Azobenzene-4,4'-disulfonamide

Base Information

Chemical Name:Azobenzene-4,4'-disulfonamide
CAS No.:4320-29-0
Molecular Formula:C₁₂H₁₂N₄O₄S₂
Molecular Weight:340.384
Hs Code.:
DSSTox Substance ID:DTXSID901302052
Nikkaji Number:J519.642F

Synonyms:Azobenzene-4,4'-disulfonamide;4320-29-0;Benzenesulfonamide, 4,4'-azobis-;DTXSID901302052

Suppliers and Price of Azobenzene-4,4'-disulfonamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Azobenzene-4,4'-disulfonamide

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:340.02999722
Heavy Atom Count:22
Complexity:536

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N=NC2=CC=C(C=C2)S(=O)(=O)N)S(=O)(=O)N

Technology Process of Azobenzene-4,4'-disulfonamide

There total 19 articles about Azobenzene-4,4'-disulfonamide 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: 80.0%

: 63-74-1
sulfanilamide

: 4320-29-0
Azobenzene-4,4'-disulphonamide

Guidance literature:: With sodium perborate; sodium molybdate tetrahydrate; In acetic acid; at 50 ℃; for 1h; Temperature; Kinetics; Thermodynamic data; Catalytic behavior;
DOI:10.1007/s11696-018-0599-z

Reference yield: 53.0%

: 6325-93-5
p-nitrobenzenesulfonamide

: 4320-29-0
Azobenzene-4,4'-disulphonamide

Guidance literature:: p-nitrobenzenesulfonamide; With indium(III) triflate; triethylsilane; In N,N-dimethyl-formamide; at 60 ℃; Inert atmosphere;

In N,N-dimethyl-formamide; for 5h; chemoselective reaction; Mechanism;
DOI:10.1016/j.tet.2014.01.048