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CAS 134003-04-6

:

(1R,4S)-4-Aminocyclopent-2-ene-1-carboxylic acid

Description:
(1R,4S)-4-Aminocyclopent-2-ene-1-carboxylic acid, with the CAS number 134003-04-6, is an organic compound characterized by its cyclopentene structure, which features a carboxylic acid functional group and an amino group. This compound exhibits chirality, with specific stereochemistry at the 1 and 4 positions, contributing to its potential biological activity. The presence of the amino group suggests that it may participate in various biochemical processes, possibly acting as an amino acid or a precursor to other biologically relevant molecules. The cyclopentene ring provides a degree of rigidity, influencing its reactivity and interactions with other molecules. Additionally, the carboxylic acid group imparts acidic properties, allowing for proton donation in solution, which can affect solubility and reactivity. Overall, this compound may have applications in medicinal chemistry and biochemistry, particularly in the design of pharmaceuticals or as a building block in organic synthesis. Its specific stereochemistry and functional groups make it a subject of interest for further research in these fields.
Formula:C6H9NO2
InChI:InChI=1S/C6H9NO2/c7-5-2-1-4(3-5)6(8)9/h1-2,4-5H,3,7H2,(H,8,9)/t4-,5+/m0/s1
InChI key:InChIKey=VTCHZFWYUPZZKL-CRCLSJGQSA-N
SMILES:C(O)(=O)[C@@H]1C[C@H](N)C=C1
Synonyms:
  • (+)-(1S,4R)-1-amino-cyclopent-2-ene-4-carboxylic acid
  • (1R,4S)-4-Amino-2-cyclopentene-1-carboxylic acid
  • (1R,4S)-4-aminocyclopent-2-ene-1-carboxylic acid
  • 2-Cyclopentene-1-carboxylic acid, 4-amino-, (1R,4S)-
  • 2-Cyclopentene-1-carboxylic acid, 4-amino-, (1R-cis)-
  • L-AcPEC
  • (1R,4S)-4-Aminocyclopent-2-enecarboxylic acid
  • (+)-(1R,4S)-4-Aminocyclopent-2-enecarboxylic acid
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