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CAS 140171-66-0

:

3,5-Dimethyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate

Description:
3,5-Dimethyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate is a complex organic compound characterized by its multi-functional structure, which includes a pyridine ring and various substituents that contribute to its chemical properties. The presence of two methyl groups on the pyridine ring enhances its lipophilicity, potentially affecting its solubility and biological activity. The aminoethoxy group suggests potential for hydrogen bonding and interaction with biological targets, which may be relevant in pharmacological contexts. The chlorophenyl substituent can influence the compound's electronic properties and reactivity. As a dihydropyridine derivative, it may exhibit properties typical of this class, such as calcium channel blocking activity, which is significant in medicinal chemistry. The compound's molecular structure indicates potential applications in drug development, particularly in areas related to cardiovascular health or neuropharmacology. However, specific biological activity, toxicity, and stability would require further investigation through empirical studies.
Formula:C19H23ClN2O5
InChI:InChI=1S/C19H23ClN2O5/c1-11-15(18(23)25-2)16(12-6-4-5-7-13(12)20)17(19(24)26-3)14(22-11)10-27-9-8-21/h4-7,16,22H,8-10,21H2,1-3H3
InChI key:InChIKey=UDSAEMGNQXMCDF-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1C(C(C(OC)=O)=C(C)NC1COCCN)C2=C(Cl)C=CC=C2
Synonyms:
  • 2-[(2-Aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylic acid dimethyl ester
  • 3,5-Dimethyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate
  • 3,5-Pyridinedicarboxylic acid, 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3,5-dimethyl ester
  • 3,5-Pyridinedicarboxylic acid, 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, dimethyl ester
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