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CAS 220497-64-3

:

(1S,4R)-N-FMOC-1-Aminocyclopent-2-ene-4-carboxylic acid

Description:
(1S,4R)-N-FMOC-1-Aminocyclopent-2-ene-4-carboxylic acid is a chemical compound characterized by its unique bicyclic structure, which includes a cyclopentene ring. The "N-FMOC" designation indicates that it is protected with a 9-fluorenylmethoxycarbonyl (FMOC) group, commonly used in peptide synthesis to protect amine functionalities. This compound features both an amino group and a carboxylic acid group, making it an amino acid derivative. The stereochemistry is specified by the (1S,4R) notation, indicating the specific spatial arrangement of atoms around the chiral centers, which is crucial for its biological activity and interactions. The presence of the cyclopentene moiety contributes to its rigidity and potential reactivity in various chemical reactions. This compound is often utilized in organic synthesis and peptide chemistry, particularly in the development of novel peptides and pharmaceuticals. Its unique structure and functional groups make it a valuable intermediate in the synthesis of more complex molecules.
Formula:C21H19NO4
InChI:InChI=1/C21H19NO4/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/h1-10,13-14,19H,11-12H2,(H,22,25)(H,23,24)/t13-,14+/m1/s1
Synonyms:
  • (1S,4R)-N-(9-Fluorenylmethoxycarbonyl)-1-amino-2-cyclopentene-4-carboxylic acid
  • (-)-(1R,4S)-N-Fmoc-1-aminocyclopent-2-ene-4-carboxylic acid
  • (-)-(1S,4R)-N-Fmoc-4-Aminocyclopent-2-enecarboxylic acid
  • Fmoc-D-ACPEC
  • (1S,4R)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclopent-2-ene-1-carboxylic acid
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