99590-19-9

Upstream product

• 100-14-1 4-nitrobenzyl chloride 
• 623-47-2 propynoic acid ethyl ester 
• 17271-88-4 p-nitrobenzyl azide 

Downstream Products

• 99590-22-4 1-(p-nitrobenzyl)-1H-1,2,3-triazole-4-carboxylic acid 
• 99590-32-6 1--benzyl>-1H-1,2,3-triazole 
• 99590-17-7 1--benzyl>-1H-1,2,3-triazole 
• 99590-26-8 1-(p-amino-benzyl)-1H-1,2,3-triazole 
• 99590-27-9 1-(p-hydroxy-benzyl)-1H-1,2,3-triazole 
• 99590-25-7 1-(1,2,3-traizol-1-ylmethyl)-4-nitrobenzene 
• 99590-35-9 1--1H-1,2,3-triazole 
• 99590-37-1 1-(p-N,N-diacetylaminobenzyl)-1H-1,2,3-triazole 
• 99590-29-1 1-(p-benzoyloxybenzyl)-1H-1,2,3-triazole 
• 99590-34-8 1--1H-1,2,3-triazole 
• 99590-33-7 1--1H-1,2,3-triazole 
• 99590-28-0 1-(p-acetyloxybenzyl)-1H-1,2,3-triazole 
• 99590-36-0 1--1H-1,2,3-triazole 
• 99590-31-5 1--1H-1,2,3-triazole 

Relevant academic research and scientific papers

Regioselective synthesis of 1,4-disubstituted triazoles using bis[(L)prolinato-N,O]Zn complex as an efficient catalyst in water as a sole solvent

A concise, convenient and mild route for one-pot regioselective synthesis of N-aryl- and N-alkyltriazoles in water as a sole solvent is reported. The methodology involves a three-component reaction comprising aryl/alkyl-alkyne, sodium azide and aryl/alkyl

An efficient and recyclable thiourea-supported copper(i) chloride catalyst for azide-alkyne cycloaddition reactions

A reaction between two equivalents of bulky thiourea, i.e., 1,3-bis(2,6-dimethylphenyl)thiourea (L) [L = (ArNH)2C = S; Ar = 2,6-Me2C6H3], and CuCl2 or CuCl in THF solvent afforded a bulky thiourea-sta

Heteroleptic bis(N-heterocyclic carbene)copper(I) complexes: Highly efficient systems for the [3+2] cycloaddition of azides and alkynes

The first examples of heteroleptic bis-N-heterocyclic carbene (NHC) copper(I) complexes and a mixed NHC-phosphine Cu complex are reported. These complexes are easily synthesized from the reaction of [Cu(OH)(NHC)] with various imidazol(idin)ium or phosphon

Dipolar Cycloaddition Reactions of Organic Azides with some Acetylenic Compounds

Phenyl azide 1 and several substituted benzyl azides 2a-o underwent 1,3-dipolar cycloaddition reactions with dimethyl acrtylenedicarboxylate 3, phenylacetylene 4 and ethyl propiolate 5 to afford the triazoles 6-13.The reactions of these azides with ethyl

1-(4-Substituted-benzyl)-1,2,3-triazoles, in vitro inhibitors of prostaglandin synthesis

This paper describes the preparation of some 1-(4-substituted-benzyl)-1,2,3-triazole derivatives from 4-nitrobenzyl azide by 1,3-dipolar cycloaddition, functional group conversion and nucleophilic substitution reactions. Evaluation of these compounds as i