Building Blocks

<p>5-Ethenyl-2-methoxyphenol is a volatile compound that has been isolated from the bark of the cinnamon tree. It has shown anticancer activities "in vitro" and "in vivo". 5-Ethenyl-2-methoxyphenol has been shown to be demethylated by cytochrome P450 enzymes, which may result in its antitumor activity. This active compound can also be detected in postharvested fruit and vegetables as well as processed foods such as apple juice, tomato sauce, and dried fruits. 5-Ethenyl-2-methoxyphenol is responsible for the characteristic flavor of cinnamon, so it is often used as a flavoring agent in food processing.</p>

<p>2-Phenylbutan-1-amine is an optical isomer of the more common 1-phenylbutan-2-amine. It has been used as a chiral building block in the synthesis of pharmaceuticals and industrial products. 2-Phenylbutan-1-amine selectively reacts with propionic acid to produce optically pure 2-(4-methoxyphenyl)propionic acid, which can be used in the production of fluoroquinolone antibiotics, such as flurbiprofen. 2-Phenylbutan-1-amine has also been studied for its ability to hydrolyze microorganisms and amides.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 4-[8-[(2,6-Diethoxy-4′-fluoro[1,1′-biphenyl]-4-yl)methyl]-3-oxo-2,8-diazaspiro[4.5]dec-2-yl]benzoic acid hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2-Dihydropyrrolo[3,4-b]pyrrole-2,5-dione is a fine chemical that is used as a research chemical and in the synthesis of complex organic compounds. It is also an intermediate for the production of other chemicals. This compound can be used as a building block for the synthesis of many other chemicals with pharmaceutical and industrial applications. 1,2-Dihydropyrrolo[3,4-b]pyrrole-2,5-dione has been shown to be a useful reagent that can react with various functional groups to form new compounds and has found use in many industries.</p>

<p>2-Methyl-1-benzofuran-3-carboxylic acid is a type of carboxylic acid that is cytotoxic to cancer cells. It is a major metabolite of the anticancer drug 2,4,5-trimethoxybenzaldehyde and has been shown to be effective against human breast cancer cells. The ester hydrochloride salt form of this compound has been shown to be an effective inhibitor of esterase activity in vitro. This inhibition leads to increased accumulation of 2-methyl-1-benzofuran-3-carboxylic acid in tumor tissue, which may be due to its ability to inhibit the synthesis of proteins required for the transport and metabolism of other drugs. The x-ray structure analysis revealed that this compound binds to the active site of beta lactamases in an orientation that overlaps with substrate binding sites. This binding prevents the formation of a covalent bond between penicillin G</p>

<p>1,2-Dioleoyl-sn-glycerol is a lipid molecule that contains an acyl chain of carbon atoms with two double bonds. It is formed through the union of glycerol and oleic acid. 1,2-Dioleoyl-sn-glycerol has been shown to activate diacylglycerol and fatty acid, which are important for cell signaling. The enzyme activity of 1,2-dioleoyl-sn-glycerol is dependent on its concentration in the body. This molecule also interacts with membranes by hydrogen bonding and can form a hydrophobic region that may be used to stabilize membrane structures.</p>

<p>3,5-Diamino-N-carbamothioyl-6-chloropyrazine-2-carboxamide is a high quality, useful intermediate and reagent for the production of fine chemicals. It is also a speciality chemical that has been used as a reaction component in research. 3,5-Diamino-N-carbamothioyl-6-chloropyrazine-2-carboxamide is an important versatile building block that can be used to produce many other compounds.</p>

<p>2,6-Dichloro-3,5-dihydroxybenzoic acid is a reagent with a wide range of applications in the research and development of chemical products. It is also a useful intermediate for the synthesis of other compounds. 2,6-Dichloro-3,5-dihydroxybenzoic acid has been shown to be used as a building block for the synthesis of various complex compounds. It is also an important reaction component that can be used in many different reactions to produce valuable products.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-[3-(Trifluoromethyl)phenyl]-1H-1,2,3-triazole-4-carboxylic acid (TFTCA) is a versatile building block used as a reagent in research and speciality chemical synthesis. TFTCA is used as a reactant in the synthesis of complex compounds and can be used as an intermediate or scaffold. The compound has been used to synthesize drugs such as 3,5-dichloro-N-(3-(trifluoromethyl)phenyl)-2-thiophenecarboxamide (PF23410), which is a potent inhibitor of protein kinase C.</p>

<p>3,4-Difluoro-5-nitrobenzonitrile is a hepatotoxic compound that is found in the environment. It has been shown to cause cirrhosis and overgrowth of the liver. 3,4-Difluoro-5-nitrobenzonitrile also inhibits hepatic encephalopathy and may be used to treat liver disease. This toxicant has been detected in the bowel and duodenum of humans with nonalcoholic steatohepatitis, as well as in the jejunum and duodenum of mice with spontaneous steatohepatitis. It also causes nonalcoholic steatohepatitis when given orally to rats.</p>

<p>Versatile small molecule scaffold</p>

<p>3,4-Diaminobenzoic acid is a compound that is produced by the condensation of two molecules of hydrochloric acid. 3,4-Diaminobenzoic acid has been used as a reagent in the synthesis of coumarin derivatives. This chemical has been shown to be an effective proton scavenger in an optimum concentration. Benzimidazole compounds are also synthesized from 3,4-diaminobenzoic acid and have been shown to be effective against autoimmune diseases. 3,4-Diaminobenzoic acid can be used for the production of diazonium salts, which are used in the synthesis of anti-inflammatory drugs and other pharmaceuticals. The hydroxyl group on this molecule makes it chemically stable and kinetic data shows that it has high diphenolase activity.</p>

<p>2,3-Dichloropyridine is an organic compound with the formula P(Cl)Cl. It is a white crystalline solid that reacts violently with water and alcohols. 2,3-Dichloropyridine can be used for the preparation of dichloroacetic acid by reaction with phosphorus pentachloride in the presence of sodium carbonate and water vapor. This compound can also be used to prepare copper chloride by reaction with diazonium salt in hydrochloric acid and chlorine atom in the presence of sodium carbonate at low energy.</p>

<p>4,5-Dichloro-1,2-phenylenediamine is a cytotoxic agent that can inhibit the enzymes urea amidolyase and fatty acid synthase in tissue culture. This compound also inhibits the production of urea nitrogen and fatty acids in human serum. 4,5-Dichloro-1,2-phenylenediamine may be useful as a cancer treatment because it has been shown to cause leukemia cell death as well as inhibition of t-cell proliferation. The drug may also induce apoptosis by inhibiting DNA synthesis through its reaction with benzimidazole compounds. The basic structure of 4,5-Dichloro-1,2-phenylenediamine is similar to protocatechuic acid and malignant brain tumor cells.</p>

<p>4,4'-Dinitro-2,2'-bipyridine is a dihedral molecule that is used in biosensors to detect nitro compounds. It is synthesized by the reaction of osmium tetroxide with pyridine. The transfer of electrons from the pyridine ring to the osmium atom results in an oriented molecule with a positive charge on one end and a negative charge on the other end. This orientation can be reversed by oxidation. 4,4'-Dinitro-2,2'-bipyridine has been shown to react with monoalcohols and nucleophiles such as water to form covalent bonds. It also reacts with radiation, which may account for its use in dosimeters for measuring radiation exposure.</p>

<p>2,5-Dihydroxybenzoic acid is a natural compound that has been shown to inhibit the matrix metalloproteinase enzyme activity of α1-acid glycoprotein. The 2,5-dihydroxybenzoic acid structure is similar to p-hydroxybenzoic acid and gentisic acid. It is also an inhibitor of xanthine oxidase and caffeic acid oxidase. 2,5-Dihydroxybenzoic acid has a number of potential uses in analytical chemistry as it can be used to measure the concentrations of caffeic acids and other related compounds in biological samples.</p>

<p>2-(Nitromethylidene)-1,3-thiazinane is a chemical compound that has been shown to have chronic toxic effects in animal studies. It binds to the ryanodine receptor and inhibits the release of calcium from the sarcoplasmic reticulum, which may lead to an increase in acetylcholine, a neurotransmitter involved in many aspects of brain function. 2-(Nitromethylidene)-1,3-thiazinane has also been shown to inhibit the activity of neonicotinoids, insecticides that are used for agricultural and veterinary purposes. This compound is structurally similar to other non-competitive inhibitors of acetylcholine esterase, such as piperonyl butoxide.</p>