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(Perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate

Base Information
  • Chemical Name:(Perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate
  • CAS No.:77758-79-3
  • Molecular Formula:C10H5F10IO3S
  • Molecular Weight:522.1
  • Hs Code.:2904909090
  • European Community (EC) Number:679-830-6
  • DSSTox Substance ID:DTXSID70375111
  • Mol file:77758-79-3.mol
(Perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate

Synonyms:77758-79-3;(perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate;(Perfluoro-n-propyl)phenyliodonium trifluoro-methanesulfonate;(Perfluoropropyl)phenyliodonium Trifluoromethanesulfonate;1,1,2,2,3,3,3-heptafluoropropyl(phenyl)iodanium;trifluoromethanesulfonate;1,1,2,2,3,3,3-heptafluoropropyl(phenyl)iodonium;(perfluoropropyl)(phenyl)iodonium trifluoromethanesulfonate;(heptafluoropropyl)(phenyl)iodanium trifluoromethanesulfonate;SCHEMBL3030270;DTXSID70375111;AKOS015853111;CS-0455747;FT-0641654;P1082;T72933;A839183;(Heptafluoropropyl)phenyliodonium Trifluoromethanesulfonate;(perfluoro-n-propyl)phenyliodonium trifluoromethanesufonate;1,1,2,2,3,3,3-heptakis(fluoranyl)propyl-phenyl-iodanium;tris(fluoranyl)methanesulfonate

Suppliers and Price of (Perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate
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
  • TRC
  • (Perfluoropropyl)phenyliodonium Trifluoromethanesulfonate
  • 10mg
  • $ 45.00
  • TCI Chemical
  • (Perfluoropropyl)phenyliodonium Trifluoromethanesulfonate >97.0%(T)
  • 1g
  • $ 286.00
  • Matrix Scientific
  • (Perfluoro-n-propyl)phenyliodonium trifluoro-methanesulfonate
  • 500mg
  • $ 125.00
  • Apolloscientific
  • (Perfluoro-N-propyl)phenyliodoniumtrifluoromethanesulfonate 97%
  • 1g
  • $ 245.00
  • American Custom Chemicals Corporation
  • (PERFLUORO-N-PROPYL)PHENYLIODONIUM TRIFLUOROMETHANESULFONATE 95.00%
  • 500MG
  • $ 292.95
  • AK Scientific
  • (Perfluoro-n-propyl)phenyliodoniumtrifluoro-methanesulfonate
  • 1g
  • $ 433.00
Total 19 raw suppliers
Chemical Property of (Perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate
Chemical Property:
  • PSA:65.58000 
  • LogP:1.86780 
  • Storage Temp.:Refrigerator 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:13
  • Rotatable Bond Count:3
  • Exact Mass:521.88444
  • Heavy Atom Count:25
  • Complexity:399
Purity/Quality:

97% *data from raw suppliers

(Perfluoropropyl)phenyliodonium Trifluoromethanesulfonate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)[I+]C(C(C(F)(F)F)(F)F)(F)F.C(F)(F)(F)S(=O)(=O)[O-]
  • Uses (Perfluoropropyl)phenyliodonium Trifluoromethanesulfonate (cas# 77758-79-3) is a useful building block used for perfluoroalkylations of carbanions and carbonyl compoiunds. Its electrochemical reduction has also been studied n the presence of sodium p-chlorophenylsulfinate, undergoing an ion-radical chain mechanism.
Technology Process of (Perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate

There total 1 articles about (Perfluoro-n-propyl)phenyliodonium trifluoromethanesulfonate 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:
Guidance literature:
With copper(l) iodide; In 1,2-dichloro-ethane; for 15h; stereoselective reaction; Inert atmosphere; Schlenk technique; Heating; Sealed tube;
DOI:10.1021/acs.orglett.7b01215
Guidance literature:
With copper(l) iodide; In 1,2-dichloro-ethane; for 15h; stereoselective reaction; Inert atmosphere; Schlenk technique; Heating; Sealed tube;
DOI:10.1021/acs.orglett.7b01215
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