66572-41-6

Basic information

• Product Name: Benzamide, N-[2-(3-chlorophenyl)-5-phenyl-2H-1,2,3-triazol-4-yl]-
• CAS NO: 66572-41-6
• Molecular Formula: C21H15ClN4O
• Molecular Weight: 374.829
• Mol File: 66572-41-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[2-(3-chlorophenyl)-5-phenyl-2H-1,2,3-triazol-4-yl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[2-(3-chlorophenyl)-5-phenyl-2H-1,2,3-triazol-4-yl]-(66572-41-6)
• EPA Substance Registry System: Benzamide, N-[2-(3-chlorophenyl)-5-phenyl-2H-1,2,3-triazol-4-yl]-(66572-41-6)

Safety Data

• Hazardous Substances Data: 66572-41-6(Hazardous Substances Data)

Upstream product

• 80815-91-4 N-(3-Chloro-phenyl)-N'-[1-phenyl-1-(5-phenyl-[1,2,4]oxadiazol-3-yl)-meth-(Z)-ylidene]-hydrazine 
• 128102-55-6 phenyl-(5-phenyl-[1,2,4]oxadiazol-3-yl)-methanone (3-chloro-phenyl)-hydrazone 

Relevant articles and documents

Ru(bpy)2Cl2: A catalyst able to shift the course of the photorearrangement in the Boulton-Katritzky reaction

The Boulton-Katritzky reaction represents one of the most popular and efficient strategies used to realize azole-into-azole conversions. For example, under different experimental conditions, it allows the rearrangement of Z-arylhydrazones of 3-benzoyl-5-p

Mononuclear Heterocyclic Rearrangements. Part 13. Substituent Effects on the Rearrangement of Some Z-Arylhydrazones of 3-Benzoyl-5-phenyl-1,2,4-oxadiazole to 2-Aryl-4-benzoylamino-5-phenyl-1,2,3-triazoles in Benzene, Dioxane, Ethyl Acetate, Acetonitrile,

The effects of substituents in the aryl fragment of the Z-arylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole (1) on the rate of the title reaction have been studied at 313.15 K.The results indicate a changeover of mechanism with changing substituent: i