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<p>3-Methylbenzaldehyde oxime is a fine chemical that can be used as a versatile building block. It has the CAS No. 41977-54-2 and is also known as benzoic acid, 3-methyl-, oxime. 3-Methylbenzaldehyde oxime is a complex compound that can be used in research chemicals and reagents. The chemical has been found to have high quality and is useful for making speciality chemicals and useful intermediates. The compound is also a reaction component for use in synthesis of other compounds. 3-Methylbenzaldehyde oxime can be used as a scaffold for drug design and development.</p>

<p>4-Bromo-3,5-dimethoxybenzaldehyde is a compound that inhibits the replication of cells. It has been shown to induce apoptosis and inhibit tumor growth, including skin tumors and malignant melanoma cells. This chemical is synthesized by reacting an acrylonitrile with sodium hydroxide in a biphenyl amide. 4-Bromo-3,5-dimethoxybenzaldehyde has been used to inhibit bacterial growth, but it is not active against Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>3-Sulfobenzaldehyde sodium salt is a novel anticancer agent that inhibits the activity of HDACs. It has shown a strong inhibitory effect on cancer cells in vivo, and can be used for the treatment of tumors. 3-Sulfobenzaldehyde sodium salt has an anti-proliferative effect on cancer cells, which may be due to its ability to inhibit the activity of HDACs and acetylation mediated by these enzymes. This drug also has an anti-proliferative effect in tumor growth, which may be due to its ability to inhibit the HDAC cycle and acetylation, leading to cell death.</p>

<p>4-Fluoro-2-(trifluoromethyl)benzaldehyde is a chemical compound that can be used as a reagent in the formylation reaction. This product is soluble in ether, chloroform and benzene. The crystallographic data of this product are available and show that it has an isotropic crystal structure with a monoclinic unit cell. The molecular weight of this product is 150.38 g/mol and the molecular formula is C8H6F3O. The wavelength at which maximum absorption occurs for this product is 266 nm.</p>

<p>2-Phenylindole-3-carboxaldehyde is an organic compound that belongs to the class of bioactive molecules. It is a nitrogen heterocycle that has been shown to inhibit the growth of cancer cells in culture. 2-Phenylindole-3-carboxaldehyde has also been shown to have anti-inflammatory and antimicrobial properties. This molecule can be used in the treatment of cancer, as it inhibits the growth of tumor cells by inhibiting DNA synthesis, which leads to cell death. The molecular structure can be altered by allylation or replacement with other functional groups. The 2-phenylindole moiety can be modified at its C2 position, altering its pharmacological properties and may lead to new anticancer drugs.</p>

4-Hydroxybutyraldehyde is a carbonyl group that contains a zirconium oxide fragment. It is acidic and can be used as an inhibitor of tumor cells. 4-Hydroxybutyraldehyde has been shown to deuterium isotope effect on the reaction mechanism. This chemical ionization process leads to the production of an H3+ cation, which reacts with the sample in order to produce a protonated product. The hydrogenated form of this molecule undergoes an addition reaction with butyrolactone, forming the desired product. The synthetic pathway for this molecule starts with metal carbonyl complexes, which react with nucleophiles such as ammonia or amines to produce 4-hydroxybutyraldehyde.

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>2,4-Diaminobenzaldehyde is a chemical compound that is used as an intermediate in the synthesis of drugs and other organic chemicals. It can be oxidized with periodate to produce 2,4-diaminophenol. This reaction system can then be desilyated to produce 2,4-diaminoanisole. Reaction time has a significant effect on the yield of this reaction system. The optimal dosage of periodate for this reaction system is 0.5 mM for 2,4-diaminophenol and 0.1 mM for 2,4-diaminoanisole. This reaction system can also be carried out using lavendamycin or tosyl chloride instead of periodate. The conversion efficiency of this reaction system is dependent on the presence or absence of methyl esters in the starting material and product.<br>END&gt;</p>

<p>2,6-Dihydroxybenzaldehyde is a chemical compound that has been used as an intermediate in the synthesis of other chemicals. It is also used as a precursor for benzaldehyde and benzoic acid. 2,6-Dihydroxybenzaldehyde can be synthesized by reacting sodium carbonate with pluronic F127 in the presence of cationic surfactant. The surface methodology used in this process involves the use of hydrophobic molecules to form micelles and liposomes on the surface of the electrode. The interaction between these micelles and liposomes is pH dependent. This reaction causes an increase in hydrogen ions, which leads to an increase in conductivity at acidic pH values. Electrochemical impedance spectroscopy (EIS) results show that 2,6-dihydroxybenzaldehyde reacts with high concentrations of salt and water vapor. FTIR spectroscopy shows that it has two hydroxyl groups and one double</p>

<p>4-Benzyloxy-3-methoxybenzaldehyde is a deuterium isotope analog of the natural compound benzaldehyde. This molecule has been shown to inhibit the growth of cancer cells in tissue culture by binding to DNA. The molecular mechanism of this inhibition is believed to involve an enzymatic process that results in the substitution of chloride for chlorine, thereby inhibiting DNA synthesis and preventing cell division. 4-Benzyloxy-3-methoxybenzaldehyde also inhibits the production of growth factors and thus has anticancer activity.</p>

<p>5-Bromoindole-3-carboxaldehyde is a water molecule that has been crystallized in the form of an amide. It is a chemical substance with asymmetric synthesis and significant antifungal activity. 5-Bromoindole-3-carboxaldehyde is active against some strains of the fungus Candida albicans and has been shown to inhibit the growth of kidney cells. This molecule also binds to the neurokinin 1 receptor and is used as a probe for fluorescence studies. The efficient method for synthesizing 5-Bromoindole-3-carboxaldehyde includes using silico analysis to confirm the structure on a computer, then performing an asymmetric synthesis with an acid catalyst to produce this compound.</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>2-Heptenal is a fatty acid that is found in small quantities in the human body. It has been shown to inhibit the activity of lipases and esterases, which are enzymes that break down fats. 2-Heptenal can be used as an analog for fatty acids and as a sample preparation agent when preparing fatty acids for analysis. 2-Heptenal has been shown to exhibit degenerative disease properties, such as Alzheimer's disease. Researchers have used 2-heptenal as a model system to study the aggregation process of amyloid proteins, which may lead to the development of drugs for treatment of these diseases.</p>

<p>3-Ethoxy-4-hydroxybenzaldehyde is an active analogue of p-hydroxybenzoic acid that can be used in the synthesis of vanillin. 3-Ethoxy-4-hydroxybenzaldehyde is extracted from a reaction solution using solid phase microextraction, and can then be analyzed by gas chromatography/mass spectrometry to determine the concentration of vanillin. This compound has been shown to have a solubility in water, but not in organic solvents. 3-Ethoxy-4-hydroxybenzaldehyde has been found to inhibit cytochrome P450 activity and polyvinyl chloride production. This chemical compound has also been found to be toxic when inhaled or ingested, with no known toxicity studies for skin contact or eye contact.</p>

3-Fluoro-4-hydroxybenzaldehyde is a hydroxyl group with an activation energy of 87.7 kJ/mol. The molecule can be synthesized by the reaction of salicylaldehyde and 3,4-dihydroxybenzaldehyde in the presence of an organic solvent such as chloroform or methylene chloride. This compound has been shown to cause cell death in ht-29 cells and cancer cell lines, as well as human ovarian carcinoma cells. It causes apoptosis by inhibiting mitochondrial membrane potential, which leads to decreased intracellular ATP levels. 3-Fluoro-4-hydroxybenzaldehyde is most commonly used in molecular modeling studies to represent the hydroxyl group due to its simplicity in comparison to other hydroxyl groups like methanol or ethanol.

<p>3-Chloro-4-nitrobenzaldehyde is an aldehyde that is produced by the oxidation of 2-chloro-4-nitrobenzaldehyde. This chemical has been shown to have antitubercular activity in human erythrocytes, and it can be recycled from its reaction product with sodium hypochlorite. 3-Chloro-4-nitrobenzaldehyde has been shown to interact with acidic heterocycles such as oxadiazoles and triazoles. 3-Chloro-4-nitrobenzaldehyde has also been shown to alter the morphology of bacteria, such as subtilis, when exposed to ionic liquids. It is also known to inhibit the growth of Gram positive bacteria and show cytotoxic effects on mammalian cells.</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>

o-Anisaldehyde is a chemical compound that has the molecular formula CH3CHO. It is an aromatic compound that contains a hydroxyl group (-OH) bonded to a benzene ring. o-Anisaldehyde is soluble in water and reacts with copper chloride to form copper (II) o-anisate, which can be used as a reagent for oxidation reactions. It also forms coordination compounds with metal ions like zinc and iron. The crystal structure of o-anisaldehyde has been determined by x-ray crystallography and shows that it contains two asymmetric carbon atoms, which are oriented in opposite directions. This molecule can be synthesized from phenol or catechol by heating them with an acidified solution of sodium nitrite in ethanol. The reaction mechanism of this process involves the formation of an oxime intermediate followed by hydrolysis. The kinetics data of this reaction have been obtained using titration calorimetry and kinetic energy measurements show that the reaction

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>3-Methoxybenzaldehyde is a chemical compound that is used as an intermediate in the synthesis of organic compounds. This compound has shown to be a potent inhibitor of several enzymes, including diamine tetraacetic acid (DAT)-dependent aminotransferase, trimethyl amine N-oxide reductase, and hydrochloric acid hydrolases. 3-Methoxybenzaldehyde also inhibits the growth of hepg2 cells and induces apoptosis. The chemical structure of this compound contains a boron nitride group that can form hydrogen bonds with other molecules and fatty acids that can act as a substrate for oxidation reactions.</p>

<p>4-Ethoxy-3-methoxybenzaldehyde is an organic compound that can be found in plants, such as in the leaves of the nutmeg plant. It is a cleavage product of 4-hydroxycoumarin. 4-Ethoxy-3-methoxybenzaldehyde is a dicarboxylic acid by substructure and it has been shown to be an intermediate in the synthesis of ethylene acetal and hydrogen peroxide. It is also postulated to react with chloride to form 4-chloroacetophenone and chloride ions, which are then reacted with hydrogen peroxide to form hydrochloric acid. The acute toxicity of this compound has not been determined but it may cause toxic effects on extracellular cells, such as radical species. The toxicities of 4-ethoxy-3-methoxybenzaldehyde have been observed in biphenyl which causes skin irritation, liver toxicity, kidney damage, and respiratory irritation</p>

<p>When used in combination with X-Gal, 4-dimethylamino-2-methoxybenzaldehyde can be used for effective staining under anaerobic conditions. This novel method is termed Indoxyl/Dimethylamino-2-methoxybenzaldehyde aldol staining and can be used as an alternative to indoxyl-substrate indicator systems which depends on molecule oxygen to develop the desired indigo chromogen.</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>

3-Nitro-6-pyridinecarboxaldehyde is a colorless liquid that is soluble in water. It has a boiling point of 155 degrees Celsius, and it has a density of 1.03 grams per milliliter. This chemical reacts with metal ions to form nitro compounds. 3-Nitro-6-pyridinecarboxaldehyde has been used as an analytical reagent for the determination of benzenes and pyridines in organic solvents and gas chromatography calibration. The reactivity of this chemical is due to its pyridine ring, which can be used as a ligand or reagent.

Z-Phe-Tyr-aldehyde is a natural compound that inhibits the activity of cathepsin, an enzyme associated with cancer and bowel disease. The compound also inhibits the expression of covid-19, which is a protein that regulates cell death. Z-Phe-Tyr-aldehyde has been shown to cause caspase-independent cell death in human leukemia cells. This compound also blocks the TLR4 receptor, which is thought to play a role in infectious diseases such as SARS and Covid-2. It has been found to inhibit protein synthesis in bacteria, which may be due to its ability to inhibit ribosomal function.

<p>3-Hydroxy-2-methoxybenzaldehyde is a synthetic compound that is used as an antiviral agent. It has been shown to inhibit the replication of Coxsackievirus A9 (CV-A9). In addition, 3-Hydroxy-2-methoxybenzaldehyde reacts with isoeugenol and isonicotinic acid under acidic conditions to form 4-allyl-2-methoxyphenol, which has antiviral activity against CV-A9. This reaction requires a catalyst, such as zinc chloride or nickel sulfate. The rate of this reaction can be increased by increasing the reaction time. 3-Hydroxy-2-methoxybenzaldehyde also inhibits the virus's ability to bind to cells and enter them, reducing its infectivity.</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>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>Intermediate in organic synthesis</p>

<p>2,6-Dimethyl-4-fluorobenzaldehyde is a fine chemical that is used as a building block in the synthesis of other chemicals. It can be used as a reagent and as a speciality chemical. This product has high purity and quality and is versatile in its use as both an intermediate or scaffold molecule. It can be used in reactions to create complex compounds with useful properties.</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>3,5-Dichloro-4-hydroxybenzaldehyde is a triiodomethane derivative that reacts with chlorine to form a chlorinated aldehyde. It is used as an intermediate in the production of 4-hydroxybenzoic acid from phenylacetic acid and 4,4'-dichlorodiphenyl sulfone. 3,5-Dichloro-4-hydroxybenzaldehyde can be decarboxylated at elevated temperatures to produce formic acid. This compound has been used in wastewater treatment as it can remove chlorine byproducts and other pollutants such as nitrates, nitrites, and iron ions. The reaction kinetics of 3,5-dichloro-4-hydroxybenzaldehyde have been studied using hydroxymethyl groups and formyl groups to determine the rate of demethylation. The rates were found to be dependent on temperature.</p>

<p>4-Benzyloxy-3,5-dimethylbenzaldehyde is a potent anticancer drug that inhibits cell proliferation and induces apoptosis. It has been shown to inhibit the growth of prostate cancer cells and human erythroleukemia cells. This compound also has antibacterial activity against gram-positive bacteria such as methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. 4-Benzyloxy-3,5-dimethylbenzaldehyde binds to the flavone binding site on the enzyme DNA gyrase and topoisomerase IV in both bacterial and mammalian cells. This binding leads to inhibition of DNA synthesis by preventing the formation of an enzyme complex with DNA polymerase. A study has shown that apigenin, one of the flavone derivatives found in this compound, enhances the antitumor activity of cisplatin by inhibiting DNA repair mechanisms in human cancer cells.</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>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>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>

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>5-Cyanoindole-3-carboxaldehyde is an aldehyde that is used in synthesis of β-unsaturated aldehydes. It is prepared by the reaction of 3-cyanoindole with formaldehyde. 5-Cyanoindole-3-carboxaldehyde has antibacterial activity against gram positive and gram negative bacteria. It also has a high yield and can be purified by filtration or by condensation with chlorobenzene. 5-Cyanoindole-3-carboxaldehyde can be activated by irradiation, which makes it useful for the production of pharmaceuticals.</p>

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>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>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>2,4-Difluorobenzaldehyde is a glycosidic bond compound that is chiral. It has been shown to be able to inhibit human immunodeficiency virus (HIV) infection and inflammatory bowel disease. 2,4-Difluorobenzaldehyde is also an inhibitor of cholesterol ester transfer protein that can lead to autoimmune diseases. This compound has been shown to have receptor activity and is synthesized by the reaction of 2,4-dichlorobenzaldehyde with dimethyl acetal in refluxing ethanol. The synthesis method for this compound involves synchronous fluorescence and radiations. 2,4-Difluorobenzaldehyde has been found to have anti-inflammatory properties due to its ability to inhibit chronic pulmonary inflammation in rats.</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>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-Naphthaldehyde oxime is a reactive aldoxime that can be used as an oxidant in organic chemistry. It is able to increase the rate of hydrolysis by acid catalysts, and has been shown to cause biomolecular damage due to its ability to react with functional groups such as amines and alcohols. 2-Naphthaldehyde oxime reacts with silicon, styrene, and polystyrene. The reaction produces carbon dioxide, hydrogen, and water. This product also has the capability of solvating organic compounds through the use of water molecules. Hypervalent oxidation reactions may occur with 2-naphthaldehyde oxime due to its ability to form multiple bonds with oxygen atoms.</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>

4-(Trifluoromethoxy)benzaldehyde is a chemical compound that is a substrate for tyrosinase and an inhibitor of the enzyme. It is also an anticancer compound that can be used to inhibit tumor growth by inhibiting protein synthesis. 4-(Trifluoromethoxy)benzaldehyde has been shown to have potent tyrosinase inhibition activity in vitro and in vivo, as well as binding activities with the CB2 receptor. This chemical has also been shown to inhibit virus replication, including HIV-1, and tuberculosis. 4-(Trifluoromethoxy)benzaldehyde can be used in assays to measure the potency of other compounds that are involved in tyrosinase activity or have anti-cancer properties. 4-(Trifluoromethoxy)benzaldehyde specifically binds to residues in the kinase domain of the enzyme tyrosinase, which is responsible for catalysis and regulation of this enzyme.

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. 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>Benzo[b]thiophene-2-carboxaldehyde is a compound that has optical properties with a dihedral angle of 90°. This compound also has a functional group of imine, which can be found in the amino acid histidine. Benzo[b]thiophene-2-carboxaldehyde has been shown to have cancer inhibiting properties by targeting the protease activity of at1 receptors. It inhibits the synthesis of protein and RNA by binding to them and preventing their production. This compound also inhibits the activity of proteases, which are enzymes that break down proteins. Benzo[b]thiophene-2-carboxaldehyde is synthesized through metathesis reactions, which are reactions that involve the exchange of atoms between two compounds. The yield is isolated at about 95%.</p>

<p>3,5-Dimethylbenzaldehyde oxime is a white crystalline solid that is soluble in organic solvents. 3,5-Dimethylbenzaldehyde oxime reacts with water to produce hydrogen peroxide and formaldehyde. This reaction is an example of a dehydration reaction.</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>L-Adrenaline is a hormone that belongs to the group of nonsteroidal anti-inflammatory drugs. It is used in combination therapy for the treatment of asthma, chronic obstructive pulmonary disease and other respiratory diseases. L-Adrenaline has also been shown to increase blood pressure and heart rate. L-Adrenaline may interact with other medication such as cardiac glycosides and calcium channel blockers, so it is important to consult with a doctor before taking this drug. L-Adrenaline is a potent vasoconstrictor that can cause primary pulmonary hypertension, which can lead to heart failure. The epinephrine in this drug binds to receptors on cells in the lungs, increasing bronchial secretions, which reduces the symptoms of anaphylaxis.</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>

4-(Dimethylamino)benzaldehyde (4DMAB) is an analytical reagent used to identify sulfa drugs. It has been shown to react with sulfonamides by the formation of a complex ion, which can be detected by analytical methods such as electrochemical impedance spectroscopy or ultraviolet spectroscopy. 4DMAB has also been studied for its anticarcinoid properties. The carcinoid syndrome is characterized by a tumor that releases serotonin and other substances into the bloodstream, causing severe diarrhea, flushing, and bronchial spasms. Studies have shown that 4DMAB inhibits the release of serotonin in this condition. As a result, it may be effective against carcinoid syndrome.

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.

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>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>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>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>

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.

2-Chloro-4-hydroxybenzaldehyde is a potent competitive inhibitor of serine proteases, including thrombin. It also has an anticoagulant effect and can be used as an anti-cancer agent. 2-Chloro-4-hydroxybenzaldehyde has been shown to have a strong affinity for the progesterone receptor, which is a protein that regulates the activity of progesterone in cells. 2-Chloro-4-hydroxybenzaldehyde also binds to the formyl group of phenols and quinones, which leads to its use as an antioxidant in various applications. This compound is found in environmental pollution, where it can chelate metal ions such as chloride and lead.

<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>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>2-Nitroterephthalaldehyde is a chiral molecule that can be used in the supramolecular synthesis of macrocycles. This molecule has been shown to catalyze the formation of imines, which are important for the synthesis of macrocycles. The kinetic and thermodynamic properties of 2-Nitroterephthalaldehyde have been studied and found to be favorable for this type of reaction.</p>

<p>3,4-Dimethylbenzaldehyde oxime is a reactive oxygen species (ROS) that is produced by the oxidation of 3,4-dimethylbenzaldehyde. It has been shown to be an efficient oxidant in aerobic oxidation reactions. The active species generated by this reaction is the aldehyde or ketone form of 3,4-dimethylbenzaldehyde oxime, which can then react with another substrate to generate an oxidized product. This reaction is catalyzed by metal ions and is activated by molecular oxygen.</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>

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<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>

3-Hydroxy-4-methoxy-2-nitrobenzaldehyde is a ternary complex that has been adsorbed onto the surface of an ion exchange resin. The adsorption process occurs through the formation of hydrogen bonds between the hydroxyl groups on the resin and the hydroxyl groups on the molecule. This complex is also soluble in chloroform, which may be due to its ability to form hydrogen bonds with itself and other molecules. The 3-hydroxy group on this molecule has been shown to react reductively with nitrophenol, forming a nitroso derivative. 3-Hydroxy-4-methoxy-2-nitrobenzaldehyde has been used as a template for the microbiological assay of azides and quinones.

<p>Isoprenaline is a hormone that belongs to the category of catecholamines. It is a naturally occurring compound and has been used in medicine as an injectable medication for over 50 years. Isoprenaline is used primarily to treat bronchial asthma, but it also may be used to treat cardiac arrest and heart failure. The drug works by binding to the beta-adrenergic receptors in the lungs, heart, and fat cells. This binding stimulates the production of cyclic adenosine monophosphate (cAMP) in these tissues, which relaxes smooth muscle cells and increases their rate of metabolism. As a result, airways open up due to decreased constriction and increased bronchial secretions are cleared away. The drug also has been shown to have beneficial effects on adipose tissue and structural heart disease.</p>

<p>2,5-Dimethylbenzaldehyde is a chemical that is used in the synthesis of various compounds. It has been shown to have anticancer and energy metabolism properties. 2,5-Dimethylbenzaldehyde can be used as an energy source in the mitochondria. This compound also prevents the formation of fatty acids by inhibiting the conversion of acetyl-CoA into malonyl-CoA. The phase transition temperature for 2,5-dimethylbenzaldehyde is approximately −20 °C. The reaction mechanism for this compound is not well understood, but it has been shown to react with piperonal to form 3,4-dimethylbenzyl alcohol and methyl ethyl ether, which are both carcinogenic compounds. Chemical ionization mass spectrometry experiments have shown that protonated 2,5-dimethylbenzaldehyde reacts with methane gas to form methyl ethane and hydrogen gas. Thermodynamic data suggest that 2,5-dimethyl</p>

<p>L-Noradrenaline is the major precursor of norepinephrine, a neurotransmitter that regulates blood pressure and heart rate. L-Noradrenaline bitartrate monohydrate is a potent vasopressor drug that has been shown to increase blood pressure. The effects in animals are biphasic, with an initial pressor phase followed by a second phase with vasodilator effects. L-Noradrenaline bitartrate monohydrate has been shown to stimulate transcription of proteins, such as model protein and dopamine receptor D1 (D1R). This stimulation has been shown to be mediated through the activation of protein kinase C (PKC) and Ca2+/calmodulin-dependent protein kinase II (CaMKII). It has also been shown to have antioxidant effects in the presence of hydroxyl radicals. L-Noradrenaline bitartrate monohydrate can cause symptoms such as nausea, vomiting, and diarrhea in humans at high doses.</p>

<p>Enalaprilat is an angiotensin-converting enzyme (ACE) inhibitor that prevents the formation of angiotensin II, a potent vasoconstrictor. It is used to treat high blood pressure and congestive heart failure. Enalaprilat is metabolized to enalapril, which has been found to act as an active inhibitor of DNA polymerase. This drug is also capable of inhibiting the synthesis of other proteins, such as those involved in protein transport and cell wall biogenesis.</p>

<p>Echinatin is a benzaldehyde derivative that is found in the roots of Echinacea purpurea. It is a phenolic compound with a carbonyl group and two benzyl groups. 4-Hydroxy-2-methoxybenzaldehyde has been shown to have photophysical, cell culture, and functional group properties. This compound is used as a precursor for the production of echinatin and other plant polyphenols such as malonic acid. The biosynthesis of 4-hydroxy-2-methoxybenzaldehyde begins with the oxidation of cinnamic acid by cytochrome P450 monooxygenase to form cinnamoyl CoA. The enzyme cinnamate decarboxylase then converts this intermediate to p-hydroxybenzoic acid, which is then hydroxylated to form 4-hydroxy-2-methoxybenzaldehyde.</p>

<p>2-Bromobenzaldehyde is an important aryl aldehyde that can be synthesized through the copper-catalyzed coupling of 2-bromobenzyl bromide and phenylacetone. The synthesis of 2-bromobenzaldehyde has been used to study the effects of physiological activities on the coordination geometry. It is also used as a fluorescent probe for amines and esters, which are commonly found in bioinorganic chemistry. The compound is characterized by intermolecular hydrogen bonding and hydrogen bonding between the hydroxy group and chloride, which are associated with its acidity.<br>2-Bromobenzaldehyde has been shown to have antiinflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>1H-Pyrrole-2-carbaldehyde is a compound that belongs to the class of ferrocenecarboxylic acids. It is a coordination complex with a pyrrole system and an intramolecular hydrogen bond. The proton on the carbonyl carbon atom forms hydrogen bonds with nitrogen atoms, which are located in the immediate vicinity of the carbonyl group. The structure was determined by x-ray diffraction studies and the reactivity was studied by means of X-ray crystal structures. This compound has been used for biological studies as well as for structural analysis.</p>

<p>4-(N,N-Diethylamino)salicylaldehyde is a coumarin derivative that has been shown to be a fluorescent probe for proton transfer. It emits light at around 400 nm when the probe is excited by light of wavelength greater than 300 nm. The emission spectrum changes from green to red as the pH increases. 4-(N,N-Diethylamino)salicylaldehyde also exhibits fluorescence enhancement in the presence of metal ions such as Fe3+, Cu2+, or Cr3+. This compound can be used as a fluorescent probe for hydrogen bonding interactions and metal hydroxides.</p>

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<p>4-Isopropoxybenzaldehyde is a synthetic compound that belongs to the group of lipopolysaccharides. It is a photophysical and voltammetric study of wastewater, which was found to be an effective halide scavenger. 4-Isopropoxybenzaldehyde has been shown to have high antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. This compound also has acute toxicities when administered to animals. The toxicity may be due to its ability to inhibit protein synthesis as well as other cellular processes.</p>

3-Methoxy-4,5-methylenedioxybenzaldehyde (MMDA) is an amine that is used in the synthesis of drugs and pharmaceuticals. It is a major component of myristicin, which is found in nutmeg. MMDA can be synthesized from aluminium chloride, hydrochloric acid and pyridine. The molecule has a skeleton that is recemic at acidic pH values and mesoionic at basic pH values. This compound also reacts with acetyl chloride to form 3,4-dimethoxyacetophenone, which can be chromatographically separated from other compounds. The chromatography produces flavonoid derivatives such as quercetin, 3′-methoxyquercetin and 3′,4′-dimethoxyquercetin. Flavonoids are polyphenolic compounds found in plants that have antioxidant properties. Chromatographic separation of these compounds can be done using spectrometric methods to