CAS 79925-38-5
:3,5-Pyridinedicarboxylic acid,4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, diethyl ester
Description:
3,5-Pyridinedicarboxylic acid, 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, diethyl ester, with CAS number 79925-38-5, is a chemical compound that belongs to the class of pyridine derivatives. This compound features a pyridine ring substituted with two carboxylic acid groups and an ester functional group, which contributes to its reactivity and solubility characteristics. The presence of the dichlorophenyl group enhances its biological activity and potential applications in pharmaceuticals or agrochemicals. The diethyl ester moiety suggests that the compound may exhibit moderate lipophilicity, influencing its absorption and distribution in biological systems. Additionally, the presence of multiple functional groups indicates potential for various chemical reactions, including hydrolysis and esterification. Overall, this compound's unique structure may confer specific properties that could be explored for various applications in medicinal chemistry or material science. However, detailed studies would be necessary to fully understand its behavior and potential uses.
Formula:C19H21Cl2NO4
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Found 5 products.
Felodipine EP Impurity C
CAS:Formula:C19H21Cl2NO4Color and Shape:White To Off-White SolidMolecular weight:398.28Diethyl 4-(2,3-Dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
CAS:Controlled ProductFormula:C19H21Cl2NO4Color and Shape:NeatMolecular weight:398.28Nemadipine B
CAS:Controlled ProductImpurity Felodipine EP Impurity C
Applications Nemadipine B (Felodipine EP Impurity C) is the diethyl ester analogue analogue of the calcium channel blocker Felodipine (F232375) with antihypertensive activity.
References Berntsson, P. et al.: J. Cardio. Pharmacol., 10, S60 (1987); Kwok, T.C. et al.: Nature, 441, 91 (2008);Formula:C19H21Cl2NO4Color and Shape:NeatMolecular weight:398.28Nemadipine B
CAS:Nemadipine B is a synthetic drug that has been shown to have an antioxidant effect. It binds to the hydrophobic pocket of the cytochrome P450 enzyme, causing activation of this protein. Nemadipine B also inhibits chloride channels and prevents the formation of acid, which is necessary for the degradation of lipids. This drug has been shown to have a hemolytic activity in vitro and in vivo. The reaction products of nemadipine B consist mainly of phenylacetic acid, acetophenone, and 2-hydroxy-5-(2-methylpropyl)benzaldehyde with small amounts of carbon dioxide and water. Nemadipine B is a blocker for l-type calcium channels that can be used for treatment of cardiac arrhythmia.Formula:C19H21Cl2NO4Purity:Min. 95%Molecular weight:398.28 g/mol




