Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds with high selectivity. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The protected amino group and fluorine substituent allow for further functionalization or participation in downstream transformations, making it valuable in pharmaceutical and agrochemical research for building complex aromatic structures. Commonly employed in the development of fluorinated drug candidates where precise molecular architecture is critical.