Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds for pharmaceutical and agrochemical development. The boronic acid group enables carbon-carbon bond formation under mild conditions, while the Boc-protected aminomethyl group allows for further functionalization or deprotection in multistep syntheses. Commonly employed in the preparation of bioactive molecules and drug intermediates where controlled reactivity and functional group compatibility are essential.