Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated biaryl compounds, particularly in pharmaceutical and agrochemical research. The Boc-protected amine and boronic acid functionalities allow for selective coupling and subsequent deprotection to build complex fluorinated aromatic structures. Commonly employed in the development of kinase inhibitors and other bioactive molecules where fluorine substitution enhances metabolic stability and binding affinity. Its protected amine group enables further derivatization after coupling, making it a valuable building block in medicinal chemistry.