This chemical is primarily utilized in the synthesis of peptides and peptidomimetics due to its role as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group serves as a protective moiety for the amine functionality, allowing selective reactions to occur at other sites of the molecule during peptide coupling processes. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptide chains. Additionally, its stereochemistry makes it useful in the development of chiral molecules, which are essential in pharmaceutical research for creating enantiomerically pure drugs. The benzyl group further enhances its versatility by providing a handle for additional modifications or deprotection strategies.