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Benzenesulfonamide, 2,2'-diselenobis[N-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

217798-91-9

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217798-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217798-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,7,9 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 217798-91:
(8*2)+(7*1)+(6*7)+(5*7)+(4*9)+(3*8)+(2*9)+(1*1)=179
179 % 10 = 9
So 217798-91-9 is a valid CAS Registry Number.

217798-91-9Downstream Products

217798-91-9Relevant academic research and scientific papers

The reactions of 2-(bromoseleno)benzenesulfonyl chloride with primary amines toward 2,2′-diselenobis(benzenesulfonamides) and 1,3,2-benzothiaselenazole 1,1-dioxides: New oxygen-transfer agents, antimicrobials and virucides

Potaczek,Giurg,Kloc,Maliszewska,Piasecki,Pietka,Mlochowski

, p. 687 - 697 (2007/10/03)

The reaction of title compound 6 with primary aliphatic or aromatic amines was investigated. The products were 2,2′-diselenobis(benzenesulfonamides) (4) accompanied in some cases by 1,3,2-benzothiaselenazole 1,1 -dioxides (3). Exceptionally, when aniline was a reagent, 2-(sulfamoylphenyl) phenylselenenylanilide was produced. These results are interpreted in the light of the proposed mechanisms. The compounds 3 and 4 exhibited catalytic activity in hydroperoxide oxidation of cyclohexanone (12) and 1-naphthaldehyde N,N-dimethylhydrazone (17). Although they were inactive against patogenic bacteria and fungi an appreciable antiviral activity against HSV-1 and EMCV of the compounds 3b, 3c and 4b was observed.

Synthesis of organoselenium sulfonamides as new potential cytokine inducers: 2,2'-Diselenobis(benzenesulfonamides) and 1,3,2- benzothiaselenazolone 1,1-dioxides

Kloc, Krystian,Mlochowski, Jacek

, p. 67 - 71 (2007/10/03)

A convenient method for the synthesis of 2,2'- diselenobis(benzenesulfonamides) 4 and 2-substituted 1,3,2- benzothiaselenazole 1,1-dioxides 2, has been elaborated. It is based on the conversion of 2-aminobenzenesulfonic acid into bis[2-(chlorosulfonyl)phe

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