1263214-82-9

Upstream product

• 3923-52-2 1,1-diphenyl-2-propyn-1-ol 
• 1263214-78-3 2-{4-[4-(hydroxy-diphenyl-methyl)-[1,2,3]triazol-1-yl]-butoxy}-benzoic acid 2-methoxy-ethyl ester 
• 100-46-9 benzylamine 
• 1263214-81-8 2-(4-{4-[benzylamino-bis-(4-methoxy-phenyl)-methyl]-[1,2,3]triazol-1-yl}-butoxy)-benzoic acid 2-methoxy-ethyl ester 
• 1263214-80-7 2-{4-[4-(benzylcarbamoyloxy-diphenyl-methyl)-[1,2,3]triazol-1-yl]-butoxy}-benzoic acid 2-methoxy-ethyl ester 
• 119-61-9 benzophenone 
• 937021-09-5 C₂₇H₃₄N₄O₆ 
• 937021-08-4 benzylcarbamic acid 1,1-dimethylprop-2-ynyl ester 

Downstream Products

• 937021-08-4 benzylcarbamic acid 1,1-dimethylprop-2-ynyl ester 
• 937021-09-5 C₂₇H₃₄N₄O₆ 
• 1263214-73-8 benzyl-carbamic acid 1-methyl-1-phenyl-prop-2-ynyl ester 
• 1263214-80-7 2-{4-[4-(benzylcarbamoyloxy-diphenyl-methyl)-[1,2,3]triazol-1-yl]-butoxy}-benzoic acid 2-methoxy-ethyl ester 
• 1263214-81-8 2-(4-{4-[benzylamino-bis-(4-methoxy-phenyl)-methyl]-[1,2,3]triazol-1-yl}-butoxy)-benzoic acid 2-methoxy-ethyl ester 
• 1263214-78-3 2-{4-[4-(hydroxy-diphenyl-methyl)-[1,2,3]triazol-1-yl]-butoxy}-benzoic acid 2-methoxy-ethyl ester 
• 100-46-9 benzylamine 

Relevant academic research and scientific papers

Novel triazolyl derivatives for acidic release of amines

Triazolyl derivatives of amines were prepared using click chemistry and evaluated as releasing systems in mildly acidic environments. Triazolylcarbamates and alkylamines were obtained, depending on the reactivity of the propargylic intermediates used for the Huisgen cycloaddition. A fast hydrolysis of some derivatives in mildly acidic conditions was achieved. The relative rates were correlated to a proposed mechanism highlighting the complementary role of the triazole ring and carbocation reactivity/stability. Copyright