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CAS 403661-79-0

:

(βS)-2-Bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid

Description:
(βS)-2-Bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid is a chemical compound characterized by its complex structure, which includes a bromine atom, a fluorenylmethoxycarbonyl (Fmoc) protecting group, and a benzenebutanoic acid moiety. This compound is typically used in peptide synthesis and other organic chemistry applications due to its ability to protect amino groups during reactions. The presence of the bromine atom introduces a site for potential nucleophilic substitution reactions, enhancing its reactivity. The Fmoc group is particularly valuable in solid-phase peptide synthesis, allowing for selective deprotection under mild conditions. The stereochemistry indicated by the (βS) designation suggests specific spatial arrangements of atoms, which can influence the compound's biological activity and interactions. Overall, this compound is significant in the field of medicinal chemistry and peptide research, providing a versatile building block for the synthesis of more complex molecules.
Formula:C25H22BrNO4
InChI:InChI=1S/C25H22BrNO4/c26-23-12-6-1-7-16(23)13-17(14-24(28)29)27-25(30)31-15-22-20-10-4-2-8-18(20)19-9-3-5-11-21(19)22/h1-12,17,22H,13-15H2,(H,27,30)(H,28,29)/t17-/m0/s1
InChI key:InChIKey=WLVUAXHMNMNOKU-KRWDZBQOSA-N
SMILES:C(OC(N[C@@H](CC1=C(Br)C=CC=C1)CC(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (S)-N-(9-Fluorenylmethoxycarbonyl)-3-Amino-4-(2-Bromo-Phenyl)-Butyric Acid
  • (βS)-2-Bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid
  • Fmoc-(S)-3-Amino-4-(2-Bromo-Phenyl)-Butyric Acid
  • Fmoc-(S)-3-Amino-4-(2-Bromophenyl)Butanoic Acid
  • Fmoc-2-Bromo-L-Beta-Homophenylalanine
  • Fmoc-Beta-Hophe(2-Br)-Oh
  • Fmoc-Phe(2-Br)-(C*Ch2)Oh
  • N-Beta-(9-Fluorenylmethoxycarbonyl)-Beta-L-Homo(2-Bromophenyl)Alanine
  • Rarechem Ak Pt F131
  • Benzenebutanoic acid, 2-bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βS)-
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