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CAS 76093-34-0

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(4S)-5-(methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid

Description:
The chemical substance known as (4S)-5-(methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid, with the CAS number 76093-34-0, is a member of the dihydropyridine class of compounds, which are characterized by a six-membered ring containing nitrogen. This compound features multiple functional groups, including a methoxycarbonyl group and a nitrophenyl substituent, which contribute to its chemical reactivity and potential biological activity. The presence of the carboxylic acid group indicates that it can participate in acid-base reactions and may exhibit solubility in polar solvents. The stereochemistry, denoted by the (4S) configuration, suggests specific spatial arrangements that can influence the compound's interactions with biological targets. Dihydropyridines are often studied for their pharmacological properties, particularly as calcium channel blockers, and this compound may exhibit similar properties due to its structural features. Overall, its unique combination of substituents and stereochemistry makes it a compound of interest in medicinal chemistry and related fields.
Formula:C16H16N2O6
InChI:InChI=1/C16H16N2O6/c1-8-12(15(19)20)14(13(9(2)17-8)16(21)24-3)10-5-4-6-11(7-10)18(22)23/h4-7,14,17H,1-3H3,(H,19,20)/t14-/m0/s1
SMILES:CC1=C([C@H](c2cccc(c2)N(=O)=O)C(=C(C)N1)C(=O)OC)C(=O)O
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