1078739-24-8

Basic information

• Product Name: 4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole
• Synonyms: 4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole
• CAS NO: 1078739-24-8
• Molecular Weight: 329.379
• Mol File: 1078739-24-8.mol
• Article Data: 32

Chemical Properties

• CAS DataBase Reference: 4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole(1078739-24-8)
• EPA Substance Registry System: 4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole(1078739-24-8)

Safety Data

• Hazardous Substances Data: 1078739-24-8(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 5604-42-2 1-(4-methylbenzenesulfonyl)-5-(4-methoxyphenyl)-1,2,3-triazole 
• 941-55-9 4-toluenesulfonyl azide 
• 768-60-5 4-methoxyphenylacetylen 

Downstream Products

• 1149643-73-1 C₂₆H₃₃NO₃S 
• 1209494-89-2 C₁₆H₁₅N₃O₃S 
• 1620645-08-0 C₂₂H₃₁NO₄SSi 
• 1448532-89-5 N¹,N¹-diisopropyl-N²-(4-methylbenzenesulfonyl)-2-(4-methoxyphenyl)acetamidine 
• 64493-71-6 6-(4-methoxyphenyl)-3-phenyl-1,2,4-triazine 

Relevant articles and documents

Efficient synthesis of N-arylsulfonyl-1,2,3-triazoles from 1,1-dibromo-2-arylethylenes

N-arylsulfonyl-1,2,3-triazoles were synthesized from 1,1-dibromo-2-arylethylenes via a one-pot reaction involving the Cs2CO3-mediated dehydrobromination process of the dibromoalkenes to produce alkynes followed by the Cu(I)-catalyzed Huisgen cycloaddition of the alkyne intermediates with tosyl azide.

Diastereoselective N-sulfonylaminoalkenylation of azulenes from terminal alkynes and azides via N-sulfonyl-1,2,3-triazoles

The development of rhodium-catalyzed diastereoselective N-sulfonylaminoalkenylation of azulenes using N-sulfonyltriazoles is described. This procedure can be successfully applied to rhodium-catalyzed diastereoselective N-sulfonylaminoalkenylation of azule

Rhodium-Catalyzed Denitrogenative Transannulation of N-Sulfonyl-1,2,3-triazoles with Glycals Giving Pyrroline-Fused N-Glycosides

Described here is a selective synthesis of 2,3-dihydropyrrole-fused N-glycosides through rhodium-catalyzed denitrogenative transannulation of N-sulfonyl-1,2,3-triazoles with glycals. A series of pyrroline-fused N-glycosides are afforded in moderate to exc

Deoxygenative C2-heteroarylation of quinoline N-oxides: Facile access to α-Triazolylquinolines

A metal-and additive-free, highly efficient, step-economical deoxygenative C2-heteroarylation of quinolines and isoquinolines was achieved from readily available N-oxides and N-sulfonyl-1,2,3-Triazoles. A variety of α-Triazolylquinoline derivatives were synthesized with good regioselectivity and in excellent yields under mild reaction conditions. Further, a gram-scale and one-pot synthesis illustrated the efficacy and simplicity of the developed protocol. The current transformation was also found to be compatible for the late-stage modification of natural products.