4-Methyl-N-(oxidodiphenyl-lambda4-sulfanylidene)benzenesulfonamide

Base Information

Chemical Name:4-Methyl-N-(oxidodiphenyl-lambda4-sulfanylidene)benzenesulfonamide
CAS No.:38764-58-8
Molecular Formula:C₁₉H₁₇NO₃S₂
Molecular Weight:371.481
Hs Code.:
DSSTox Substance ID:DTXSID601181136
Nikkaji Number:J882.813J

Synonyms:DTXSID601181136;4-Methyl-N-(oxidodiphenyl-lambda4-sulfanylidene)benzenesulfonamide;38764-58-8

Suppliers and Price of 4-Methyl-N-(oxidodiphenyl-lambda4-sulfanylidene)benzenesulfonamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 4-Methyl-N-(oxidodiphenyl-lambda4-sulfanylidene)benzenesulfonamide

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:371.06498575
Heavy Atom Count:25
Complexity:615

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N=S(=O)(C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 4-Methyl-N-(oxidodiphenyl-lambda4-sulfanylidene)benzenesulfonamide

There total 13 articles about 4-Methyl-N-(oxidodiphenyl-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: 100.0%

: 13150-76-0
N-[(4-methylphenyl)sulfonyl]-S,S-diphenyl-sulfilimine

: 38764-58-8
4-methyl-N-(oxodiphenyl-λ⁶-sulfaneylidene)benzene sulfonamide

Guidance literature:: With sodium hypochlorite; tetrabutyl-ammonium chloride; In dichloromethane; ethyl acetate; Product distribution; Ambient temperature;
DOI:10.1016/S0040-4039(01)82045-1