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 coupling with aryl halides, making it valuable in creating biaryl compounds for drug discovery. The sulfamoyl group enhances solubility and can influence biological activity, allowing its use in designing enzyme inhibitors and bioactive molecules. Commonly employed in medicinal chemistry for lead optimization and library synthesis.