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CAS 63216-49-9

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(1R,2S)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid

Description:
(1R,2S)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid is an amino acid derivative characterized by its cyclohexane ring structure, which contributes to its unique stereochemistry and physical properties. The presence of the tert-butoxycarbonyl (Boc) group provides protection for the amino group, making it useful in peptide synthesis and other organic reactions. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents, reflecting its functional groups. The carboxylic acid moiety imparts acidic characteristics, allowing it to participate in various chemical reactions, including esterification and amidation. Its stereochemistry, indicated by the (1R,2S) configuration, plays a crucial role in determining its biological activity and interactions with other molecules. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis, serving as a building block for more complex structures.
Formula:C12H21NO4
InChI:InChI=1/C12H21NO4/c1-12(2,3)17-11(16)13-9-7-5-4-6-8(9)10(14)15/h8-9H,4-7H2,1-3H3,(H,13,16)(H,14,15)/t8-,9+/m1/s1
Synonyms:
  • cyclohexanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (1R,2S)-
  • BOC-1,2-CIS-ACHC-OH
  • (1R,2S)-2-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic acid
  • (1R,2S)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylate
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