Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides, facilitating the construction of biaryl structures. The presence of bromine and trifluoromethoxy groups provides sites for further functionalization and enhances lipophilicity, making it valuable in drug discovery for tuning biological activity and metabolic stability. Commonly employed in the development of bioactive compounds and functional materials.