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 formation of carbon-carbon bonds under mild conditions, making it valuable in drug discovery. The fluorine and acetamido substituents provide sites for further functionalization or influence biological activity, allowing its use as a building block in medicinal chemistry. Commonly applied in the synthesis of kinase inhibitors and other bioactive molecules where fluorinated aromatic structures enhance metabolic stability and binding affinity.