118946-84-2

Upstream product

• 118946-58-0 5-(4-Chloro-phenyl)-3-phenyl-3H-[1,2,3]triazol-4-ylamine 
• 118946-70-6 5-azido-4-(p-chlorophenyl)-1-phenyl-1,2,3-triazole 
• 140-53-4 p-chlorobenzyl cyanide 
• 622-37-7 Phenyl azide 

Downstream Products

• 118946-86-4 N-phenyl-α,α-dimethoxy-(p-chloro)phenylacetamidine 
• 126158-82-5 [5-Amino-3-(4-chloro-phenyl)-4-phenyl-pyrrol-(2Z)-ylidene]-phenyl-amine 
• 126158-90-5 2-(p-Chlorophenyl)-3-phenylmaleimide 
• 126158-73-4 (E)-2-(4-Chloro-phenyl)-3-cyano-3,N-diphenyl-acrylamidine 

Relevant academic research and scientific papers

The Chemistry of 3-(α-Cyanobenzylidene)-1-phenyltriazenes and Their Conversion to Diarylmaleimides and Phenanthrene-9,10-dicarboximides

3-(α-Cyanobenzylidene)-1-phenyltriazine (3a), the product of thermolysis of 5-azido-1,4-diphenyl-1,2,3-triazole (2), is attacked by nucleophilic reagents at the azomethine carbon.Alcohols and phenol give rise to acetals of the N-phenylamidine of phenylgly

SYNTHESIS AND THERMOLYSIS OF 4-SUBSTITUTED 5-AZIDO-1-PHENYL-1,2,3-TRIAZOLES

5-Azido-1-phenyltriazoles (4) can thermally isomerize to diazo substituted tetrazoles (5) or decompose to alkylidenetriazenes (8) depending on the nature of the substituent at the 4-position.The former are obtained for electron-withdrawing substituents (C