Tributyl(trifluoroethenyl)stannane

Base Information

Chemical Name:Tributyl(trifluoroethenyl)stannane
CAS No.:1426-65-9
Molecular Formula:C14H27F3Sn
Molecular Weight:371.074
Hs Code.:2931900090
European Community (EC) Number:890-035-5
DSSTox Substance ID:DTXSID50451083
Mol file:1426-65-9.mol

Synonyms:1426-65-9;Tributyl(trifluoroethenyl)stannane;1,2,2-Trifluoroethenyl-tributyltin;trifluorovinyltributyltin;TRIBUTYL(1,2,2-TRIFLUOROETHENYL)STANNANE;SCHEMBL7792024;DTXSID50451083;PWGPFNBKVNMDLK-UHFFFAOYSA-N;EN300-27737409

Suppliers and Price of Tributyl(trifluoroethenyl)stannane

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

Total 11 raw suppliers

Chemical Property of Tributyl(trifluoroethenyl)stannane

Chemical Property:

Refractive Index:1.4530 (589.3 nm 20℃)
Boiling Point:91-92℃ (0.5 Torr)
Flash Point:122.9±30.1℃
PSA：0.00000
LogP:5.44260
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:10
Exact Mass:372.108688
Heavy Atom Count:18
Complexity:226

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC[Sn](CCCC)(CCCC)C(=C(F)F)F
General Description 1,2,2-Trifluoroethenyl-tributyltin is an organotin compound characterized by a trifluoroethenyl group bonded to a tributyltin moiety. It is used in organic synthesis, particularly in reactions involving the transfer of the trifluoroethenyl group, such as cross-coupling or Stille-type reactions. 1,2,2-Trifluoroethenyl-tributyltin is notable for its reactivity in forming carbon-carbon bonds with electrophiles, making it valuable in the preparation of fluorinated organic molecules. Due to the presence of fluorine atoms, it may confer enhanced stability or unique electronic properties to the resulting products. However, like other organotin compounds, it requires careful handling due to potential toxicity.

Technology Process of Tributyl(trifluoroethenyl)stannane

There total 8 articles about Tributyl(trifluoroethenyl)stannane 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: 63.0%

: 758-93-0
perfluorvinylmagnesium bromide

: 1426-65-9
1,2,2-trifluorovinyl tri-n-butylstannane

Guidance literature:: With tri-n-butyl halogeno stannane; In tetrahydrofuran; reaction at 45 - 50°C, 15 hours;;
DOI:10.1021/ja01532a063 DOI:10.1021/ja01509a005