Aldehídos

<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>3,5-Dibromobenzaldehyde is an analytical reagent that has been used as a chemosensor. The compound was synthesized by the reaction of benzaldehyde with bromine and potassium hydroxide (KOH). 3,5-Dibromobenzaldehyde has a skeleton consisting of three phenyl groups and two aldehyde groups. The compound also contains two active methylene groups and two vinylene groups. 3,5-Dibromobenzaldehyde can be detected by fluorescence probe or low energy electron diffraction. This chemical is an effective antibacterial agent with an LD50 value of 1.6 milligrams per kilogram in rats.</p>

<p>Mesitaldehyde is a diazonium salt that is synthesized by the reaction of nitrosyl chloride and sodium carbonate in an acidic solution. This chemical has been studied for its potential use as a therapeutic drug due to its ability to inhibit the enzyme dpp-iv, which is involved in the development of diabetic neuropathy. Mesitaldehyde has also been shown to be an inhibitor of malonic acid, ethylmalonic acid and other organic acids. The analytical method for mesitaldehyde involves hydrolyzing the product with hydrochloric acid in order to produce ethylmalonic acid, which can then be quantified using spectrophotometry.</p>

<p>4-N-Octylbenzaldehyde is a nitro compound which is used as an immunosuppressive agent. It has been shown to inhibit the activity of diphenolase, which plays an important role in the metabolism of fatty acids. 4-N-Octylbenzaldehyde also has an oil extractant that can be used to extract and separate different types of organic compounds from oils, fats, or greases. In addition, 4-N-octylbenzaldehyde inhibits the synthesis of prostaglandin E2 and thromboxane A2 by inhibiting cyclooxygenase enzymes. It has been shown to possess anti-inflammatory properties and has been found to be useful in treating rheumatoid arthritis.</p>

4-Methoxy-2-(trifluoromethyl)benzaldehyde is a chemical that has been used in the synthesis of a variety of compounds. It is an important intermediate for the production of pharmaceuticals, agrochemicals, and fine chemicals. This compound can be used as a building block to produce other organic compounds with high quality. 4-Methoxy-2-(trifluoromethyl)benzaldehyde can also be used as a reagent in organic chemistry reactions, such as the synthesis of indoles. The CAS number for this compound is 106312-36-1.

<p>3-Chloro-2-nitrobenzaldehyde is an analog of 2-nitrobenzaldehyde. It can be synthesized by reacting a halogen with benzaldehyde, such as chlorine or bromine. 3-Chloro-2-nitrobenzaldehyde is unreactive and can be used in the production of other compounds, such as pharmaceuticals. 3-Chloro-2-nitrobenzaldehyde has been shown to react with sodium methoxide to produce a methoxide. The methoxide is then reacted with an alcohol to produce an ester.</p>

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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>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>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>

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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>

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.

<p>3-Hydroxybenzaldehyde (3HBA) is an organic molecule that belongs to the group of substituted benzaldehydes. It has been shown to induce muscle cell proliferation in vitro and in vivo, as well as increased levels of activated caspase-3 in vitro. 3HBA also has a high resistance to hydrochloric acid, hydrogen bond, and chemical structures. It also shows properties of intramolecular hydrogen bonding and aldehyde groups. 3HBA has been shown to be active against malonic acid-induced pulmonary edema in rats, which may be due to its ability to inhibit the release of erythrocytes from the bone marrow into the circulation.</p>

<p>2,4-Dimethylbenzaldehyde is used in the diagnosis of cancer. It reacts with acetaldehyde to form a compound that binds to hemoglobin and is excreted in the urine, leading to a diagnostic test for cancer. 2,4-Dimethylbenzaldehyde has been shown to be genotoxic in both in vitro and in vivo studies. This aromatic hydrocarbon has been shown to cause DNA strand breaks in the target cells through a reaction mechanism involving radical formation from acetaldehyde. In addition, 2,4-Dimethylbenzaldehyde has been shown to have genotoxic effects on mice exposed by inhalation or injection.</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>3-Chloro-4-hydroxybenzaldehyde is a molecule that belongs to the class of aldehydes. It is a monocarboxylic acid and an important precursor in the production of coumarin derivatives. 3-Chloro-4-hydroxybenzaldehyde has been shown to have pharmacokinetic properties, such as vibrational, chemical, and optical properties. It is also a fluorophore with strong fluorescence emission. The hydroxymethyl group can be programmed by adding an amine or thiol group at the 4 position on the ring of 3-chloro-4-hydroxybenzaldehyde. The addition of these groups will change the optical properties of 3-chloro-4-hydroxybenzaldehyde to make it more useful for biotechnology applications.</p>

2-Carboxy-3,4-dimethoxybenzaldehyde is a chemical that belongs to the class of compounds known as butyric acid derivatives. It is a colorless liquid with a pungent odor and can be used in pharmaceutical preparations as an antispasmodic or a sedative. 2-Carboxy-3,4-dimethoxybenzaldehyde has been shown to have radical scavenging activities in tissue culture systems and dry weight reaction products in the presence of hydrochloric acid and chloride ion. This compound can also act as an acid complexing agent for hydrogen chloride and depressant activity on animal behavior.

<p>2-Benzyloxy-3-methoxybenzaldehyde is an enantiopure compound that has been shown to have antiproliferative effects on cancer cells. It was also found to have a strong binding affinity for DNA and protein. The antiproliferative effects of 2-Benzyloxy-3-methoxybenzaldehyde were found to be due to its ability to bind to dna and inhibit the enzyme activity of pyrazine-2-carboxylic acid, leading to a decrease in the production of proteins vital for cell division. 2-Benzyloxy-3-methoxybenzaldehyde has been shown to have anticancer activity against colorectal cancer cells and may serve as a lead compound for future drug development.</p>

<p>2,6-Dimethoxy-4-methylbenzaldehyde (DMMB) is a useful chemical that is used as a building block in the synthesis of complex compounds. It has been shown to be an effective chemical intermediate and can be used in the synthesis of various products, such as pharmaceuticals and pesticides. DMMB can also be used to produce high quality research chemicals.</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-Fluoro-6-nitrobenzaldehyde is an electron donor that reduces a range of electron acceptors including piperazine. This compound has been shown to have antitumor effects. 2-Fluoro-6-nitrobenzaldehyde has also been shown to inhibit the growth of cancer cells in vitro and in vivo. The mechanism of action is not yet known, but it is thought that 2-fluoro-6-nitrobenzaldehyde may be a potential chemotherapeutic agent for pancreatic cancer therapy.</p>

<p>β-adrenoreceptor agonist; betamimetic agent</p>

2-Nitrobenzaldehyde is a nitro compound that reacts with the intramolecular hydrogen of an alkene to form a nitroalkane. It is used as an antimicrobial agent, in which it inhibits the growth of bacteria by reacting with the intermolecular hydrogen bonding in the bacterial cell membrane. In addition, 2-Nitrobenzaldehyde has been shown to inhibit fatty acid synthesis and transfer reactions. The optimum concentration for this chemical is 0.01% to 0.1%. This chemical is soluble in both water and organic solvents, such as methanol and ethanol.

4-Hydroxy-3-methylbenzaldehyde is a fungicidal agent that has been shown to have activity against Cryptococcus neoformans. It inhibits the mitochondrial functions of this fungus, which leads to cell death by disrupting the synthesis of fatty acids and other cellular components. 4-Hydroxy-3-methylbenzaldehyde binds to C. neoformans with high affinity, producing a reaction product that interferes with the organism's ability to produce butyric acid. The molecular modelling of this compound shows that it is a pyrazole ring with two benzyl groups on either side of an aldehyde group. This chemical also inhibits gram-negative bacteria by binding to fatty acids in their outer membrane.

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>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>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>Pyruvic aldehyde is a reactive compound that is an intermediate in the glycolytic pathway. It is used in vitro to measure enzyme activities and as a model system for studying pathogenic mechanisms. Pyruvic aldehyde has been shown to damage mitochondrial membranes by increasing the production of reactive oxygen species, leading to the collapse of mitochondrial membrane potential and cell death. The methylglyoxal-derived compound also has pharmacological effects, such as anti-inflammatory activities. Pyruvic aldehyde can be prepared using preparative high-performance liquid chromatography (Hplc) or by reacting pyruvate with acidified ethyl acetate.</p>

<p>2,4-Dihydroxybenzaldehyde (2,4DBA) is a copper complex that has been shown to have biological properties. This compound has been studied in biological studies and is classified as group p2 on the periodic table. It is a redox potential of -0.95 V and can undergo intramolecular hydrogen bonding with itself or with other molecules to form hydrogen bonds. Hydroxyl groups are found on 2,4DBA and can coordinate with the nitrogen atoms found on penicillin-binding proteins or acetylcholinesterase inhibition. The coordination geometry of 2,4DBA is tetrahedral and its methyl ethyl group is also found on this molecule.</p>

<p>5-Iodo-2,3-dimethoxybenzaldehyde is a fine chemical that is useful as a scaffold for the synthesis of other compounds. It can be used as an intermediate for research chemicals or as a reaction component in the synthesis of complex compounds. 5-Iodo-2,3-dimethoxybenzaldehyde is used for the manufacture of high quality reagents and building blocks.</p>

<p>2-Hydroxy-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]benzaldehyde is a reaction component that is used in the synthesis of organic compounds. It has been shown to be an effective reagent and can be used in the synthesis of high quality compounds. CAS No. 308085-25-8, it is a research chemical that can be used as a useful scaffold or building block for other compounds. 2-Hydroxy-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]benzaldehyde may also be useful as an intermediate or building block in complex synthesis reactions.</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>Synthetic building block</p>

<p>2-(3,4-Dimethoxyphenyl)acetaldehyde is a bioactive molecule that has shown anti-cancer properties in vitro and in vivo. It inhibits the activity of aldehyde dehydrogenase, an enzyme responsible for the oxidation of alcohols to aldehydes. This inhibition leads to accumulation of acetaldehyde in cells and induces apoptosis or cell death by caspase-independent mechanisms. 2-(3,4-Dimethoxyphenyl)acetaldehyde also has been shown to induce acidolysis reactions in the presence of acid. This reaction mechanism may be due to protonation of the phenolic hydroxyl group. The resulting 3,4-dimethoxyphenylacetic acid analog can inhibit cells' proliferation and induce apoptosis by blocking protein synthesis and cell division.</p>

4'-Chloro-[1,1'-biphenyl]-4-carbaldehyde (CBA) is an intermediate in the synthesis of oritavancin. CBA is obtained by condensation of benzyl chloride and aldehydes. It is also used as a precursor to other compounds. In the laboratory, it can be obtained by heating an ether with chloroform in the presence of acid. 4'-Chloro-[1,1'-biphenyl]-4-carbaldehyde has been shown to be toxic, selective and efficient for certain reactions.

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

2,4,6-Trimethoxy-3-methylbenzaldehyde is a flavanone that is structurally related to the drug ciprofloxacin. The two molecules share a common molecular framework with the addition of a hydroxyl group on the 2 position of the benzene ring. In molecular docking studies, 2,4,6-Trimethoxy-3-methylbenzaldehyde has shown antitubercular activity against Mycobacterium tuberculosis and Mycobacterium avium complex. It is also an inhibitor of protein tyrosine phosphatase and has been shown to have antibacterial activity against various strains of bacteria.

<p>5-(Trifluoromethoxy)salicylaldehyde is a ligand that binds to the active site of the enzyme catalysis, thereby inhibiting its activity. It has been shown to be effective in colon cancer and other cancers due to its ability to inhibit protein synthesis. 5-(Trifluoromethoxy)salicylaldehyde also inhibits the production of prostaglandins, which may prevent inflammation. The compound is also used in supramolecular chemistry and biological studies as a tool for studying protein-ligand interactions. 5-(Trifluoromethoxy)salicylaldehyde has been shown to have dose-dependent effects on cell proliferation and protein synthesis.</p>

4-Biphenylcarboxaldehyde is a chemical compound that belongs to the group of hydrocarbons. It is a colorless liquid with an unpleasant odor, soluble in ether and benzene, and has a boiling point of 210 °C. 4-Biphenylcarboxaldehyde can be used as a raw material for the production of pharmaceuticals and agrochemicals. The molecular structure of this compound is unsymmetrical due to its biphenyl backbone and two carbonyl groups. Hydrochloric acid reacts with 4-biphenylcarboxaldehyde to form 2-bromoethylbenzene and hydrogen gas:

<p>2-Hydroxy-4-nitrobenzaldehyde is a molecule that reacts with kinase receptors in cancer cells and causes oxidative carbonylation. It has been shown to react with chloride, salicylaldehyde and dobutamine to form a fluorescent compound, which can be used as a probe for fluorescence studies. The fluorescence properties of 2-hydroxy-4-nitrobenzaldehyde have also been exploited for the development of pyrazoles as potential anti-cancer agents.</p>

<p>2,4-Dichloro-5-fluorobenzaldehyde (2,4-DFCA) is a functional group that can be found in inorganic, fatty acids, and fatty acid. 2,4-DFCA has been shown to increase insulin-like growth factor I (IGF-I) levels in vitro and in vivo. 2,4-DFCA also increases the expression of IGF-I gene polymorphisms. This compound is used to induce insulin resistance by increasing serum level of IGF-I. 2,4-DFCA also inhibits the activity of a protein called impeller that is required for cardiac contractility. This compound can be found on the surface of untreated control cells.</p>

2,4-Dimethoxy-6-methylbenzaldehyde is a biomolecular that belongs to the class of depsidones. It is a tetracyclic compound that has been isolated from the fungus Antrodia camphorata and the lichen Xanthoria polycarpa. 2,4-Dimethoxy-6-methylbenzaldehyde has been shown to inhibit the growth of fungi by preventing oxidative phosphorylation in mitochondria. This compound also shows regioselectivity for phenanthrenes, which are aromatic hydrocarbons with two benzene rings and one or more methyl groups on each ring. The synthesis of 2,4-dimethoxy-6-methylbenzaldehyde is achieved through a Witting reaction between olefinic compounds and diethyl malonate in the presence of base. 2,4-Dimethoxy-6-methylbenzaldehyde can also be synthesized by oxidizing dib

<p>Glycolaldehyde dimer is a molecule that is the product of an intramolecular hydrogenation reaction. It has been shown to have estrogen receptor modulator activity, which may be due to its ability to bind to estrogen receptors and inhibit the production of inflammatory cytokines. Glycolaldehyde dimer also has the potential to be used as a therapeutic agent for inflammatory bowel disease. Glycolaldehyde dimer binds to crystalline cellulose and undergoes a series of chemical reactions, including hydrolysis by hydroxyl group, hydrochloric acid, and hydrogen bond. The logistic regression analysis shows that the molecule is more potent in rats with bowel disease than those without.</p>

5-Acetoxymethyl-2-furaldehyde is a furanic acid that is found in the plant Triticum aestivum. This compound has been shown to have antifungal and anticancer properties. 5-Acetoxymethyl-2-furaldehyde inhibits the growth of bacteria by forming a complex with p-hydroxybenzoic acid, which prevents the formation of amines. The toxicity of this compound may also be due to its ability to cause DNA damage, leading to cell death. 5-Acetoxymethyl-2-furaldehyde can be used as an oxidation catalyst for reactions involving amines. It can also be produced by oxidizing 2,5 furanone with hydrogen peroxide and hydrochloric acid at high temperatures. The reaction mechanism is not well understood but it is believed that 5 acetoxymethyl - 2 furaldehyde is formed from the dehydration of furfuraldehyde.

<p>4-Benzofurazancarboxaldehyde is a pyridinium salt that has been shown to be an oxidant and primary amine. It can form a benzoxadiazole or benzothiadiazole with the addition of an amine, such as piperidine. 4-Benzofurazancarboxaldehyde is also able to form a methyl ester with alkali metal. This compound has been shown to have high yield in the formylating reaction.</p>

<p>3-Hydroxy-2,2-dimethylpropanal is a condensation product of formaldehyde and glycol. It is the simplest of the three aldehydes that are produced by this reaction. The catalyst for this reaction is usually dibutyltin oxide, which can be replaced with calcium chloride or sodium carbonate. 3-Hydroxy-2,2-dimethylpropanal reacts with neopentyl glycol to form a dimer and glycol ester. This reaction mechanism has been studied extensively using solution kinetics.</p>

<p>2,5-Dihydroxybenzaldehyde is a compound that can be used as an antioxidant. It is also a precursor for the synthesis of benzalkonium chloride. 2,5-Dihydroxybenzaldehyde reacts with p-hydroxybenzoic acid to form 2,5-dihydroxyphenylacetic acid and benzoic acid. The reaction mechanism of 2,5-dihydroxybenzaldehyde has been studied in detail using hl-60 cells and has been shown to be significant cytotoxicity. The hydroxyl group in this molecule creates a hydrogen bond with the carbonyl group in p-hydroxybenzoic acid and the two react together to form products. This reaction is catalyzed by Michaelis–Menten kinetics and proceeds via an electrochemical detector. Nitrogen atoms are not present in this molecule but do exist in benzalkonium chloride, which is synthesized from 2</p>

3-(Methylthio)benzaldehyde is a molecule that can be used in the preparation of mandelic acid. It has been shown to inhibit the activity of lipase, an enzyme that breaks down fats. The cavity of 3-(methylthio)benzaldehyde has been studied by X-ray analysis and was found to have cationic character with silver ions. It also has functional groups that can be used for protein modification by enzymatic reactions.

<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>2,4,5-Trimethylbenzaldehyde is a cell line that can be used to study the oxidation of α-pinene. It is a chemical compound that belongs to the group of aromatic compounds and has been shown to have high cytotoxicity. It has been found to oxidize other molecules in the body with an electron acceptor such as oxygen or another molecule. 2,4,5-Trimethylbenzaldehyde has also been shown to have biological properties. This product is being researched for its ability to inhibit fatty acid synthesis and reduce cholesterol production in the liver.</p>

<p>3,5-Dibromosalicylaldehyde is a copper complex that has been synthesized from 3,5-dibromosalicylaldehyde and copper chloride. FTIR spectroscopy revealed that the coordination geometry of the copper complex is octahedral with two nitrogen atoms in the equatorial plane. The presence of hydrogen bonding interactions was confirmed by homologous protein adsorption experiments. This chemical structure was determined using X-ray crystallography and fluorescence probe experiments. The copper complex showed high affinity for malonic acid, which is an ester hydrochloride. The molecular mechanism of this interaction is based on adsorption, which occurs through hydrogen bonding interactions and hydrophobic interactions. Structural analysis revealed that the polymeric matrix consists of a three-dimensional network of crosslinked chains, while FTIR analysis indicated a possible disulfide bond between two cysteine residues.</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>3,5-Dinitrosalicylaldehyde is an oxidizing agent that is used in organic chemistry to produce aldehydes or carboxylic acids. It reacts with the amino groups of lysine residues and converts them to nitro groups. 3,5-Dinitrosalicylaldehyde is also used as a reagent in the determination of the number of lysine residues in proteins by titration with hydrochloric acid. The reaction mechanism of 3,5-dinitrosalicylaldehyde involves formation of an electron deficient intermediate that oxidizes chloride ions to form water molecules and chloride radicals. These intermediates react with nitro groups on lysine residues, resulting in nitro compounds. Crystallography studies have shown that the molecular structure of 3,5-dinitrosalicylaldehyde has two nitro groups and one hydroxyl group.</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>2,4-Dichloro-6-hydroxybenzaldehyde is a potential antineoplastic agent that inhibits mitochondrial function and induces apoptosis. This drug blocks the mitochondrial membrane potential and inhibits ATP production by blocking the mitochondrial respiratory chain complexes I and III. 2,4-Dichloro-6-hydroxybenzaldehyde has been shown to inhibit tumor cell growth in culture and in animal models of cancer. It also selectively kills tumor cells with low levels of cisplatin resistance through concurrent inhibition of mitochondria and caspase activation.<br>2,4-Dichloro-6-hydroxybenzaldehyde binds to both the inner membrane of mitochondria and to the plasma membrane of cancer cells, thereby inhibiting their function.</p>

<p>5-(4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl)furan-2-carbaldehyde is a heterocyclic compound that has been used to study protein tyrosine kinase activity. This drug binds to the active site of the enzyme and inhibits its function by forming an irreversible covalent bond with the enzyme's reactive cysteine residue, which prevents the transfer of phosphate groups from ATP to the substrate (tyrosine).</p>

<p>Retinylaldehyde is a derivative of vitamin A that is important for visual health. It is an inhibitor of the chloride channel, which may be due to its ability to inhibit alcohol dehydrogenase and polymerase chain reaction (PCR). Retinylaldehyde has been shown to have a high affinity for nuclear DNA and can bind to guanine nucleotide-binding protein (G protein) in neural cells. This activity leads to chronic cough in mice. Retinylaldehyde also has been shown as having significant up-regulation in human monocytes when exposed to toll-like receptor ligands. The role of retinylaldehyde in the immune system is not fully understood, but it may play a role in modulating the response to bacterial infection by altering the production of cytokines such as interleukin-1β (IL-1β) and tumor necrosis factor alpha (TNFα).</p>

<p>2-Fluoro-3-methylbenzaldehyde is a chemical that can be used in the synthesis of other chemicals, such as pharmaceuticals. It is a versatile building block that can be used in the synthesis of complex compounds and scaffolds. The compound has been shown to react with amines to form ureas.</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-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>3-Bromo-4,5-dimethoxybenzaldehyde is a molecule that is acidic in nature. It inhibits phosphatases and has shown cytotoxic activity against cancer cells in vitro. This compound also has antibacterial properties and can be used to treat bacterial infections. 3-Bromo-4,5-dimethoxybenzaldehyde is also a synthetic compound that can be found in the bisbenzylisoquinoline alkaloids family. It has been shown to have anti-tumor activity as well as an interaction with aldehydes and chalcones, which may lead to anti-inflammatory effects.</p>

<p>3,4-Dibenzyloxybenzaldehyde is a chemical compound with the formula ClCH=C(O)CHO. This compound is an intermediate in the synthesis of the cancer drug daunorubicin. 3,4-Dibenzyloxybenzaldehyde has been shown to induce apoptosis in human ovary cells and has been detected in urine samples from patients undergoing chemotherapy for ovarian cancer. 3,4-Dibenzyloxybenzaldehyde also inhibits the production of flavonoids and has been shown to inhibit rat striatal membranes and rat atria.</p>

<p>3,4-Dihydroxy-5-nitrobenzaldehyde is a chemical substance that is used in an analytical method to measure the level of methoxy groups in chronic kidney disease. The methanol solvent and hydrochloric acid are used to dissolve the sample, which is then titrated with trifluoroacetic acid. The chloride ion reacts with the methylene group from the 3,4-dihydroxy-5-nitrobenzaldehyde molecule to form a new compound that can be detected by ultraviolet light at 254 nm. The active methylene group is quantified by measuring its absorbance at this wavelength and comparing it with a calibration curve using known concentrations of sodium salts. This test has been shown to be more sensitive than other chromatographic methods for detecting methoxy groups in chronic kidney disease.</p>

6-Methoxy-2-naphthaldehyde is a nonsteroidal antiinflammatory drug that belongs to the class of naphthalenes. It inhibits the formation of inflammatory prostaglandins, which are mediators of pain and inflammation. 6-Methoxy-2-naphthaldehyde has been shown to have cytotoxic effects on cancer cells and in vitro studies have shown that it can induce cell lysis. It has also been shown to be a potent fluorescence probe for use in biological applications. This compound binds to human serum proteins by hydrogen bonding interactions, which may affect its pharmacokinetic properties. In addition, this compound has been shown to inhibit the activity of detoxification enzymes such as CYP 2C9 and 2D6 at high concentrations, which may lead to unwanted side effects such as nausea or vomiting. The molecular docking analysis of 6-Methoxy-2-naphthaldehyde with the active site of human liver alcohol dehydrogen

<p>2,4,6-Trihydroxybenzaldehyde is a polymerase chain inhibitor that blocks the synthesis of DNA and RNA. It has been shown to have significant cytotoxicity in vitro and has been used as an antimicrobial agent to inhibit the growth of bacteria. 2,4,6-Trihydroxybenzaldehyde also inhibits tetracycline resistance in Mycobacterium tuberculosis (Mtb) by inhibiting the production of proteins vital for bacterial cell division. This compound is structurally related to naturally occurring compounds such as anthocyanins and it has been shown to have inhibitory properties on mitochondrial membrane potential, which may be due to its ability to inhibit protein synthesis and induce apoptosis. The analytical methods used for this compound are thin layer chromatography and high performance liquid chromatography.</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.

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>3-Bromo-4-methoxybenzaldehyde is a heterocycle that contains a covalent inhibitor. It has been shown to have inhibitory activity against imines, hydroxyl groups, and human serum. 3-Bromo-4-methoxybenzaldehyde has been shown to be an efficient method for the synthesis of nitrogen containing heterocycles with potential use as pharmaceuticals. This compound has also been used in the asymmetric synthesis of diphenyl ethers, which are useful in pharmacological studies. The reaction mechanism of this compound is not well understood and needs more research before it can be applied to other areas.</p>

3-Carboxybenzaldehyde is a hydroxy aromatic compound with a molecular formula of C8H6O2. It is a synthetic chemical that can be used as an intermediate in the synthesis of other compounds, such as polycarboxylic acids. 3-Carboxybenzaldehyde has been shown to be an effective substrate for binding to polycarboxylic acid enzymes and activating them. This reaction generates the corresponding carboxylate product and releases CO2. 3-Carboxybenzaldehyde has also been used as a reactant in asymmetric synthesis reactions and shown to have some structural similarities with benzene ring structures.

<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>

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<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>2-Oxocyclohexanecarbaldehyde is a bifunctional carbonyl compound that reacts with amines to form carbinols. It can be used as a cheaper and more environmentally friendly alternative to the use of piperidine. 2-Oxocyclohexanecarbaldehyde also reacts with potassium hydride to form the corresponding ketones. The reaction of 2-oxocyclohexanecarbaldehyde with primary amines leads to isomeric products, depending on the position of substitution on the aromatic ring. This compound has been shown to react electrochemically in an asymmetric synthesis and has been used in the synthesis of morpholine, which is an important intermediate for pharmaceuticals, agrochemicals, and other chemical compounds.</p>

<p>3,4-Dimethoxy-5-hydroxybenzaldehyde is a phenolic compound that has been shown to be bactericidal against Listeria monocytogenes and Staphylococcus aureus. It has also been shown to have antioxidant properties in vivo. 3,4-Dimethoxy-5-hydroxybenzaldehyde may be used in the treatment of cardiovascular diseases such as atherosclerosis because it inhibits platelet aggregation and lipoprotein oxidation. The compound prevents the oxidation of prosthetic groups and the formation of adducts with DNA, which can lead to carcinogenesis. 3,4-Dimethoxy-5-hydroxybenzaldehyde is known to inhibit the growth of Pseudomonas aeruginosa, Salmonella typhimurium, Escherichia coli and Lactobacillus plantarum.</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-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>3,5-Dimethoxybenzaldehyde is a fungicide that can kill fungal cells by inhibiting the synthesis of ergosterol, an important component of the fungal cell membrane. It has been shown to be effective against Cryptococcus neoformans and other fungi. 3,5-Dimethoxybenzaldehyde inhibits mitochondrial superoxide production and the growth of fungi in a model system. The optimum concentration for inhibition was determined in a kinetic and thermodynamic study. This compound has also been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>4-Fluoro-3-phenoxybenzaldehyde is a chiral organic compound that has been synthesized in the laboratory. This compound has a linear response to peroxide and can be used as an environmental pollutant indicator. It is produced by the reaction of phenol with peroxide in deionized water, which is catalyzed by acid. The reaction time is dependent on the diluent used, and ultrasonic irradiation can be used to speed up the reaction. 4-Fluoro-3-phenoxybenzaldehyde's structure consists of two isomers, each containing either a fluorine atom or hydrogen atom on one of the phenyl rings. 4-Fluoro-3-phenoxybenzaldehyde can be purified using distillation or recrystallization techniques.</p>

<p>Gallaldehyde is a bioactive phenolic compound with antiproliferation activity. It has been shown to inhibit the growth of bacteria in vitro and also has hypoglycemic effects in mice. Gallaldehyde inhibits tyrosine kinase activity, which is needed for the growth of cells. Gallaldehyde is a tannin that can bind to proteins, inhibiting their functions. Gallaldehyde may also have anti-inflammatory properties due to its ability to inhibit the production of TNF-α induced by epidermal growth factor. This active form is metabolized by a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</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.

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<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>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>