Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of agents with potential antitumor and anti-inflammatory properties. The bromo and trifluoromethyl groups enable selective cross-coupling reactions, making it valuable in building complex molecules for drug discovery. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce aryl or amino substituents. Also utilized in the preparation of fluorescent probes and agrochemicals due to its electron-withdrawing characteristics and stability.