N-(Dimethyloxido-lambda4-sulfanylidene)benzenesulfonamide

Base Information

Chemical Name:N-(Dimethyloxido-lambda4-sulfanylidene)benzenesulfonamide
CAS No.:22236-46-0
Molecular Formula:C8H11NO3S2
Molecular Weight:233.312
Hs Code.:
DSSTox Substance ID:DTXSID901218671

Synonyms:N-(Dimethyloxido-lambda4-sulfanylidene)benzenesulfonamide;DTXSID901218671;22236-46-0

Suppliers and Price of N-(Dimethyloxido-lambda4-sulfanylidene)benzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(Dimethyloxido-lambda4-sulfanylidene)benzenesulfonamide

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:233.01803556
Heavy Atom Count:14
Complexity:385

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Canonical SMILES:CS(=NS(=O)(=O)C1=CC=CC=C1)(=O)C

Technology Process of N-(Dimethyloxido-lambda4-sulfanylidene)benzenesulfonamide

There total 8 articles about N-(Dimethyloxido-lambda4-sulfanylidene)benzenesulfonamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 70.0%

: 19871-30-8
S,S-dimethyl-N-(phenylsulfonyl)sulfimide

: 22236-46-0
N-(dimethyl(oxo)-λ6-sulfanylidene)benzenesulfonamide

Guidance literature:: With peracetic acid; ruthenium(IV) oxide; In dichloromethane; for 1h;

Reference yield: 67.0%

: 67-68-5,8070-53-9
dimethyl sulfoxide

: 145490-75-1
N-fluorobenzene sulfonamide

: 22236-46-0
N-(dimethyl(oxo)-λ6-sulfanylidene)benzenesulfonamide

Guidance literature:: With copper dichloride; In acetone; at 70 ℃; for 12h; Reagent/catalyst; Solvent; Temperature; Catalytic behavior;
DOI:10.1016/j.tet.2019.07.020