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CAS 488703-61-3

:

(1S,2S)-2-(Aminocarbonyl)cyclohexanecarboxylic acid

Description:
(1S,2S)-2-(Aminocarbonyl)cyclohexanecarboxylic acid, with the CAS number 488703-61-3, is a chiral compound characterized by its cyclohexane ring structure, which features a carboxylic acid group and an aminocarbonyl substituent. This compound exhibits both acidic and basic properties due to the presence of the carboxylic acid and the amine functional groups, respectively. Its chirality is significant in biological systems, as it may influence the compound's interaction with enzymes and receptors. The presence of the aminocarbonyl group suggests potential applications in medicinal chemistry, particularly in the design of pharmaceuticals that target specific biological pathways. Additionally, the compound's solid-state properties, such as melting point and solubility, can vary based on its stereochemistry and the presence of functional groups, which may affect its stability and reactivity. Overall, (1S,2S)-2-(Aminocarbonyl)cyclohexanecarboxylic acid is of interest for its potential applications in drug development and its role in organic synthesis.
Formula:C8H13NO3
InChI:InChI=1S/C8H13NO3/c9-7(10)5-3-1-2-4-6(5)8(11)12/h5-6H,1-4H2,(H2,9,10)(H,11,12)/t5-,6-/m0/s1
InChI key:InChIKey=LNNRRNLGMOUZCT-WDSKDSINSA-N
SMILES:C(N)(=O)[C@@H]1[C@@H](C(O)=O)CCCC1
Synonyms:
  • (1S,2S)-2-(Aminocarbonyl)cyclohexanecarboxylic acid
  • Cyclohexanecarboxylic acid, 2-(aminocarbonyl)-, (1S,2S)-
  • 2-(5-phenyl-4H-1,2,4-triazol-3-yl)ethanamine
  • (S,S)-2-Carbamoylcyclohexanecarboxylic acid
  • (1S,2S)-3-carbamoylcyclohexanecarboxylic acid
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