32295-71-9

Basic information

• Product Name: Diazenecarbonitrile, (4-nitrophenyl)-, (E)-
• CAS NO: 32295-71-9
• Molecular Formula: C7H4N4O2
• Molecular Weight: 176.134
• Mol File: 32295-71-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Diazenecarbonitrile, (4-nitrophenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Diazenecarbonitrile, (4-nitrophenyl)-, (E)-(32295-71-9)
• EPA Substance Registry System: Diazenecarbonitrile, (4-nitrophenyl)-, (E)-(32295-71-9)

Safety Data

• Hazardous Substances Data: 32295-71-9(Hazardous Substances Data)

Upstream product

• 93680-31-0 N-(4-nitro-phenyl)-N'-(1H-tetrazol-5-yl)-triazene 
• 151-50-8 potassium cyanide 
• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 58468-75-0 (4-nitro-phenyl)-cis-diazenecarbonitrile 
• 71-43-2 benzene 
• 64-17-5 ethanol 

Downstream Products

• 69924-83-0 (4-nitro-phenyl)-diazenecarboxylic acid amide 
• 73227-38-0 1-(4-nitrophenyl)-2-cyano-1,2-diazabicyclo<2.2.1>hept-4-ene 
• 79828-12-9 1-(4-nitrophenyl)-2-cyano-1,2-diazabicyclo<2.2.2>oct-4-ene 
• 79828-04-9 1-(4-nitrophenyl)-2-cyano-1,2,3,6-tetrahydropyridazine 
• 73227-45-9 1-(4-nitrophenyl)-2-cyano-4,5-dimethyl-1,2,3,6-tetrahydropyridazine 
• 76649-75-7 (4-nitro-phenyl)-diazenecarboxylic acid 
• 79828-11-8 1-(4-nitrophenyl)-2-cyano-4-methyl-1,2,3,6-tetrahydropyridazine 
• 52569-45-6 N-hydroxy-2t-(4-nitro-phenyl)-diazenecarboximidic acid amide 
• 32263-75-5 [1,2]naphthoquinone-1-(4-nitro-phenylimine) 
• 32249-64-2 N-cyano-2-(4-nitro-phenyl)-diazenecarbonimidic acid amide 

Relevant articles and documents

Reaction of 3-Aryl-1-(tetrazol-5'-yl)triazines with some Electrophiles: Mercury Derivatives and Fragmentations: A New Route to Aryl Diazocyanides

Treatment of 3-aryl-1-(tetrazol-5'-yl)triazines (4) with lead tetra-acetate resulted in a fragmentation to aryl-diazocyanides.The triazines (4) and their monomethyl derivatives when treated with mercuric acetate and phenylmercury hydroxide gave stable mer

Phase-Transfer Synthesis of Arenediazocyanides and Synthesis of Arenediazosulfones from Arenediazonium Cations and the Formation of Reduced Pyridazines by 2 + 4 Cycloaddition Reactions

The remarkably versatile arenediazonium cations are also convenient to use and nondangerous when utilized as the BF4 or PF6 salts.Arenediazonium compounds have recently been shown to undergo the 2 + 4 Diels-Alder cycloaddition, but the reaction is solvent