Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the design of bioactive molecules due to the presence of both electron-withdrawing trifluoromethyl and methyl substituents, which enhance metabolic stability and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting enzyme inhibitors. Also explored in agrochemical research for the development of novel herbicides and pesticides owing to its favorable heterocyclic framework.