1311386-87-4

Basic information

• Product Name: 4-(1-(2,4-difluorophenyl))-1-benzyl-1,2,3-triazole
• Synonyms: 4-(1-(2,4-difluorophenyl))-1-benzyl-1,2,3-triazole
• CAS NO: 1311386-87-4
• Molecular Weight: 271.269
• Mol File: 1311386-87-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-(1-(2,4-difluorophenyl))-1-benzyl-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1-(2,4-difluorophenyl))-1-benzyl-1,2,3-triazole(1311386-87-4)
• EPA Substance Registry System: 4-(1-(2,4-difluorophenyl))-1-benzyl-1,2,3-triazole(1311386-87-4)

Safety Data

• Hazardous Substances Data: 1311386-87-4(Hazardous Substances Data)

Upstream product

• 622-79-7 benzyl azide 
• 302912-34-1 2,4-difluoroethynylbenzene 
• 100-39-0 benzyl bromide 
• 348-57-2 2,4-difluorobromobenzene 
• 480438-92-4 [(2,4-difluorophenyl)ethynyl]trimethylsilane 

Downstream Products

• 1438890-64-2 Λ-(iridium(III) bis[1′-(4′,6′-difluorophenyl)1,2,3-triazolato-N,C^2′]-4,4′-bi-1H-1,2,3-triazole 1,1′-bis(phenylmethyl)) hexafluorophosphate 

Relevant articles and documents

Iridium(iii)-surfactant complex immobilized in mesoporous silica via templated synthesis: A new route to optical materials

In this work we report the preparation of a new blue-emitting material based on the templated synthesis of mesoporous silica (MCM-41) using micellar solutions of the newly synthesized monocationic metallosurfactant complex bis[1-benzyl-4-(2,4-difluorophen

An efficient Cu-catalyzed azide-alkyne cycloaddition (CuAAC) reaction in aqueous medium with a zwitterionic ligand, betaine

Cu-catalyzed azide-alkyne cycloaddition reaction in aqueous medium was dramatically accelerated by a simple zwitterionic additive, betaine, at ambient temperature. In the presence of betaine, 1,4-disubstituted-1,2,3-triazoles were obtained from azides and

One-pot click synthesis of 1N-alkyl-4-aryl-1,2,3-triazoles from protected arylalkynes and alkyl bromides

1N-Alkyl-4-aryl-1,2,3-triazoles have been prepared through a multicomponent one-pot protocol from the corresponding (arylethynyl)trimethylsilanes and alkyl bromides. In situ alkyl azide formation and alkyne deprotection followed by copper(I)-catalyzed click cycloaddition afforded the desired 1,4-disubstituted 1,2,3-triazoles in generally good to excellent yield, with only minor observation of the undesired 1,5-regioisomeric cycloadduct. The protocol eliminates the need to use reactive organic azides and terminal alkynes. Georg Thieme Verlag Stuttgart. New York.