1178899-17-6

Basic information

• Product Name: N-acetyl-S-phenyl-S-(trifluoromethyl)sulfilimine
• Synonyms: N-acetyl-S-phenyl-S-(trifluoromethyl)sulfilimine
• CAS NO: 1178899-17-6
• Molecular Weight: 235.23
• Mol File: 1178899-17-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-acetyl-S-phenyl-S-(trifluoromethyl)sulfilimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-acetyl-S-phenyl-S-(trifluoromethyl)sulfilimine(1178899-17-6)
• EPA Substance Registry System: N-acetyl-S-phenyl-S-(trifluoromethyl)sulfilimine(1178899-17-6)

Safety Data

• Hazardous Substances Data: 1178899-17-6(Hazardous Substances Data)

Upstream product

• 71-43-2 benzene 
• 703-18-4 phenyl trifluoromethyl sulfoxide 
• 75-05-8 acetonitrile 

Downstream Products

• 1178899-38-1 N-[oxidophenyl(trifluoromethyl)-λ⁴-sulfanylidene]-acetamide 
• 95414-68-9 imino(phenyl)(trifluoromethyl)-λ⁶-sulfanone 
• 1058685-73-6 N,N-(dimethylamino)-S-phenyl-S-trifluoromethyloxosulfonium trifluoromethanesulfonate 
• 1046786-09-7 N-methyl-S-phenyl-S-trifluoromethylsulfoximine 
• 1335014-75-9 oxophenyl(phenylimino)(trifluoromethyl)-λ⁶-sulfane 

Relevant articles and documents

Structure and Reactivity of N-Heterocyclic Alkynyl Hypervalent Iodine Reagents

Ethynylbenziodoxol(on)e (EBX) cyclic hypervalent iodine reagents have become popular reagents for the alkynylation of radicals and nucleophiles, but only offer limited possibilities for further structure and reactivity fine-tuning. Herein, the synthesis o

Merging hypervalent iodine and sulfoximine chemistry: A new electrophilic trifluoromethylation reagent

Electrophilic trifluoromethylation is at the forefront of methodologies available for the installation of the CF3 moiety to organic molecules; research in this field is largely spurred by the availability of stable and accessible trifluoromethy

Aromatic and benzylic C-H bond functionalization upon reaction between nitriles and perfluoroalkyl sulfoxides

We studied the thermal behavior of some intermediates formed by reaction of nitriles with perfluoroalkyl sulfoxides upon trifluoromethanesulfonic anhydride activation. Bistriflate ketal 3, precursor of sulfilimine 1, may undergo a rearrangement to sulfany