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CAS 130981-12-3

:

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

Description:
(1R,2S)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylic acid is a chiral compound characterized by its cyclopentane ring structure, which features a carboxylic acid functional group and a tert-butoxycarbonyl (Boc) protecting group on the amino group. The presence of the Boc group indicates that this compound is likely used in peptide synthesis or as an intermediate in organic synthesis, as it provides a means to protect the amino functionality during reactions. The specific stereochemistry, denoted by the (1R,2S) configuration, suggests that the compound exhibits optical activity, which can influence its biological activity and interactions. This compound is typically solid at room temperature and is soluble in polar organic solvents. Its properties, such as melting point, boiling point, and reactivity, would be influenced by the steric and electronic effects of the substituents on the cyclopentane ring. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry due to its structural features and potential applications.
Formula:C11H19NO4
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7(8)9(13)14/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/t7-,8+/m1/s1
Synonyms:
  • cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (1R,2S)-
  • (1R,2S)-2-[(tert-Butoxycarbonyl)amino]cyclopentanecarboxylic acid
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