Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in drug discovery and development. Commonly applied in the preparation of bioactive molecules and functional materials where fluorinated and carbamoyl-substituted aromatic systems are needed. Stable and selective under standard coupling conditions, it supports high-yield transformations in medicinal chemistry research.