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Phenyl 2,4-dinitrobenzenesulfonate

Base Information
  • Chemical Name:Phenyl 2,4-dinitrobenzenesulfonate
  • CAS No.:31283-98-4
  • Molecular Formula:C12H8N2O7S
  • Molecular Weight:324.271
  • Hs Code.:
  • European Community (EC) Number:660-593-2
  • Nikkaji Number:J3.663.176G
  • Mol file:31283-98-4.mol
Phenyl 2,4-dinitrobenzenesulfonate

Synonyms:phenyl 2,4-dinitrobenzenesulfonate;SCHEMBL20547997;AKOS024340873

Suppliers and Price of Phenyl 2,4-dinitrobenzenesulfonate
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
  • Packaging
  • price
  • Sigma-Aldrich
  • PHENYL 2,4-DINITROBENZENESULFONATE AldrichCPR
  • 1ea
  • $ 57.00
Total 1 raw suppliers
Chemical Property of Phenyl 2,4-dinitrobenzenesulfonate
Chemical Property:
  • PSA:143.39000 
  • LogP:4.39790 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:324.00522177
  • Heavy Atom Count:22
  • Complexity:513
Purity/Quality:

98%,99%, *data from raw suppliers

PHENYL 2,4-DINITROBENZENESULFONATE AldrichCPR *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)OS(=O)(=O)C2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]
Technology Process of Phenyl 2,4-dinitrobenzenesulfonate

There total 2 articles about Phenyl 2,4-dinitrobenzenesulfonate 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:
phenol; With triethylamine; In dichloromethane; at 0 ℃; for 1h; Inert atmosphere;
2,4-dinitrobenzenesulfonyl chloride; In dichloromethane; at 0 ℃; for 18h; Inert atmosphere;
DOI:10.1002/anie.201701188
Guidance literature:
In acetonitrile; at 25 ℃; for 2h; chemoselective reaction;
DOI:10.1039/d1ra03271b
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