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CAS 26685-83-6

:

(1R,2R)-2-Aminocyclohexanecarboxylic acid

Description:
(1R,2R)-2-Aminocyclohexanecarboxylic acid, commonly known as L-2-Aminocyclohexanecarboxylic acid, is an amino acid derivative characterized by its cyclohexane ring structure with an amino group and a carboxylic acid functional group. This compound is a chiral molecule, meaning it exists in two enantiomeric forms, with the (1R,2R) configuration being biologically relevant. It is typically a white crystalline solid that is soluble in water due to the presence of the polar carboxylic acid and amino groups. This compound is of interest in various fields, including medicinal chemistry and biochemistry, as it can serve as a building block for the synthesis of peptides and other biologically active molecules. Its structural features contribute to its potential role in influencing biological activity, particularly in the context of neurotransmitter function and receptor interactions. Additionally, its stereochemistry can significantly affect its pharmacological properties, making it a subject of study in drug design and development.
Formula:C7H13NO2
InChI:InChI=1/C7H13NO2/c8-6-4-2-1-3-5(6)7(9)10/h5-6H,1-4,8H2,(H,9,10)/t5-,6-/m1/s1
InChI key:InChIKey=USQHEVWOPJDAAX-PHDIDXHHSA-N
SMILES:C(O)(=O)[C@H]1[C@H](N)CCCC1
Synonyms:
  • Cyclohexanecarboxylic acid, 2-amino-, (1R-trans)-
  • cyclohexanecarboxylic acid, 2-amino-, (1R,2R)-
  • trans-(1R,2R)-2-Aminocyclohexane-1-carboxylic acid
  • trans-(1R,2R)-2-Aminocyclohexanecarboxylic acid
  • (1R,2R)-2-Aminocyclohexanecarboxylic acid
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