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M-Nitrobenzenesulfonyl peroxide

Base Information Edit
  • Chemical Name:M-Nitrobenzenesulfonyl peroxide
  • CAS No.:6209-71-8
  • Molecular Formula:C12H8N2O10S2
  • Molecular Weight:404.335
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20557920
  • Wikidata:Q82439989
  • Mol file:6209-71-8.mol
M-Nitrobenzenesulfonyl peroxide

Synonyms:M-NITROBENZENESULFONYL PEROXIDE;6209-71-8;DTXSID20557920;1,1'-(Peroxydisulfonyl)bis(3-nitrobenzene)

Suppliers and Price of M-Nitrobenzenesulfonyl peroxide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of M-Nitrobenzenesulfonyl peroxide Edit
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:5
  • Exact Mass:403.96203680
  • Heavy Atom Count:26
  • Complexity:664
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC(=C1)S(=O)(=O)OOS(=O)(=O)C2=CC=CC(=C2)[N+](=O)[O-])[N+](=O)[O-]
Technology Process of M-Nitrobenzenesulfonyl peroxide

There total 1 articles about M-Nitrobenzenesulfonyl peroxide 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:
Guidance literature:
With dihydrogen peroxide; potassium carbonate; In ethanol; chloroform;
DOI:10.1021/jo00834a045
Guidance literature:
In chloroform; for 168h; Ambient temperature;
DOI:10.1021/jo00375a051
Guidance literature:
In ethyl acetate; at -78 ℃;
DOI:10.1021/ja00260a015
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