3-(Chloromethyl)-5-(2-(trifluoromethyl)phenyl)-1,2,4-oxadiazole is a chemical compound characterized by its oxadiazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms and three carbon atoms. The presence of a chloromethyl group indicates a reactive site that can participate in further chemical reactions, making it useful in synthetic applications. The trifluoromethyl group attached to the phenyl ring enhances the compound's lipophilicity and can influence its biological activity, often imparting unique properties such as increased potency or selectivity in pharmacological contexts. This compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the trifluoromethyl group, which can affect its reactivity and interactions with other molecules. Additionally, the oxadiazole moiety is known for its applications in materials science and medicinal chemistry, often serving as a scaffold for the development of various bioactive compounds. Overall, this compound's structural features suggest potential utility in diverse chemical and pharmaceutical applications.

3-(CHLOROMETHYL)-5-(2-(TRIFLUOROMETHYL)PHENYL)-1,2,4-OXADIAZOLE

133144-89-5: 3-(Chloromethyl)-5-(2-(trifluoromethyl)phenyl)-1,2,4-oxadiazole is a chemical compound characterized by its oxadiazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms and three carbon atoms. The presence of a chloromethyl group indicates a reactive site that can participate in further chemical reactions, making it useful in synthetic applications. The trifluoromethyl group attached to the phenyl ring enhances the compound's lipophilicity and can influence its biological activity, often imparting unique properties such as increased potency or selectivity in pharmacological contexts. This compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the trifluoromethyl group, which can affect its reactivity and interactions with other molecules. Additionally, the oxadiazole moiety is known for its applications in materials science and medicinal chemistry, often serving as a scaffold for the development of various bioactive compounds. Overall, this compound's structural features suggest potential utility in diverse chemical and pharmaceutical applications.

CAS 133144-89-5

3-(CHLOROMETHYL)-5-(2-(TRIFLUOROMETHYL)PHENYL)-1,2,4-OXADIAZOLE

3-(Chloromethyl)-5-(2-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

Ref: IN-DA0014C8