Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds for pharmaceutical and agrochemical development. Its boronic acid group enables carbon-carbon bond formation under mild conditions, making it valuable in drug discovery. The presence of chlorine, fluorine, and a methoxyethoxy substituent allows fine-tuning of electronic and steric properties, enhancing selectivity and reactivity in target molecules. Commonly employed in the preparation of intermediates for bioactive compounds and functional materials.