Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in drug discovery. The presence of amino and fluoro substituents enhances binding selectivity and metabolic stability in target molecules. Commonly employed in the preparation of intermediates for anticancer, antiviral, and anti-inflammatory agents.