ethyl (E)-3-cyclohexyloxyprop-2-enoate

Base Information

Chemical Name:ethyl (E)-3-cyclohexyloxyprop-2-enoate
CAS No.:7506-99-2
Molecular Formula:C₁₁H₁₈O₃
Molecular Weight:198.262
Hs Code.:
NSC Number:407863
DSSTox Substance ID:DTXSID40419713
Wikidata:Q82230879

Synonyms:7506-99-2;NSC407863;ethyl (E)-3-cyclohexyloxyprop-2-enoate;DTXSID40419713;NSC-407863;ethyl (2E)-3-(cyclohexyloxy)-2-propenoate

Suppliers and Price of ethyl (E)-3-cyclohexyloxyprop-2-enoate

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 2 raw suppliers

Chemical Property of ethyl (E)-3-cyclohexyloxyprop-2-enoate

Chemical Property:

Vapor Pressure:0.000979mmHg at 25°C
Boiling Point:302.6°C at 760 mmHg
Flash Point:123.1°C
Density:1.01g/cm³
XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:198.125594432
Heavy Atom Count:14
Complexity:193

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C=COC1CCCCC1
Isomeric SMILES:CCOC(=O)/C=C/OC1CCCCC1

Technology Process of ethyl (E)-3-cyclohexyloxyprop-2-enoate

There total 3 articles about ethyl (E)-3-cyclohexyloxyprop-2-enoate 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:

: 1001-26-9
ethyl 3-ethoxyacrylate

: 7506-99-2
3-cyclohexyloxy-acrylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NaHSO₄ / 80 - 90 °C

2: NaHSO₄

With sodium hydrogen sulfate;
DOI:10.1021/ja01176a041