[(1E)-2-(Trifluorosilyl)ethenyl]benzene

Base Information

Chemical Name:[(1E)-2-(Trifluorosilyl)ethenyl]benzene
CAS No.:81501-26-0
Molecular Formula:C8H7F3Si
Molecular Weight:188.224
Hs Code.:
DSSTox Substance ID:DTXSID101278623
Nikkaji Number:J397.961J,J323.671D

Synonyms:SCHEMBL3162837;DTXSID101278623;[(1E)-2-(Trifluorosilyl)ethenyl]benzene;81501-26-0

Suppliers and Price of [(1E)-2-(Trifluorosilyl)ethenyl]benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of [(1E)-2-(Trifluorosilyl)ethenyl]benzene

Chemical Property:

PSA：0.00000
LogP:3.08640
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:188.02691124
Heavy Atom Count:12
Complexity:156

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=C[Si](F)(F)F
Isomeric SMILES:C1=CC=C(C=C1)/C=C/[Si](F)(F)F

Technology Process of [(1E)-2-(Trifluorosilyl)ethenyl]benzene

There total 3 articles about [(1E)-2-(Trifluorosilyl)ethenyl]benzene 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: 73.0%

: 3412-59-7
(E)-1-phenyl-2-trichlorosilylethene

: 81501-26-0
(E)-β-(trifluorosilyl)styrene

Guidance literature:: With copper (II)-fluoride; In diethyl ether; for 1h;
DOI:10.1016/0022-328X(83)85112-2

Reference yield:

: 536-74-3
phenylacetylene

: 81501-26-0
(E)-β-(trifluorosilyl)styrene

Guidance literature:: With dihydrogen hexachloroplatinate; copper (II)-fluoride; trichlorosilane; Multistep reaction; 1.) THF, reflux, 4 h;
DOI:10.1016/S0040-4020(97)00043-4

Reference yield:

: 536-74-3
phenylacetylene

: 81501-26-0
(E)-β-(trifluorosilyl)styrene

Guidance literature:: Multi-step reaction with 2 steps

1: H₂PtCl₆, SiCl₄

2: ZnF₂*2H₂O

With dihydrogen hexachloroplatinate; tetrachlorosilane; zinc(II) fluoride;
DOI:10.1039/c39890000957