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CAS 454709-98-9

:

rel-1,1-Dimethylethyl N-[(1R,3S)-3-aminocyclopentyl]carbamate

Description:
Rel-1,1-Dimethylethyl N-[(1R,3S)-3-aminocyclopentyl]carbamate, with the CAS number 454709-98-9, is a chemical compound characterized by its unique structural features, including a carbamate functional group and a cyclopentyl moiety. This compound typically exhibits properties associated with amines and carbamates, such as potential solubility in polar solvents and the ability to form hydrogen bonds due to the presence of amino and carbamate groups. Its stereochemistry, indicated by the (1R,3S) configuration, suggests specific spatial arrangements that can influence its biological activity and interactions with other molecules. The presence of the dimethyl group contributes to steric hindrance, which may affect its reactivity and binding affinity in biological systems. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential role as a bioactive agent. As with many organic compounds, its stability, reactivity, and interactions would depend on environmental conditions such as pH and temperature.
Formula:C10H20N2O2
InChI:InChI=1/C10H20N2O2/c1-10(2,3)14-9(13)12-8-5-4-7(11)6-8/h7-8H,4-6,11H2,1-3H3,(H,12,13)/t7-,8+/s2
InChI key:InChIKey=PGBVMVTUWHCOHX-HGXVMFPFNA-N
SMILES:N(C(OC(C)(C)C)=O)[C@@H]1C[C@H](N)CC1
Synonyms:
  • tert-Butyl (cis-3-aminocyclopentyl)carbamate
  • Carbamic acid, [(1R,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester, rel-
  • Carbamic acid, N-[(1R,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester, rel-
  • cis-(3-Aminocyclopentyl)-carbamic acid tert-butyl ester
  • rel-1,1-Dimethylethyl N-[(1R,3S)-3-aminocyclopentyl]carbamate
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