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CAS 507472-14-2

:

(βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-fluorobenzenepropanoic acid

Description:
The chemical substance known as (βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-fluorobenzenepropanoic acid, with the CAS number 507472-14-2, is a synthetic compound primarily used in the field of medicinal chemistry and peptide synthesis. It features a fluorinated aromatic ring, which can enhance its biological activity and lipophilicity. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates that it is likely used as a protecting group for amino acids during peptide synthesis, allowing for selective reactions without interfering with the amine functionality. The compound's structure suggests it has both hydrophilic and hydrophobic characteristics, which may influence its solubility and interaction with biological membranes. Additionally, the presence of a carboxylic acid functional group indicates potential for forming salts or participating in acid-base reactions. Overall, this compound is of interest for its potential applications in drug development and as a building block in the synthesis of more complex molecules.
Formula:C24H20FNO4
InChI:InChI=1S/C24H20FNO4/c25-16-7-5-6-15(12-16)22(13-23(27)28)26-24(29)30-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1
InChI key:InChIKey=ZZERQNLGPZUNLM-QFIPXVFZSA-N
SMILES:C(OC(N[C@@H](CC(O)=O)C1=CC(F)=CC=C1)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (3S)-3-([[(9H-Fluoren-9-yl)methoxy]carbonyl]amino)-3-(3-fluorophenyl)propanoic acid
  • (βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-fluorobenzenepropanoic acid
  • Benzenepropanoic acid, β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-3-fluoro-, (βS)-
  • Fmoc-(S)-3-Amino-3-(3-Fluoro-Phenyl)-Propionic Acid
  • Fmoc-(S)-3-Amino-3-(3-fluorophenyl)-propionic acid
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