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CAS 517905-84-9

:

Fmoc-D-3-Amino-3-(2-bromophenyl)-propionic acid

Description:
Fmoc-D-3-Amino-3-(2-bromophenyl)-propionic acid is a synthetic amino acid derivative commonly used in peptide synthesis and drug development. It features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The compound contains a D-amino acid configuration, which can influence the biological activity and stability of peptides. The presence of a bromophenyl group enhances its hydrophobic character and can facilitate interactions with biological targets. This compound is typically characterized by its molecular structure, which includes an amino group, a carboxylic acid group, and a brominated aromatic ring. Its solubility is generally moderate in organic solvents, and it may exhibit specific reactivity patterns due to the bromine substituent. Overall, Fmoc-D-3-Amino-3-(2-bromophenyl)-propionic acid is valuable in the field of medicinal chemistry and peptide research for its unique structural features and functional properties.
Formula:C24H20BrNO4
InChI:InChI=1/C24H20BrNO4/c25-21-12-6-5-11-19(21)22(13-23(27)28)26-24(29)30-14-20-17-9-3-1-7-15(17)16-8-2-4-10-18(16)20/h1-12,20,22H,13-14H2,(H,26,29)(H,27,28)/t22-/m1/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@H](CC(=O)O)c1ccccc1Br)O
Synonyms:
  • (3R)-3-(2-Bromophenyl)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
  • benzenepropanoic acid, 2-bromo-beta-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (betaR)-
  • Fmoc-(R)-3-Amino-3-(2-bromophenyl)-propionic acid
  • Fmoc-(R)-3-Amino-3-(2-Bromo-Phenyl)-Propionic Acid
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