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N-(methyl(4-chlorophenyl)-λ4-sulfanylidene)cyanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28001-55-0

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28001-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28001-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28001-55:
(7*2)+(6*8)+(5*0)+(4*0)+(3*1)+(2*5)+(1*5)=80
80 % 10 = 0
So 28001-55-0 is a valid CAS Registry Number.

28001-55-0Relevant academic research and scientific papers

N-Imidazolylation of Sulfoximines from N-Cyano Sulfoximines, 1-Alkynes, and N-Sulfonyl Azides

Kim, Sanghyuck,Kim, Ji Eun,Lee, Jinsub,Lee, Phil Ho

, p. 3707 - 3717 (2015)

The rhodium-catalyzed N-imidazolylation of N-sulfonyl-1,2,3-triazoles with a variety of N-cyano sulfoximines has been developed for the synthesis of N-imidazolyl sulfoximines via elimination of molecular nitrogen. Copper-catalyzed [3+2] cycloaddition followed by rhodium-catalyzed N-imidazolylation from 1-alkynes, N-sulfonyl azides, and N-cyano sulfoximines is also demonstrated for the synthesis of N-imidazolyl sulfoximines in a one-pot procedure.

Anodic Dehydrogenative Cyanamidation of Thioethers: Simple and Sustainable Synthesis of N-Cyanosulfilimines

Klein, Martin,Waldvogel, Siegfried R.

supporting information, p. 23197 - 23201 (2021/09/25)

A novel and very simple to perform electrochemical approach for the synthesis of several N-cyanosulfilimines in good to excellent yields was established. This method provides access to biologically relevant sulfoximines by consecutive oxidation using electro-generated periodate. This route can be easily scaled-up to gram quantities. The S,N coupling is carried out at an inexpensive carbon anode by direct oxidation of sulfide. Therefore, the designed process is atom economic and represents a new “green route” for the synthesis of sulfilimines and sulfoximines.

Sulfoxide-to-sulfilimine conversions: Use of modified Burgess-type reagents

Hendriks, Christine M. M.,Lamers, Philip,Engel, Julien,Bolm, Carsten

, p. 3363 - 3368 (2013/12/04)

Sulfoxides can directly be converted into N-cyanosulfilimines using a new Burgess-type reagent. By applying this strategy with a related reagent variant, synthetically valuable NH-sulfoximines have been prepared from sulfoxides via N-protected sulfilimines. The practical three-step reaction sequence is generally high yielding and applicable to a wide range of substrates. The sulfoxide-to-sulfilimine conversion can also be performed under solvent-reduced conditions in a ball mill. Copyright

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