Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl and aryl-heteroaryl frameworks common in pharmaceuticals and agrochemicals. The boronic acid group enables carbon-carbon bond formation under mild conditions, while the Boc-protected amine allows for selective deprotection and further functionalization. Its bifunctional structure makes it valuable in medicinal chemistry for building complex molecules, especially in the development of drug candidates where controlled reactivity and stability are required. Commonly employed in late-stage diversification strategies due to compatibility with various functional groups.