80535-19-9

Basic information

• Product Name: 1H-1,2,4-Triazolium, 4-(4-methylphenyl)-1-[2-(4-nitrophenyl)-2-oxoethyl]-, bromide
• CAS NO: 80535-19-9
• Molecular Formula: C17H15N4O3.Br
• Molecular Weight: 403.235
• Mol File: 80535-19-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-1,2,4-Triazolium, 4-(4-methylphenyl)-1-[2-(4-nitrophenyl)-2-oxoethyl]-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,4-Triazolium, 4-(4-methylphenyl)-1-[2-(4-nitrophenyl)-2-oxoethyl]-, bromide(80535-19-9)
• EPA Substance Registry System: 1H-1,2,4-Triazolium, 4-(4-methylphenyl)-1-[2-(4-nitrophenyl)-2-oxoethyl]-, bromide(80535-19-9)

Safety Data

• Hazardous Substances Data: 80535-19-9(Hazardous Substances Data)

Upstream product

• 80535-18-8 4-(4-methylphenyl)-4H-1,2,4-triazole 
• 99-81-0 4-Nitrophenacyl bromide 

Downstream Products

• 80535-27-9 3-<2'-carbethoxy-4'-hydroxy-4'-p(nitro-phenyl)-butadienyl-4-(p-tolyl)>-1,2,4-triazole 
• 80535-31-5 3-(1'-p-nitro-benzoyl-2',3'-dicarbomethoxypropenyliden-3')-4-(p-tolyl)-1,2,4-triazolidene-2,3 
• 87688-41-3 4-(p-Tolyl)-1,2,4-triazolium-thioanylido-(p-nitro)-benzoyl-methylure 
• 87688-40-2 4-(p-Tolyl)-1,2,4-triazolium-anylido-(p-nitro)-benzoyl-methylure 
• 87688-38-8 4′-tolyl-1,2,4-triazol-1-ium p-nitrophenacylid 
• 111509-48-9 (5R,6R,7S,7aR)-5-(4-Nitro-benzoyl)-6-phenyl-1-p-tolyl-5,6,7,7a-tetrahydro-1H-pyrrolo[1,2-b][1,2,4]triazole-7-carboxylic acid methyl ester 
• 87688-42-4 4-(p-Tolyl)-1,2,4-triazolium-(N-ethyl-thioamido)-benzoyl-methylure 

Relevant articles and documents

SYNTHESIS AND CHARACTERIZATION OF NEW AZOTRIAZOLIUM YLIDES

Using 1, 3, 4-triazolium salts 8 and diazonium salts 9 by a coupling reaction, new azo-triazolium ylides of the type 10 have been synthetised.All these compounds are strongly coloured.In order to establish the configurations of these products a molecular mechanics procedure has been used.

1,2,4-TRIAZOLIUM-YLURES-V; REACTIONS DES TRIAZOLIUM-PHENACYLURES AVEC LES ALCYNES DISSYMETRIQUES

4-Aryl-1,2,4-triazolium-phenacylides and ethyl propiolate give 3-substituted 4-aryl-1,2,4-triazoles via cycloadducts.