Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The presence of a fluorine atom and a tert-butylcarbamoyl group enhances substrate selectivity and metabolic stability in drug development. Commonly employed in late-stage functionalization of complex molecules due to its compatibility with various functional groups. Also applied in the preparation of kinase inhibitors and other bioactive molecules where fluorinated aromatic scaffolds are required.