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 electron-withdrawing trifluoromethyl and sulfonyl groups contribute to enhanced lipophilicity and resistance to degradation, making it valuable in designing molecules with improved pharmacokinetic profiles.