26464-50-6

Upstream product

• 106-49-0 p-toluidine 
• 118985-14-1 p-nitrophenacyl m-nitrobenzenesulphonate 
• 118985-13-0 p-nitrophenacyl p-chlorobenzenesulphonate 
• 115400-13-0 p-nitrophenacyl benzenesulphonate 
• 56177-37-8 1-(4-nitrophenyl)-2-(p-tolylsulfonyloxy)ethanone 
• 99-81-0 4-Nitrophenacyl bromide 

Downstream Products

• 54583-58-3 2-methyl-4-(4-nitro-phenyl)-1-p-tolyl-pyrrole-3-carboxylic acid ethyl ester 
• 88502-19-6 2-Methyl-5-(4-nitro-phenyl)-1-p-tolyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 88502-35-6 5-(4-Amino-phenyl)-2-methyl-1-p-tolyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 97814-21-6 4-(4-Nitro-phenyl)-1-p-tolyl-1H-imidazole 
• 97814-31-8 1-(p-methylphenyl)-4-(p-aminophenyl)imidazole 
• 97814-12-5 4-(4-Nitro-phenyl)-1-p-tolyl-1H-imidazole-2-thiol 

Relevant academic research and scientific papers

Nucleophilic Substitution Reactions of Phenacyl Benzenesulphonates with Anilines in Methanol-Acetonitrile Mixtures

The nucleophilic substitution reactions of phenacyl benzenesulphonates with anilines in methanol-acetonitrile have been studied.A stronger nucleophile was found to cause less bond cleavage, while a better leaving group led to less bond formation, in compl

The Color of N-(4-Nitrophenacyl)arylamines

The N-(4-nitrophenacyl)arylamines 5, prepared from the arylamines 3 and 4-nitrophenacyl bromide (2), have a yellow, red or violet color, depending on the nature of the aryl substituents.The color is explained by intramolecular interaction of the electron accepting nitrobenzoyl group and the electron donating arylamine part of the molecules.On acetylation of the amino group the color is lost.There are no indications for an equilibrium between the amines 5 and N-(4-nitrostyryl)-arylamines 7.