13443-96-4

Basic information

• Product Name: Diazene, benzoyl(4-nitrophenyl)-
• CAS NO: 13443-96-4
• Molecular Formula: C13H9N3O3
• Molecular Weight: 255.233
• Mol File: 13443-96-4.mol

Chemical Properties

• CAS DataBase Reference: Diazene, benzoyl(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Diazene, benzoyl(4-nitrophenyl)-(13443-96-4)
• EPA Substance Registry System: Diazene, benzoyl(4-nitrophenyl)-(13443-96-4)

Safety Data

• Hazardous Substances Data: 13443-96-4(Hazardous Substances Data)

Upstream product

• 3078-09-9 benzaldehyde p-nitrophenylhydrazone 
• 1088-95-5 1-benzoyl-2-(p-nitrophenyl)hydrazine 

Downstream Products

• 74152-75-3 1-(4-nitro-phenyl)-3-phenyl-4a-pyrrolidin-1-yl-4a,5,6,7,8,8a-hexahydro-1H-benzo[1,3,4]oxadiazine 
• 74152-63-9 benzoic acid N'-(2-morpholin-4-yl-cyclohex-1-enyl)-N'-(4-nitro-phenyl)-hydrazide 
• 74152-78-6 7-tert-butyl-1-(4-nitro-phenyl)-3-phenyl-4a-pyrrolidin-1-yl-4a,5,6,7,8,8a-hexahydro-1H-benzo[1,3,4]oxadiazine 
• 74152-66-2 benzoic acid N'-(5-tert-butyl-2-morpholin-4-yl-cyclohex-1-enyl)-N'-(4-nitro-phenyl)-hydrazide 
• 1088-95-5 1-benzoyl-2-(p-nitrophenyl)hydrazine 
• 74152-69-5 4a-morpholin-4-yl-1-(4-nitro-phenyl)-3-phenyl-4a,5,6,7,8,8a-hexahydro-1H-benzo[1,3,4]oxadiazine 
• 74152-72-0 7-tert-butyl-4a-morpholin-4-yl-1-(4-nitro-phenyl)-3-phenyl-4a,5,6,7,8,8a-hexahydro-1H-benzo[1,3,4]oxadiazine 
• 55-21-0 benzamide 
• 106690-01-1 4a-Morpholin-4-yl-1-(4-nitro-phenyl)-3-phenyl-1,4a,5,6,7,7a-hexahydro-cyclopenta[1,3,4]oxadiazine 
• 84999-68-8 Benzoic acid N'-(4-nitro-phenyl)-N'-(3-oxo-2-pyrrolidin-1-yl-cyclohex-1-enyl)-hydrazide 
• 93-58-3 benzoic acid methyl ester 
• 108155-58-4 C₁₆H₁₁Cl₃N₄O₄ 
• 84999-59-7 4a-Morpholin-4-yl-1-(4-nitro-phenyl)-3-phenyl-6,7,8,8a-tetrahydro-1H,4aH-benzo[1,3,4]oxadiazin-5-one 

Relevant articles and documents

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Oxidation of Ketone and Aldehyde Hydrazones, Oximes, and Semicarbazones and of Hydroxylamines and Hydrazo-compounds, using Benzeneselenic Anhydride

Benzeneseleninic anhydride (1; BSA) is an effective reagent for the mild regeneration of the carbonyl group from ketone phenylhydrazones, p-nitrophenylhydrazones, tosylhydrazones, oximes, and semicarbazones at 40-50 deg C.Tosylhydrazones and oximes of aldehydes are also readily converted into the parent aldehyde.The phenylhydrazone and p-nitrophenylhydrazone derivatives of aldehydes afford ketoazo-compounds.The ketoazo-species could also be prepared by oxidation of the corresponding hydrazide with compound (1).Both aromatic and aliphatic hydrazo-compounds and hydroxylamines can be oxidised to azo- and nitrozo-derivatives respectively.