Boc-D-4-tert-butyl-Phe, also known as Boc-D-4-tert-butylphenylalanine, is a protected form of the amino acid phenylalanine, specifically the D-enantiomer. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, facilitating its use in peptide synthesis by preventing unwanted reactions. The presence of the tert-butyl group at the para position of the phenyl ring enhances the hydrophobic character of the molecule, which can influence its interactions in biological systems and its solubility in organic solvents. This compound is typically utilized in the field of peptide chemistry and drug development, particularly in the synthesis of peptides where stereochemistry is crucial. Its stability under various conditions makes it a valuable intermediate in organic synthesis. Additionally, the compound's unique structural features contribute to its potential applications in medicinal chemistry and biochemistry, where the manipulation of amino acid properties is essential for designing bioactive molecules.

Boc-D-4-tert-butyl-Phe

250611-12-2: Boc-D-4-tert-butyl-Phe, also known as Boc-D-4-tert-butylphenylalanine, is a protected form of the amino acid phenylalanine, specifically the D-enantiomer. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, facilitating its use in peptide synthesis by preventing unwanted reactions. The presence of the tert-butyl group at the para position of the phenyl ring enhances the hydrophobic character of the molecule, which can influence its interactions in biological systems and its solubility in organic solvents. This compound is typically utilized in the field of peptide chemistry and drug development, particularly in the synthesis of peptides where stereochemistry is crucial. Its stability under various conditions makes it a valuable intermediate in organic synthesis. Additionally, the compound's unique structural features contribute to its potential applications in medicinal chemistry and biochemistry, where the manipulation of amino acid properties is essential for designing bioactive molecules.

CAS 250611-12-2

Boc-D-4-tert-butyl-Phe

Boc-d-4-tert-butylphenylalanine

Ref: IN-DA002QB6

Boc-4-tert-butyl-D-Phe-OH

Ref: 7W-GM5365

(R)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid

Ref: 10-F241393