Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of bioactive molecules with antimicrobial and anti-inflammatory properties. Its structure supports the design of enzyme inhibitors due to the electron-withdrawing fluorine atom and the reactive oxadiazolone ring. Commonly employed in medicinal chemistry for constructing heterocyclic compounds that enhance metabolic stability and binding affinity. Also applied in agrochemical research for developing novel pesticides with improved efficacy and selectivity.