Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. The presence of sulfanyl and nitrile groups allows for further functionalization, enabling derivatization to optimize drug-like properties. Commonly employed in medicinal chemistry research for generating analogs in structure-activity relationship (SAR) studies. Also utilized in agrochemical research for designing bioactive molecules with pesticidal or fungicidal activity due to its stable aromatic framework and electron-withdrawing trifluoromethyl group.