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[(1E)-cycloocten-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate

Base Information
  • Chemical Name:[(1E)-cycloocten-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
  • CAS No.:36839-96-0
  • Molecular Formula:C12H13F9O3S
  • Molecular Weight:408.2804
  • Hs Code.:
  • NSC Number:263695
  • DSSTox Substance ID:DTXSID50420375
  • Wikidata:Q82231634
[(1E)-cycloocten-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate

Synonyms:NSC263695;36839-96-0;DTXSID50420375;NSC-263695;(1E)-1-Cycloocten-1-yl 1,1,2,2,3,3,4,4,4-nonafluoro-1-butanesulfonate

Suppliers and Price of [(1E)-cycloocten-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 2 raw suppliers
Chemical Property of [(1E)-cycloocten-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
Chemical Property:
  • Vapor Pressure:0.000838mmHg at 25°C 
  • Boiling Point:314.9°C at 760 mmHg 
  • Flash Point:144.2°C 
  • Density:1.48g/cm3 
  • XLogP3:5.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:12
  • Rotatable Bond Count:5
  • Exact Mass:408.04416890
  • Heavy Atom Count:25
  • Complexity:602
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCCC(=CCC1)OS(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F
  • Isomeric SMILES:C1CCC/C(=C\CC1)/OS(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F
Technology Process of [(1E)-cycloocten-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate

There total 3 articles about [(1E)-cycloocten-1-yl] 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate 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:
In dichloromethane; cooled down solution of (n-C4F9SO2)2O to -15°C, then stirring for 2 days at room temp.;
Guidance literature:
In 1,2-dimethoxyethane; the Na salt of the ketone is prepared in the react. mixture from NaH and the corresponding ketone, at 0°C C4F9SO2F is added, stirring 1 h, refluxed at 50-60°C, 15 h;
Guidance literature:
With sodium carbonate; In dichloromethane;
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