Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The presence of a tert-butylcarbamoyl group enhances stability and influences electronic properties, improving selectivity in coupling reactions. Commonly employed in the development of active pharmaceutical ingredients (APIs) where chloro-substituted aromatic systems are required as intermediates. Also utilized in materials science for constructing conjugated organic frameworks with tailored electronic characteristics.