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CAS 71830-07-4

:

(1S,3R)-3-Aminocyclopentanecarboxylic acid

Description:
(1S,3R)-3-Aminocyclopentanecarboxylic acid, with the CAS number 71830-07-4, is a cyclic amino acid characterized by its unique structural features. It contains a cyclopentane ring with an amino group and a carboxylic acid functional group, which contribute to its properties as a chiral compound. The specific stereochemistry indicated by the (1S,3R) configuration suggests that it has distinct spatial arrangements, influencing its biological activity and interactions. This compound is typically soluble in polar solvents due to the presence of the carboxylic acid group, which can engage in hydrogen bonding. Its amino group can also participate in various chemical reactions, making it a potential candidate for applications in pharmaceuticals and biochemistry. The presence of both functional groups allows it to act as a building block in peptide synthesis or as a ligand in coordination chemistry. Overall, (1S,3R)-3-Aminocyclopentanecarboxylic acid is of interest in research fields exploring amino acid derivatives and their roles in biological systems.
Formula:C6H11NO2
InChI:InChI=1S/C6H11NO2/c7-5-2-1-4(3-5)6(8)9/h4-5H,1-3,7H2,(H,8,9)/t4-,5+/m0/s1
InChI key:InChIKey=MLLSSTJTARJLHK-CRCLSJGQSA-N
SMILES:C(O)(=O)[C@@H]1C[C@H](N)CC1
Synonyms:
  • (+)-(1R,3S)-1-amino-cyclopent-2-ene-4-carboxylic acid
  • (+)-cis-3-Aminocyclopentanecarboxylic acid
  • (1S,3R)-3-Aminocyclopentane-1-carboxylic acid
  • Cyclopentanecarboxylic acid, 3-amino-, (1S,3R)-
  • Cyclopentanecarboxylic acid, 3-amino-, (1S-cis)-
  • L-AcPAC
  • (+)-(1S,3R)-3-Aminocyclopentanecarboxylic acid
  • (1S,3R)-3-Aminocyclopentanecarboxylic acid
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