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CAS 51871-62-6

:

(S)-3-(Boc-amino)-4-phenylbutyric acid

Description:
(S)-3-(Boc-amino)-4-phenylbutyric acid, with the CAS number 51871-62-6, is a chiral amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino functional group. This compound features a phenyl group attached to the butyric acid backbone, contributing to its hydrophobic characteristics. The Boc group serves as a protective moiety, commonly used in peptide synthesis to prevent unwanted reactions at the amino group. The stereochemistry indicated by the (S) configuration suggests that the molecule exhibits specific spatial arrangements, which can influence its biological activity and interactions. This compound is often utilized in pharmaceutical research and development, particularly in the synthesis of peptide-based drugs or as an intermediate in organic synthesis. Its solubility and reactivity can vary based on the pH and the presence of other functional groups, making it a versatile building block in medicinal chemistry.
Formula:C15H21NO4
InChI:InChI=1S/C15H21NO4/c1-15(2,3)20-14(19)16-12(10-13(17)18)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m0/s1
InChI key:ACKWQHCPHJQANL-LBPRGKRZSA-N
SMILES:CC(C)(C)OC(=O)N[C@@H](CC1=CC=CC=C1)CC(=O)O
Synonyms:
  • (S)-3-(tert-Butyloxycarbonyl)amino-4-phenylbutyric acid
  • Boc-L-Beta-Homophenylalanine
  • Boc-β-HoPhe-OH
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