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2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride

Base Information Edit
  • Chemical Name:2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride
  • CAS No.:125662-61-5
  • Molecular Formula:C7F6O3S
  • Molecular Weight:278.132
  • Hs Code.:
  • DSSTox Substance ID:DTXSID501207694
  • Mol file:125662-61-5.mol
2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride

Synonyms:SCHEMBL5274780;2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride;DTXSID501207694;125662-61-5

Suppliers and Price of 2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride
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
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Total 0 raw suppliers
Chemical Property of 2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride Edit
Chemical Property:
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:2
  • Exact Mass:277.94723400
  • Heavy Atom Count:17
  • Complexity:390
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1(=C(C(=C(C(=C1F)F)S(=O)(=O)F)F)F)C(=O)F
Technology Process of 2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride

There total 5 articles about 2,3,5,6-Tetrafluoro-4-(fluorosulfonyl)benzoyl fluoride 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 sulfur tetrafluoride; at 80 ℃; for 18h; Yield given;
DOI:10.1016/S0022-1139(00)80200-6
Guidance literature:
Multi-step reaction with 4 steps
1: aq. NaOH, NaHS / 2 h / 70 °C
2: 978 mg / 30percent H2O2, AcOH / 2 h / 70 °C
3: SOCl2, DMF / 6 h / Heating
4: SF4 / 18 h / 80 °C
With sodium hydroxide; sodium hydrogensulfide; thionyl chloride; sulfur tetrafluoride; dihydrogen peroxide; acetic acid; N,N-dimethyl-formamide;
DOI:10.1016/S0022-1139(00)80200-6
Guidance literature:
Multi-step reaction with 3 steps
1: 978 mg / 30percent H2O2, AcOH / 2 h / 70 °C
2: SOCl2, DMF / 6 h / Heating
3: SF4 / 18 h / 80 °C
With thionyl chloride; sulfur tetrafluoride; dihydrogen peroxide; acetic acid; N,N-dimethyl-formamide;
DOI:10.1016/S0022-1139(00)80200-6
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