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2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite

Base Information
  • Chemical Name:2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite
  • CAS No.:78499-30-6
  • Molecular Formula:C7H3F13O2S
  • Molecular Weight:398.145
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30505795
2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite

Synonyms:78499-30-6;2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite;DTXSID30505795

Suppliers and Price of 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite
Chemical Property:
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:16
  • Rotatable Bond Count:8
  • Exact Mass:397.9646166
  • Heavy Atom Count:23
  • Complexity:448
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(C(C(C(C(C(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)OS(=O)F
Technology Process of 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite

There total 3 articles about 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl sulfurofluoridoite 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 (1,1,7-trihydrododecafluoroheptyloxy)difluorosulfonium tetrafluoroborate; In 1,1,2-Trichloro-1,2,2-trifluoroethane; 1.) -30 to -10 deg C, 1 h; 2.) to 30 deg C;
Guidance literature:
With (1,1,7-trihydrododecafluoroheptyloxy)difluorosulfonium hexafluoroantimonate; at -20 ℃; for 2h;
upstream raw materials:

trimethylsilyl acetate

acetic acid

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