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CAS 220497-67-6

:

(1R,3S)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclopentanecarboxylic acid

Description:
(1R,3S)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclopentanecarboxylic acid, with CAS number 220497-67-6, is a synthetic organic compound characterized by its unique structural features. It contains a cyclopentanecarboxylic acid moiety, which contributes to its potential as a building block in peptide synthesis and drug development. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates that this compound is likely used in solid-phase peptide synthesis as a protective group for amino acids, facilitating the assembly of peptides while preventing unwanted reactions. The specific stereochemistry, denoted by the (1R,3S) configuration, suggests that the compound exhibits chirality, which can influence its biological activity and interactions. Additionally, the compound's solubility and stability in various solvents can vary, impacting its application in laboratory settings. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis, owing to its functional groups and structural characteristics that enable diverse chemical reactivity and biological interactions.
Formula:C21H21NO4
InChI:InChI=1S/C21H21NO4/c23-20(24)13-9-10-14(11-13)22-21(25)26-12-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-8,13-14,19H,9-12H2,(H,22,25)(H,23,24)/t13-,14+/m1/s1
InChI key:InChIKey=BHDMUBZVWRSQOT-KGLIPLIRSA-N
SMILES:C(OC(N[C@@H]1C[C@H](C(O)=O)CC1)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (-)-(1R,3S)-N-Fmoc-3-Aminocyclopentanecarboxylic acid
  • (1R,3R)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclopentanecarboxylic acid
  • (1R,3S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclopentanecarboxylic acid
  • (1R,3S)-N-Fmoc-3-Aminocyclopentane-1-carboxylic acid
  • (1S,3R)-N-(9-Fluorenylmethoxycarbonyl)-1-aminocyclopentane-3-carboxylic acid
  • Cyclopentanecarboxylic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (1R,3S)-
  • Fmoc-D-ACPAC
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