606926-42-5

Basic information

• Product Name: N-(4-methylphenylsulfonyl)-4-[(trifluoromethanesulfonyl)oxy]-1,2,3,6-tetrahydropyridine
• Synonyms: N-(4-methylphenylsulfonyl)-4-[(trifluoromethanesulfonyl)oxy]-1,2,3,6-tetrahydropyridine
• CAS NO: 606926-42-5
• Molecular Weight: 385.385
• Mol File: 606926-42-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-(4-methylphenylsulfonyl)-4-[(trifluoromethanesulfonyl)oxy]-1,2,3,6-tetrahydropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methylphenylsulfonyl)-4-[(trifluoromethanesulfonyl)oxy]-1,2,3,6-tetrahydropyridine(606926-42-5)
• EPA Substance Registry System: N-(4-methylphenylsulfonyl)-4-[(trifluoromethanesulfonyl)oxy]-1,2,3,6-tetrahydropyridine(606926-42-5)

Safety Data

• Hazardous Substances Data: 606926-42-5(Hazardous Substances Data)

Upstream product

• 37595-74-7 N,N-phenylbistrifluoromethane-sulfonimide 
• 33439-27-9 N-tosyl-4-piperidone 
• 41979-39-9 4-piperidone hydrochloride 
• 98-59-9 p-toluenesulfonyl chloride 
• 358-23-6 trifluoromethylsulfonic anhydride 

Downstream Products

• 1579291-51-2 4-(2-azidophenyl)-1-tosyl-1,2,3,6-tetrahydropyridine 
• 606926-45-8 4-(4-chloro-2-nitrophenyl)-2-(4-methylsulfonyloxy)-1,2,3,6-tetrahydropyridine 

Relevant articles and documents

Synthesis method of enol trifluoromethanesulfonate

The invention provides a synthesis method of enol trifluoromethanesulfonate, which takes ketone compounds, trifluoromethanesulfonic anhydride, alkali and dichloromethane as raw materials, and generates enol trifluoromethanesulfonate through sectional este

Sequential Suzuki-Miyaura Coupling/Lewis Acid-Catalyzed Cyclization: An Entry to Functionalized Cycloalkane-Fused Naphthalenes

Functionalized angular cycloalkane-fused naphthalenes were prepared using a two-step process involving a Pd-catalyzed Suzuki-Miyaura coupling of aryl pinacol boronates and vinyl triflates followed by a boron trifluoride etherate-catalyzed cycloaromatization.

Development of a Suzuki cross-coupling reaction between 2-azidoarylboronic pinacolate esters and vinyl triflates to enable the synthesis of [2,3]-fused indole heterocycles

The scope and limitations of a Suzuki reaction between 2-azidoarylboronic acid pinacolate esters and vinyl triflates are reported. This cross-coupling reaction enables the regioselective synthesis of indoles after a subsequent RhII2-catalyzed sp2-C-H bond amination reaction.