[(Cyclohex-3-en-1-yl)oxy](trimethyl)silane

Base Information

Chemical Name:[(Cyclohex-3-en-1-yl)oxy](trimethyl)silane
CAS No.:66957-17-3
Molecular Formula:C₉H₁₈OSi
Molecular Weight:170.327
Hs Code.:
DSSTox Substance ID:DTXSID80540171
Nikkaji Number:J1.086.738J

Synonyms:[(Cyclohex-3-en-1-yl)oxy](trimethyl)silane;66957-17-3;DTXSID80540171

Suppliers and Price of [(Cyclohex-3-en-1-yl)oxy](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 [(Cyclohex-3-en-1-yl)oxy](trimethyl)silane

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:170.112691728
Heavy Atom Count:11
Complexity:146

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)OC1CCC=CC1

Technology Process of [(Cyclohex-3-en-1-yl)oxy](trimethyl)silane

There total 3 articles about [(Cyclohex-3-en-1-yl)oxy](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:

: 285-52-9
1,4-cyclohexadiene diepoxide

: 66957-17-3
4-(trimethylsilyloxy)cyclohex-1-ene

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / LiAlH₄

2: pyridine

With pyridine; lithium aluminium tetrahydride;
DOI:10.1021/ja00312a030

Reference yield:

: 1165952-92-0
cyclohexa-1,4-diene

: 66957-17-3
4-(trimethylsilyloxy)cyclohex-1-ene

Guidance literature:: Multi-step reaction with 3 steps

1: 35 percent / m-chloroperbenzoic acid

2: 73 percent / LiAlH₄

3: pyridine

With pyridine; lithium aluminium tetrahydride; 3-chloro-benzenecarboperoxoic acid;
DOI:10.1021/ja00312a030