Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for efficient coupling with aryl halides, making it valuable in constructing complex aromatic systems. Commonly employed in the synthesis of bioactive molecules, particularly in drug discovery programs targeting kinase inhibitors and other therapeutic agents. The presence of both boronic acid and methylcarbamoyl groups offers dual reactivity and enhances binding selectivity in medicinal chemistry applications.