Widely used in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions without side-chain interference. The Boc (tert-butoxycarbonyl) group provides acid-labile protection for the amine functionality, allowing for controlled deprotection under mild acidic conditions. This makes it valuable in solid-phase and solution-phase peptide assembly, especially in the production of complex biomolecules and pharmaceutical intermediates. Its stability under basic conditions and compatibility with various coupling reagents enhance its utility in multi-step organic syntheses.