Used as an intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation, allowing for the introduction of substituted aryl or heteroaryl groups. Its protected amine functionality (via carbamate) permits further selective modifications downstream, making it valuable in multi-step synthesis of bioactive compounds. Commonly employed in the development of drug candidates where fluorinated and chlorinated aromatic systems are needed for optimal biological activity.