(4-Iodophenyl)diphenylsulfonium triflate

Base Information

Chemical Name:(4-Iodophenyl)diphenylsulfonium triflate
CAS No.:255056-46-3
Molecular Formula:C20H16F3IO3S2
Molecular Weight:538.34
Hs Code.:2930909899
European Community (EC) Number:622-012-0
DSSTox Substance ID:DTXSID40584137
Mol file:255056-46-3.mol

Synonyms:(4-Iodophenyl)diphenylsulfonium triflate;255056-46-3;(4-iodophenyl)-diphenylsulfanium;trifluoromethanesulfonate;Diphenyl(4-iodophenyl)sulphonium triflate;(4-Iodophenyl)diphenylsulfonium trifluoromethanesulfonate;SCHEMBL51548;DTXSID40584137;WHQDLCHSPLKATA-UHFFFAOYSA-N;MFCD02683574;(4-Iodophenyl)diphenylsulfoniumtrifluoromethanesulfonate;(4-Iodophenyl)(diphenyl)sulfanium trifluoromethanesulfonate

Suppliers and Price of (4-Iodophenyl)diphenylsulfonium triflate

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
(4-Iodophenyl)diphenylsulfonium triflate
1g
$ 103.00

Total 7 raw suppliers

Chemical Property of (4-Iodophenyl)diphenylsulfonium triflate

Chemical Property:

Melting Point:155-160 °C(lit.)
PSA：90.88000
LogP:6.51880
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:537.93812
Heavy Atom Count:28
Complexity:400

Purity/Quality:

99% ^*data from raw suppliers

(4-Iodophenyl)diphenylsulfonium triflate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC=C(C=C1)[S+](C2=CC=CC=C2)C3=CC=C(C=C3)I.C(F)(F)(F)S(=O)(=O)[O-]
Uses Cationic photoinitiator. Photoacid generator.

Technology Process of (4-Iodophenyl)diphenylsulfonium triflate

There total 1 articles about (4-Iodophenyl)diphenylsulfonium triflate 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:

Reference yield: 82.0%

: 255056-46-3
(4-iodophenyl)diphenylsulfonium triflate

Guidance literature:

Reference yield:

: 255056-46-3
(4-iodophenyl)diphenylsulfonium triflate

: 153750-28-8
1-[¹⁸F]fluoro-4-iodobenzene

Guidance literature:: (4-iodophenyl)diphenylsulfonium triflate; With [18F]fluoride ion, cyclotron produced, NCA; In methanol;

In Dimethyl ether; at 85 ℃; for 0.25h;
DOI:10.1039/c4ob01336k

Reference yield:

: 255056-46-3
(4-iodophenyl)diphenylsulfonium triflate

: [¹⁸F]pitavastatin

Guidance literature:: Multi-step reaction with 2 steps

1: F- / acetonitrile / 0.02 h / Microwave irradiation

2: caesium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / acetonitrile / 0.02 h / 100 °C / Microwave irradiation

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; In acetonitrile; 2: |Suzuki Coupling;
DOI:10.1039/c4ob01953a