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CAS 865430-78-0

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3,5-Pyridinedicarboxylic acid, 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, hydrobromide (1:1), (4S)-

Description:
3,5-Pyridinedicarboxylic acid, 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, hydrobromide (1:1), (4S)-, is a complex organic compound characterized by its pyridine ring structure, which is substituted at multiple positions. The presence of two carboxylic acid groups indicates its potential as a dicarboxylic acid derivative, while the hydrobromide salt form suggests enhanced solubility in polar solvents. The compound features an aminoethoxy side chain, which may contribute to its biological activity or interaction with biological systems. The chlorophenyl group adds to its structural diversity and may influence its pharmacological properties. Additionally, the stereochemistry indicated by (4S)- suggests specific spatial arrangements that could affect its reactivity and interactions. Overall, this compound's unique combination of functional groups and stereochemistry may render it of interest in medicinal chemistry or as a potential pharmaceutical agent. Further studies would be necessary to elucidate its specific properties and applications.
Formula:C20H25ClN2O5·BrH
InChI:InChI=1S/C20H25ClN2O5.BrH/c1-4-28-20(25)18-15(11-27-10-9-22)23-12(2)16(19(24)26-3)17(18)13-7-5-6-8-14(13)21;/h5-8,17,23H,4,9-11,22H2,1-3H3;1H/t17-;/m0./s1
InChI key:InChIKey=RVCDRXDQZIUQJA-LMOVPXPDSA-N
SMILES:C(OCC)(=O)C=1[C@H](C(C(OC)=O)=C(C)NC1COCCN)C2=C(Cl)C=CC=C2.Br
Synonyms:
  • (S)-Amlodipine hydrobromide
  • (S)-(-)-Amlodipine hydrobromide
  • 3,5-Pyridinedicarboxylic acid, 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, hydrobromide (1:1), (4S)-
  • 3,5-Pyridinedicarboxylic acid, 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, monohydrobromide, (4S)-
  • Levamlodipine hydrobromide
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