Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The presence of fluorine atoms enhances metabolic stability and bioavailability in drug candidates, while the methoxy group contributes to electronic and steric tuning of the target molecule. Commonly employed in the synthesis of bioactive molecules and functional materials requiring specific substitution patterns on aromatic rings.