96239-00-8

Upstream product

• 21151-56-4 p-chlorophenoxymethyl chloride 
• 122-88-3 4-Chlorophenoxyacetic acid 

Downstream Products

• 96239-22-4 1-(4-Chloro-phenoxymethyl)-4-phenyl-1H-[1,2,3]triazole 
• 96239-21-3 1-(4-Chloro-phenoxymethyl)-5-phenyl-1H-[1,2,3]triazole 
• 96239-19-9 1-(4-Chloro-phenoxymethyl)-4,5-diphenyl-1H-[1,2,3]triazole 
• 96239-17-7 1-(4-Chloro-phenoxymethyl)-1H-[1,2,3]triazole-4,5-dicarboxylic acid diethyl ester 

Relevant academic research and scientific papers

Silver-Catalyzed Decarboxylative Radical Azidation of Aliphatic Carboxylic Acids in Aqueous Solution

We report herein an efficient and general method for the decarboxylative azidation of aliphatic carboxylic acids. Thus, with AgNO3 as the catalyst and K2S2O8 as the oxidant, the reactions of various aliphatic carboxylic acids with tosyl azide or pyridine-3-sulfonyl azide in aqueous CH3CN solution afforded the corresponding alkyl azides under mild conditions. A broad substrate scope and wide functional group compatibility were observed. A radical mechanism is proposed for this site-specific azidation.

Preparation d'aryloxymethyl-1 triazoles-1,2,3

The preparation of 1-aryloxymethyl-1,2,3-triazoles, potential biologically active compounds particularly in the pesticide field, is described.The action of sodium azide on aryloxymethyl halides gave aryloxymethyl azides.The cycloaddition reactions of azid