[1-(Benzenesulfonyl)but-3-en-2-yl](trimethyl)silane

Base Information

Chemical Name:[1-(Benzenesulfonyl)but-3-en-2-yl](trimethyl)silane
CAS No.:89333-86-8
Molecular Formula:C₁₃H₂₀O₂SSi
Molecular Weight:268.452
Hs Code.:
DSSTox Substance ID:DTXSID90524720

Synonyms:89333-86-8;[1-(Benzenesulfonyl)but-3-en-2-yl](trimethyl)silane;DTXSID90524720

Suppliers and Price of [1-(Benzenesulfonyl)but-3-en-2-yl](trimethyl)silane

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of [1-(Benzenesulfonyl)but-3-en-2-yl](trimethyl)silane

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:268.09532758
Heavy Atom Count:17
Complexity:343

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[Si](C)(C)C(CS(=O)(=O)C1=CC=CC=C1)C=C

Technology Process of [1-(Benzenesulfonyl)but-3-en-2-yl](trimethyl)silane

There total 4 articles about [1-(Benzenesulfonyl)but-3-en-2-yl](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:

: 59431-14-0
(methylsulfanyl)methyl phenyl sulfone

: 89333-86-8
(1-Benzenesulfonylmethyl-allyl)-trimethyl-silane

Guidance literature:: Multi-step reaction with 4 steps

1: 66 percent / BuLi / tetrahydrofuran / -78 - 25 °C

2: m-CPBA / CH₂Cl₂ / 0 °C

3: CCl₄; methanol

4: 2.) Bu₃SnCH₂I, PhLi / 1.) THF, -78 deg C, 2.6 h; 2.) THF, -20 deg C, 0.3 h

With n-butyllithium; tri-n-butylstannylmethyl iodide; phenyllithium; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane;

Reference yield:

: 89333-90-4
(2-Benzenesulfonyl-2-methylsulfanyl-ethyl)-trimethyl-silane

: 89333-86-8
(1-Benzenesulfonylmethyl-allyl)-trimethyl-silane

Guidance literature:: Multi-step reaction with 3 steps

1: m-CPBA / CH₂Cl₂ / 0 °C

2: CCl₄; methanol

3: 2.) Bu₃SnCH₂I, PhLi / 1.) THF, -78 deg C, 2.6 h; 2.) THF, -20 deg C, 0.3 h

With tri-n-butylstannylmethyl iodide; phenyllithium; 3-chloro-benzenecarboperoxoic acid; In methanol; tetrachloromethane; dichloromethane;

Reference yield:

: 344437-67-8
(2-Benzenesulfonyl-2-methanesulfinyl-ethyl)-trimethyl-silane

: 89333-86-8
(1-Benzenesulfonylmethyl-allyl)-trimethyl-silane

Guidance literature:: Multi-step reaction with 2 steps

1: CCl₄; methanol

2: 2.) Bu₃SnCH₂I, PhLi / 1.) THF, -78 deg C, 2.6 h; 2.) THF, -20 deg C, 0.3 h

With tri-n-butylstannylmethyl iodide; phenyllithium; In methanol; tetrachloromethane;