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CAS 752181-59-2

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Cyclopentanecarboxylicacid, 2-amino-, ethyl ester, (1S,2S)-

Description:
Cyclopentanecarboxylic acid, 2-amino-, ethyl ester, (1S,2S)-, is a chiral compound characterized by its cyclopentane ring structure, which is substituted with a carboxylic acid and an amino group. The presence of the ethyl ester functional group indicates that it is an ester derivative, which typically enhances its solubility in organic solvents. The (1S,2S) designation refers to the specific stereochemistry of the molecule, indicating that it has two chiral centers, which can significantly influence its biological activity and reactivity. This compound may exhibit properties typical of amino acids and esters, such as potential interactions with biological systems, making it of interest in pharmaceutical and biochemical research. Its CAS number, 752181-59-2, allows for precise identification in chemical databases. Overall, the unique structural features and stereochemistry of this compound contribute to its potential applications in various fields, including medicinal chemistry and organic synthesis.
Formula:C8H15NO2
Synonyms:
  • Cyclopentanecarboxylicacid, 2-amino-, ethyl ester, (1S-trans)- (9CI)
  • Cyclopentanecarboxylic acid, 2-amino-, ethyl ester, (1S,2S)-
  • ethyl (1S,2S)-2-aminocyclopentane-1-carboxylate
  • Ethyl (1S,2S)-2-AMinocyclopentanecarboxylate
  • Ethyl (1S,2S)-2-Aminocyclopentanecarboxylate, ≥95%
  • (1S,2S)-Ethyl 2-aminocyclopentanecarboxylate
  • Cyclopentanecarboxylic acid, 2-amino-, ethyl ester, (1S-trans)- (9CI)
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