23269-74-1

Usage

Uses

Used in Pharmaceutical Industry:
1-(1-Phenylvinyl)-1H-benzo[d][1,2,3]triazole is used as a compound in the development of pharmaceuticals for its potential applications in medicinal chemistry. Its unique structure allows for the creation of various functionalized compounds that can be utilized in the treatment of different medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1-Phenylvinyl)-1H-benzo[d][1,2,3]triazole is used as a compound in the development of agrochemicals. Its properties make it a promising candidate for the creation of new products that can enhance agricultural productivity and protect crops from pests and diseases.
Used in Organic Synthesis:
1-(1-Phenylvinyl)-1H-benzo[d][1,2,3]triazole is used as a building block in organic synthesis for the preparation of various functionalized compounds. Its unique structure and properties make it a valuable tool for researchers in the synthesis of new molecules with potential applications in various fields.
Used in Research and Development:
1-(1-Phenylvinyl)-1H-benzo[d][1,2,3]triazole is used as a research tool for studying the biological and pharmacological activities of triazole derivatives. Its chemical structure allows researchers to explore its potential in understanding the mechanisms of action and developing new therapeutic strategies.

Upstream product

• 100-42-5 styrene 
• 95-14-7 1,2,3-Benzotriazole 
• 16717-64-9 1-azidostyrene 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 536-74-3 phenylacetylene 

Downstream Products

• 451-40-1 phenyl benzyl ketone 
• 95-14-7 1,2,3-Benzotriazole 
• 5399-30-4 2-oxo-2-phenylethylthiocyanate 
• 31378-03-7 1-phenyl-2-tosylethanone 
• 709-21-7 3,3,3-trifluoro-1-phenylpropan-1-one 
• 18503-48-5 2-(tert-butyl)quinoxaline 
• 40115-00-2 2-cyclohexyl-quinoxaline 
• 1684-14-6 2,3-diphenylquinoxaline 
• 105702-07-6 2-(2-methylphenyl)quinoxaline 
• 27993-83-5 2-(3-chlorophenyl)quinoxaline 
• 5021-45-4 2-(4-bromophenyl)quinoxaline 
• 449-46-7 2-(4-fluorophenyl)quinoxaline 
• 5021-46-5 2-(4-methoxyphenyl)quinoxaline 
• 1350516-03-8 2-(4-ethylphenyl)quinoxaline 

Relevant academic research and scientific papers

Synthesis of 1-(2-bromo-1-arylethyl)-1H-benzotriazoles via NBS promoted addition of 1H-benzotriazole to alkene: Relevance in benzotriazole ring cleavage

A cost-effective and expeditious one-pot synthesis of 1-(2-bromo-1-arylethyl)-1H-benzotriazoles has been devised by reacting styrene and their derivatives with 1H-benzotriazole in presence of N-bromosuccinimide in anhydrous CH2Cl2 at room temperature. Further, the resulted compounds undergo E2-ellimination to afford the respective 1-(1-aryl-vinyl)-1H-benzotriazoles. At the end, 1-(1-phenylvinyl)-1H-benzotriazoles underwent benzotriazole ring cleavage (BtRC) under free radical condition to produce phenanthridine as the final product.

An organoselenium-catalyzed N1- And N2-selective aza-Wacker reaction of alkenes with benzotriazoles

An organoselenium-catalyzed N1- and N2-selective aza-Wacker reaction of alkenes with benzotriazoles is reported, which provides easy access to N1- and N2-olefinated benzotriazole derivatives. The wide substrate

Ambient benzotriazole ring opening through intermolecular radical addition to vinyltriazole

Radical addition to vinyltriazole was developed as a new approach to achieve 1,2,3-triazole ring opening under mild conditions. Through reagent control, excellent chemoselectivity was achieved, giving either nitrile under basic conditions or quinoxaline under neutral conditions. Reactivities made this method an attractive new reaction mode.

Highly efficient synthesis of vinyl substituted triazoles by Au(I) catalyzed alkyne activation

Au(I) catalyzed 1,2,3-triazole addition to non-activated alkyne was reported. A large group of substituted NH-1,2,3-triazoles were suitable for this transformation along with both internal and terminal alkynes. The N-1 and N-2 vinyl substituted 1,2,3-tria

Benzyne click chemistry: Synthesis of benzotriazoles from benzynes and azides

(Chemical Equation Presented) A variety of substituted benzotriazoles have been prepared by the [3 + 2] cycloaddition of azides to benzynes. The reaction scope is quite general, affording a rapid and easy entry to substituted, functionalized benzotriazoles under mild conditions.