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N-(diphenyl-λ4-sulfanylidene)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40560-80-3

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40560-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40560-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,6 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40560-80:
(7*4)+(6*0)+(5*5)+(4*6)+(3*0)+(2*8)+(1*0)=93
93 % 10 = 3
So 40560-80-3 is a valid CAS Registry Number.

40560-80-3Relevant academic research and scientific papers

Synthesis of 2-Aminoindoles through Gold-Catalyzed C-H Annulations of Sulfilimines with N-Arylynamides

Tian, Xianhai,Song, Lina,Rudolph, Matthias,Rominger, Frank,Hashmi, A. Stephen K.

supporting information, p. 4327 - 4330 (2019/06/17)

A new gold-catalyzed C-H annulation of sulfilimines with N-phenylynamides is presented. As key intermediates of this operationally simple reaction, the in situ generated α-imino gold carbenes insert into the ortho C-H bonds of the phenyl groups to afford 2-aminoindoles bearing a variety of substitution patterns in high selectivities. This reaction offers a facile approach to biologically important 2-aminoindoles by using inexpensive and readily available starting materials.

Copper-catalyzed imination of sulfoxides and sulfides

Liu, Yuanyuan,Wang, Hanying,Yang, Xianjin

supporting information, p. 4697 - 4702 (2019/07/22)

Sulfoximines and sulfilimines have attracted considerable interest among organic chemists. The Cu(II)-catalyzed imination of sulfoxides and sulfides using various N-fluoro benzenesulfonamides was investigated in this study. The scope of the reaction was demonstrated by using several substituted sulfides and sulfoxides. The flow strategy for the preparation of NH-sulfoximines was also examined. By trapping nitrene intermediates through triphenylphosphine, we found that the reaction was conducted through a metal-nitrene intermediate mechanism.

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