(S)-3-Phenylalanine t-butyl ester is an amino acid derivative characterized by its chiral nature, specifically the (S) configuration at the alpha carbon. This compound features a phenyl group attached to the beta carbon, contributing to its aromatic properties. The t-butyl ester functional group enhances its lipophilicity, making it more soluble in organic solvents compared to its free acid form. This esterification also plays a crucial role in protecting the amino group during synthetic processes, facilitating various chemical reactions, including peptide synthesis. The compound is often utilized in pharmaceutical and biochemical research due to its potential applications in drug development and as a building block in peptide synthesis. Its molecular structure allows for specific interactions in biological systems, making it of interest in studies related to protein folding and enzyme activity. As with many amino acid derivatives, it is important to handle this compound with care, adhering to safety protocols due to its potential reactivity and biological activity.

(S)-3-PHENYLALANINE T-BUTYL ESTER

16874-17-2: L-Phenylalanine-T-Butyl Ester, (S)-3-Phenylalaninetert-butylester

CAS 16874-17-2: (S)-3-PHENYLALANINE T-BUTYL ESTER

(S)-tert-Butyl 2-amino-3-phenylpropanoate

Ref: 10-F690577

(S)-tert-Butyl 2-amino-3-phenylpropanoate

Ref: 54-OR90527

L-Phenylalanine, 1,1-dimethylethyl ester

Ref: IN-DA001Y9T