Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in the preparation of complex fluorinated aromatic compounds. Commonly applied in medicinal chemistry for constructing biaryl scaffolds found in bioactive molecules. The presence of both the fluorine atom and the ethylcarbamoyl group allows for enhanced binding selectivity and metabolic stability in drug candidates.