Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical development. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in constructing biaryl scaffolds found in bioactive compounds. The fluorine and cyclopropylaminomethyl substituents enhance binding selectivity and metabolic stability in drug candidates, especially in oncology and central nervous system therapies. Commonly employed in late-stage functionalization due to its stability and reactivity profile.