1-phenyl-2-triethylsiloxyethene

Base Information

Chemical Name:1-phenyl-2-triethylsiloxyethene
CAS No.:56892-44-5
Molecular Formula:C₁₄H₂₂OSi
Molecular Weight:234.414
Hs Code.:

Synonyms:

Suppliers and Price of 1-phenyl-2-triethylsiloxyethene

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 0 raw suppliers

Chemical Property of 1-phenyl-2-triethylsiloxyethene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-phenyl-2-triethylsiloxyethene

There total 2 articles about 1-phenyl-2-triethylsiloxyethene 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:

: 96-09-3
styrene oxide

: 617-86-7
triethylsilane

: 56892-44-5,56892-48-9
1-phenyl-2-triethylsiloxyethene

: 14629-62-0
1-(triethylsiloxy)-2-phenylethane

Guidance literature:: With dicobalt octacarbonyl; Yield given. Yields of byproduct given;
DOI:10.1016/S0040-4039(00)98222-4

Reference yield:

: 994-30-9
triethylsilyl chloride

: 122-78-1
phenylacetaldehyde

: 56892-44-5,56892-48-9
1-phenyl-2-triethylsiloxyethene

Guidance literature:: With triethylamine; zinc(II) chloride;
DOI:10.1016/S0022-328X(00)94004-X

Reference yield:

: 56892-44-5,56892-48-9
1-phenyl-2-triethylsiloxyethene

: 162356-90-3
N-(tert-butoxycarbonyl)-2-bromobenzylamine

: C₂₀H₂₃NO₃

Guidance literature:: With 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate; tributyltin fluoride; cesium fluoride; In toluene; at 100 ℃; for 2h; regioselective reaction;
DOI:10.1021/acs.orglett.7b03776