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 or vinyl halides, facilitating the construction of biaryl structures. The presence of bromo, fluoro, and butoxy substituents allows for further functionalization or modulation of electronic and steric properties, making it valuable in medicinal chemistry for developing bioactive compounds. Commonly employed in late-stage diversification strategies during drug discovery.