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CAS 132487-40-2

:

(1S,2R)-(-)-2-Aminocyclohex-3-enecarboxylic acid hydrochloride

Description:
(1S,2R)-(-)-2-Aminocyclohex-3-enecarboxylic acid hydrochloride, with the CAS number 132487-40-2, is a chiral amino acid derivative characterized by its cyclohexene structure. This compound features a carboxylic acid functional group and an amino group, which contribute to its properties as an amino acid. The specific stereochemistry indicated by the (1S,2R) configuration suggests that it has distinct spatial arrangements, influencing its biological activity and interactions. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in various applications, including pharmaceuticals and biochemical research. The presence of the cyclohexene ring introduces rigidity to the molecule, which can affect its reactivity and binding properties. This compound may be of interest in studies related to neurotransmitter systems or as a building block in the synthesis of more complex molecules. Overall, its unique structural features and stereochemistry make it a valuable compound in both research and potential therapeutic contexts.
Formula:C7H12ClNO2
InChI:InChI=1/C7H11NO2.ClH/c8-6-4-2-1-3-5(6)7(9)10;/h2,4-6H,1,3,8H2,(H,9,10);1H/t5-,6+;/m0./s1
Synonyms:
  • (1S,2R)-2-ammoniocyclohex-3-ene-1-carboxylate
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