1616980-66-5

Basic information

• Product Name: 2-benzyl-5-(tert-butyl)-3-[3-(trifluoromethyl)benzyl]-1,2,5-thiadiazolidine-1,1-dioxide
• CAS NO: 1616980-66-5
• Molecular Weight: 426.503
• Mol File: 1616980-66-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-benzyl-5-(tert-butyl)-3-[3-(trifluoromethyl)benzyl]-1,2,5-thiadiazolidine-1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-5-(tert-butyl)-3-[3-(trifluoromethyl)benzyl]-1,2,5-thiadiazolidine-1,1-dioxide(1616980-66-5)
• EPA Substance Registry System: 2-benzyl-5-(tert-butyl)-3-[3-(trifluoromethyl)benzyl]-1,2,5-thiadiazolidine-1,1-dioxide(1616980-66-5)

Safety Data

• Hazardous Substances Data: 1616980-66-5(Hazardous Substances Data)

Upstream product

• 1616980-51-8 N-allyl-N’-benzyl-N-tert-butylsulfamide 
• 199188-30-2 3-(trifluoromethyl)phenyl trifluoromethanesulfonate 
• 16486-68-3 N-allyl(tert-butyl)amine 
• 116943-62-5 N-(N'-benzylsulfamoyl)-1,3-oxazolidin-2-one 

Relevant articles and documents

Influence of catalyst structure and reaction conditions on anti- Versus syn-Aminopalladation pathways in pd-catalyzed alkene carboamination reactions of N-Allylsulfamides

The Pd-catalyzed coupling of N-allylsulfamides with aryl and alkenyl triflates to afford cyclic sulfamide products is described. In contrast to other known Pd-catalyzed alkene carboamination reactions, these transformations may be selectively induced to o