Used as a key intermediate in the synthesis of antifungal agents, particularly in the development of structurally modified imidazole derivatives. Its trifluoromethyl and chlorophenyl groups enhance lipophilicity and bioavailability, making it valuable in medicinal chemistry for optimizing drug candidates targeting fungal infections. Also investigated for anti-inflammatory and anticancer activities due to its ability to modulate enzyme activity and cellular pathways. Employed in research settings to explore structure-activity relationships in heterocyclic compounds.