Used in Suzuki-Miyaura cross-coupling reactions to synthesize fluorinated biaryl compounds, which are valuable in pharmaceutical and agrochemical research due to their enhanced metabolic stability and lipophilicity. The presence of both cyano and trifluoromethyl groups makes this boronic acid a versatile building block for creating bioactive molecules. It is particularly useful in the development of drug candidates targeting central nervous system disorders and anti-inflammatory agents. Its boronic acid functionality allows for efficient palladium-catalyzed coupling with aryl halides under mild conditions, enabling rapid diversification of molecular structures in medicinal chemistry workflows.