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CAS 270062-85-6

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Boc-(S)-3-amino-4-(4-bromo-phenyl)-butyric acid

Description:
Boc-(S)-3-amino-4-(4-bromo-phenyl)-butyric acid is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (Boc) protecting group, an amino group, and a phenyl ring substituted with a bromine atom. This compound is an amino acid derivative, specifically an enantiomer of a chiral amino acid, which is significant in pharmaceutical applications due to its potential biological activity. The presence of the bromine atom on the phenyl ring enhances its reactivity and can influence the compound's interactions in biological systems. The Boc group serves as a protective moiety that can be removed under specific conditions, allowing for further functionalization or incorporation into larger molecules. This compound is typically used in peptide synthesis and medicinal chemistry, where the chirality and functional groups play crucial roles in determining the pharmacological properties of the resulting compounds. Its solubility, stability, and reactivity are influenced by the functional groups present, making it a valuable intermediate in organic synthesis.
Formula:C15H20BrNO4
InChI:InChI=1/C15H20BrNO4/c1-15(2,3)21-14(20)17-12(9-13(18)19)8-10-4-6-11(16)7-5-10/h4-7,12H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t12-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccc(cc1)Br)CC(=O)O)O
Synonyms:
  • (3S)-4-(4-bromophenyl)-3-[(tert-butoxycarbonyl)amino]butanoic acid
  • Boc-β-HoPhe(4-Br)-OH
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