169338-57-2

Basic information

• Product Name: N-(5-Methyl-[1,2,4]oxadiazol-3-yl)-3-trifluoromethyl-benzamide
• Synonyms: N-(5-Methyl-[1,2,4]oxadiazol-3-yl)-3-trifluoromethyl-benzamide
• CAS NO: 169338-57-2
• Molecular Weight: 271.199
• Mol File: 169338-57-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(5-Methyl-[1,2,4]oxadiazol-3-yl)-3-trifluoromethyl-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(5-Methyl-[1,2,4]oxadiazol-3-yl)-3-trifluoromethyl-benzamide(169338-57-2)
• EPA Substance Registry System: N-(5-Methyl-[1,2,4]oxadiazol-3-yl)-3-trifluoromethyl-benzamide(169338-57-2)

Safety Data

• Hazardous Substances Data: 169338-57-2(Hazardous Substances Data)

Upstream product

• 40483-47-4 5-methyl-[1,2,4]oxadiazol-3-ylamine 
• 2251-65-2 3-(Trifluoromethyl)benzoyl chloride 

Relevant articles and documents

Studies on azole-to-azole interconversions. Substituent effects on the ring-degenerate equilibration between 3-aroylamino-5-methyl-1,2,4-oxadiazoles and 3-acetylamino-5-aryl-1,2,4-oxadiazoles

The title reaction has been studied both in CD3OD and (t)BuOK/CD3OD by means of 1H NMR measurements. The equilibrium composition and the effect exerted thereon by X-substituents in the aryl moiety have been found to be quite different whether neutral or anionic forms are involved. In the first case the effect of X is meager and 3-acetylamino-1,2,4-oxadiazoles are more stable than the 3-aroylamino-5-methyl isomers. Vice-versa, when anions are involved the substituent effect is remarkable and the equilibrium can be, for strongly electron-withdrawing X-groups, even largely shifted towards the anions of the 3-aroylamino-5-methyl-1,2,4-oxadiazoles.