[1-(Benzenesulfonyl)ethenyl](trimethyl)silane

Base Information

Chemical Name:[1-(Benzenesulfonyl)ethenyl](trimethyl)silane
CAS No.:69627-08-3
Molecular Formula:C11H16O2SSi
Molecular Weight:240.398
Hs Code.:
DSSTox Substance ID:DTXSID40497970
Nikkaji Number:J314.933A
Wikidata:Q82347753

Synonyms:[1-(Benzenesulfonyl)ethenyl](trimethyl)silane;69627-08-3;DTXSID40497970;1-phenylsulfonyl-1-(trimethylsilyl)ethylene

Suppliers and Price of [1-(Benzenesulfonyl)ethenyl](trimethyl)silane

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 1 raw suppliers

Chemical Property of [1-(Benzenesulfonyl)ethenyl](trimethyl)silane

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:240.06402746
Heavy Atom Count:15
Complexity:327

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)C(=C)S(=O)(=O)C1=CC=CC=C1

Technology Process of [1-(Benzenesulfonyl)ethenyl](trimethyl)silane

There total 4 articles about [1-(Benzenesulfonyl)ethenyl](trimethyl)silane 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: 96.0%

: 62762-20-3
1-phenylthio-1-trimethylsilylethene

: 69627-08-3
1-(phenylsulfonyl)-1-(trimethylsilyl)ethene

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid;
DOI:10.1248/cpb.38.902

Reference yield:

: 5535-49-9
2-Chloroethyl phenyl sulfide

: 69627-08-3
1-(phenylsulfonyl)-1-(trimethylsilyl)ethene

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / NaOH

2: 89 percent / LDA / tetrahydrofuran; hexane

3: 94 percent / aq. H₂O₂; glacial AcOH / 13 h / 20 - 30 °C

With sodium hydroxide; dihydrogen peroxide; acetic acid; lithium diisopropyl amide; In tetrahydrofuran; hexane;
DOI:10.1023/A:1021624329438

Reference yield:

: 108-98-5
thiophenol

: 69627-08-3
1-(phenylsulfonyl)-1-(trimethylsilyl)ethene

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / NaOH

2: 87 percent / NaOH

3: 89 percent / LDA / tetrahydrofuran; hexane

4: 94 percent / aq. H₂O₂; glacial AcOH / 13 h / 20 - 30 °C

With sodium hydroxide; dihydrogen peroxide; acetic acid; lithium diisopropyl amide; In tetrahydrofuran; hexane;
DOI:10.1023/A:1021624329438