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CAS 71830-08-5

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

Description:
(1R,3S)-3-Aminocyclopentanecarboxylic acid, also known as a cyclic amino acid, is characterized by its unique structure that includes a cyclopentane ring with an amino group and a carboxylic acid functional group. This compound exhibits chirality, with specific stereochemistry at the 1 and 3 positions, which influences its biological activity and interactions. It is typically a white to off-white solid and is soluble in water due to the presence of the polar carboxylic acid and amino groups. The compound is of interest in medicinal chemistry and biochemistry, as it can serve as a building block for peptide synthesis or as a potential therapeutic agent. Its properties, such as melting point, boiling point, and reactivity, can vary based on environmental conditions and the presence of other functional groups. Additionally, its stereochemistry may affect its binding affinity to biological targets, making it a subject of study in drug design and development.
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+/m1/s1
InChI key:InChIKey=MLLSSTJTARJLHK-UHNVWZDZSA-N
SMILES:C(O)(=O)[C@H]1C[C@@H](N)CC1
Synonyms:
  • (-)-(1S,3R)-1-amino-cyclopent-2-ene-4-carboxylic acid
  • (-)-cis-3-Aminocyclopentanecarboxylic acid
  • Cyclopentanecarboxylic acid, 3-amino-, (1R,3S)-
  • Cyclopentanecarboxylic acid, 3-amino-, (1R-cis)-
  • D-Acpac
  • (-)-(1R,3S)-3-Aminocyclopentanecarboxylic acid
  • (1R,3S)-3-Aminocyclopentanecarboxylic acid
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