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CAS 145432-51-5

:

(2S,3R)-N-BOC-2-Amino-3-phenylbutyric acid

Description:
(2S,3R)-N-BOC-2-Amino-3-phenylbutyric acid is a chiral amino acid derivative characterized by its specific stereochemistry at the 2 and 3 positions, denoted as (2S,3R). The presence of the tert-butyloxycarbonyl (BOC) protecting group on the nitrogen atom enhances its stability and solubility, making it suitable for various synthetic applications, particularly in peptide synthesis. The phenyl group at the 3-position contributes to its hydrophobic character, influencing its interactions in biological systems. This compound is typically utilized in organic synthesis and medicinal chemistry, where its chiral nature is essential for the development of biologically active molecules. Its CAS number, 145432-51-5, uniquely identifies it in chemical databases, facilitating research and regulatory compliance. As with many amino acid derivatives, it may exhibit properties such as solubility in organic solvents and potential reactivity under specific conditions, making it a valuable intermediate in the synthesis of pharmaceuticals and other complex organic compounds.
Formula:C15H21NO4
Synonyms:
  • (2S,3R)-N-BOC-beta-methylphenylalanine
  • N-BOC-threo-L-beta-methylphenylalanine
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