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[N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane

Base Information
  • Chemical Name:[N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane
  • CAS No.:236122-13-7
  • Molecular Formula:C11H18INO2SSi
  • Molecular Weight:383.325
  • Hs Code.:
  • Mol file:236122-13-7.mol
[N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane

Synonyms:[N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane

Suppliers and Price of [N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of [N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane
Chemical Property:
  • PSA:54.88000 
  • LogP:4.75930 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Physical properties mp 84–85.5 °C.
  • Uses [N-(2-(Trimethylsilyl)ethanesulfonyl)- imino]phenyliodane is a iodine(III) reagent used as a nitrogen atom source in the transition-metal catalyzed aziridination of olefins or in the sulfoximination of sulfoxides. It participates in the reactions of Copper-Catalyzed Aziridination of Olefins, Sulfoximination of Sulfoxides, etc.
Technology Process of [N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane

There total 1 articles about [N-(2-(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With potassium hydroxide; In methanol; 1.) 0 deg C, 30 min, 2.) 20 deg C, 3 h;
DOI:10.1021/jo990356x
Guidance literature:
tetrakis(acetonitrile)copper(I) hexafluorophosphate; In acetonitrile; at 0 - 20 ℃; for 20h;
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