23572-06-7

Basic information

• Product Name: Methanone, phenyl(5-phenyl-1,2,4-oxadiazol-3-yl)-
• CAS NO: 23572-06-7
• Molecular Formula: C15H10N2O2
• Molecular Weight: 250.257
• Mol File: 23572-06-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanone, phenyl(5-phenyl-1,2,4-oxadiazol-3-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, phenyl(5-phenyl-1,2,4-oxadiazol-3-yl)-(23572-06-7)
• EPA Substance Registry System: Methanone, phenyl(5-phenyl-1,2,4-oxadiazol-3-yl)-(23572-06-7)

Safety Data

• Hazardous Substances Data: 23572-06-7(Hazardous Substances Data)

Upstream product

• 95390-15-1 5-nitroso-2,4-diphenyl-imidazole 
• 7647-01-0 hydrogenchloride 
• 100-47-0 benzonitrile 
• 536-74-3 phenylacetylene 
• 614-21-1 2-nitroacetophenone 
• 98-86-2 acetophenone 
• 103404-02-0 bis-[phenyl-(5-phenyl-[1,2,4]oxadiazol-3-yl)-methylene]-hydrazine 

Relevant articles and documents

Iron Nitrate-Mediated Selective Synthesis of 3-Acyl-1,2,4-oxadiazoles from Alkynes and Nitriles: The Dual Roles of Iron Nitrate

A direct strategy for the selective synthesis of 3-acyl-1,2,4-oxadiazoles from alkynes and nitriles has been developed under iron(III) nitrate-mediated conditions. The mechanism includes three sequential procedures: Iron(III) nitrate-mediated nitration of

Lanthanide nitrates as lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives

In this work we report the use of lanthanide nitrates [Ln(NO 3)3] acting as catalyst in direct one-pot synthesis of 3-benzoyl- and 3-acetyl-1,2,4-oxadiazoles derivatives from ketones, nitriles and nitric acid. This is the first examp