Silane, trimethyl[[1-(phenylthio)ethenyl]oxy]-

Base Information

Chemical Name:Silane, trimethyl[[1-(phenylthio)ethenyl]oxy]-
CAS No.:80675-54-3
Molecular Formula:C11H16OSSi
Molecular Weight:224.399
Hs Code.:
DSSTox Substance ID:DTXSID30466170
Nikkaji Number:J905.440E
Wikidata:Q82292666

Synonyms:Silane, trimethyl[[1-(phenylthio)ethenyl]oxy]-;80675-54-3;SCHEMBL8424511;DTXSID30466170;NOTYNGUSRPLVCS-UHFFFAOYSA-N;1-phenylthio-1-(trimethylsilyloxy)ethylene

Suppliers and Price of Silane, trimethyl[[1-(phenylthio)ethenyl]oxy]-

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
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price

Total 1 raw suppliers

Chemical Property of Silane, trimethyl[[1-(phenylthio)ethenyl]oxy]-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:224.06911284
Heavy Atom Count:14
Complexity:192

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[Si](C)(C)OC(=C)SC1=CC=CC=C1

Technology Process of Silane, trimethyl[[1-(phenylthio)ethenyl]oxy]-

There total 6 articles about Silane, trimethyl[[1-(phenylthio)ethenyl]oxy]- 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: 83.0%

: 75-77-4
chloro-trimethyl-silane

: 934-87-2
S-phenyl thioacetate

: 80675-54-3
((1-(phenylthio)vinyl)oxy)trimethylsilane

Guidance literature:: With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at 20 ℃; for 1.1h;
DOI:10.1246/cl.131095

Reference yield:

: 934-87-2
S-phenyl thioacetate

: 27607-77-8
trimethylsilyl trifluoromethanesulfonate

: 80675-54-3
((1-(phenylthio)vinyl)oxy)trimethylsilane

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1016/S0040-4020(00)00331-8

Reference yield:

: 63877-23-6
(trimethylsilyl)acetyl chloride

: 80675-54-3
((1-(phenylthio)vinyl)oxy)trimethylsilane

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / diisopropylethylamine / CH₂Cl₂ / -15 °C

2: TfOTMS / CDCl₃

With N-ethyl-N,N-diisopropylamine; trimethylsilyl trifluoromethanesulfonate; In chloroform-d1; dichloromethane;
DOI:10.1016/S0040-4039(00)89176-5