99590-19-9

Basic information

• Product Name: ethyl 1-(4-nitrobenzyl)-1H-1,2,3-triazole-4-carboxylate
• Synonyms: ethyl 1-(4-nitrobenzyl)-1H-1,2,3-triazole-4-carboxylate
• CAS NO: 99590-19-9
• Molecular Weight: 276.252
• Mol File: 99590-19-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: ethyl 1-(4-nitrobenzyl)-1H-1,2,3-triazole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-(4-nitrobenzyl)-1H-1,2,3-triazole-4-carboxylate(99590-19-9)
• EPA Substance Registry System: ethyl 1-(4-nitrobenzyl)-1H-1,2,3-triazole-4-carboxylate(99590-19-9)

Safety Data

• Hazardous Substances Data: 99590-19-9(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 99590-42-8 1--benzyl>-1H-1,2,3-triazole 
• 99590-41-7 1--1H-1,2,3-triazole 
• 99590-30-4 1--1H-1,2,3-triazole 
• 99590-40-6 1--benzyl>-1H-1,2,3-triazole 
• 99590-38-2 1-(p-N-benzoylaminobenzyl)-1H-1,2,3-triazole 
• 99590-39-3 1--1H-1,2,3-triazole 
• 99590-31-5 1--1H-1,2,3-triazole 
• 99590-36-0 1--1H-1,2,3-triazole 
• 99590-28-0 1-(p-acetyloxybenzyl)-1H-1,2,3-triazole 
• 99590-33-7 1--1H-1,2,3-triazole 
• 99590-34-8 1--1H-1,2,3-triazole 
• 99590-29-1 1-(p-benzoyloxybenzyl)-1H-1,2,3-triazole 
• 99590-37-1 1-(p-N,N-diacetylaminobenzyl)-1H-1,2,3-triazole 
• 99590-35-9 1--1H-1,2,3-triazole 

Relevant articles and documents

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

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

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