Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Also employed in agrochemicals to improve metabolic stability and bioavailability in crop protection agents. The trifluoromethyl and methoxy groups contribute to lipophilicity and electron-withdrawing effects, beneficial for optimizing pharmacokinetic properties in drug design.