1-Ethenoxy-1-ethenylcyclohexane

Base Information

Chemical Name:1-Ethenoxy-1-ethenylcyclohexane
CAS No.:88739-01-9
Molecular Formula:C10H16O
Molecular Weight:152.236
Hs Code.:
DSSTox Substance ID:DTXSID90574947
Wikidata:Q82464145

Synonyms:1-ethenoxy-1-ethenylcyclohexane;88739-01-9;1-vinyl-1-(vinyloxy)cyclohexane;DTXSID90574947;1-Ethenyl-1-(ethenyloxy)cyclohexane;AKOS015906353

Suppliers and Price of 1-Ethenoxy-1-ethenylcyclohexane

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-Ethenoxy-1-ethenylcyclohexane

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:152.120115130
Heavy Atom Count:11
Complexity:143

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=CC1(CCCCC1)OC=C

Technology Process of 1-Ethenoxy-1-ethenylcyclohexane

There total 2 articles about 1-Ethenoxy-1-ethenylcyclohexane 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: 77.0%

: 88738-95-8
2-bromoethyl 1-(1-bromoethyl)cyclohexyl ether

: 88739-01-9
vinyl 1-vinylcyclohexanyl ether

Guidance literature:: With potassium tert-butylate; In dimethyl sulfoxide; Ambient temperature;
DOI:10.1055/s-1993-25872

Reference yield:

: 1003-64-1
ethylidenecyclohexane

: 88739-01-9
vinyl 1-vinylcyclohexanyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / Br₂ / CH₂Cl₂ / 0.5 h / -80 °C

2: 77 percent / t-BuOK / dimethylsulfoxide / Ambient temperature

With potassium tert-butylate; bromine; In dichloromethane; dimethyl sulfoxide;
DOI:10.1055/s-1993-25872