene. The synthesis of 3-hydroxy-2-iodobenzaldehyde can be achieved by reacting acetoacetic acid with iodine and sodium nitrite in the presence of a base. This reaction yields 2-iodobenzoic acid in addition to the desired product. 3-Hydroxy-2-iodobenzaldehyde has been studied for its use in the preparation of natural products and research advances.</p>