2-Ethylhex-2-enol

Base Information

Chemical Name:2-Ethylhex-2-enol
CAS No.:38384-38-2
Molecular Formula:C8H16O
Molecular Weight:128.214
Hs Code.:
European Community (EC) Number:256-675-9
DSSTox Substance ID:DTXSID60880820
Nikkaji Number:J133.053E
Wikidata:Q82862208
Mol file:38384-38-2.mol

Synonyms:2-Ethylhex-2-enol;50639-00-4;2-ETHYL-2-HEXEN-1-OL;(E)-2-ethylhex-2-en-1-ol;2-Hexen-1-ol, 2-ethyl-;EINECS 256-675-9;2-Hexen-1-ol, 2-ethyl-, (E)-;38384-38-2;e-2-ethyl-2-hexenol;cis-2-Ethyl-2-hexen-1-ol;SCHEMBL1065703;DTXSID60880820;JSRFYJBJQPGAAA-SOFGYWHQSA-N;(2Z)-2-Ethyl-2-hexen-1-ol #;AKOS006346008;BS-53332;E77047

Suppliers and Price of 2-Ethylhex-2-enol

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 3 raw suppliers

Chemical Property of 2-Ethylhex-2-enol

Chemical Property:

PSA：20.23000
LogP:2.11520
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:128.120115130
Heavy Atom Count:9
Complexity:84.6

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCC=C(CC)CO
Isomeric SMILES:CCC/C=C(\CC)/CO

Technology Process of 2-Ethylhex-2-enol

There total 6 articles about 2-Ethylhex-2-enol 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:

: 645-62-5
2-ethylhexenal

: 38384-38-2
2-ethyl-hex-2-en-1-ol

: 104-76-7
2-Ethylhexyl alcohol

: 38384-39-3
(Z)-2-Ethylhex-2-en-1-ol

Guidance literature:: With bis(triphenylphosphine)copper(I) nitrate; hydrogen; 1,4-di(diphenylphosphino)-butane; sodium hydroxide; In ethanol; at 50 ℃; for 16h; under 37503.8 Torr; optical yield given as %de; chemoselective reaction; Autoclave; Inert atmosphere;
DOI:10.1055/s-0028-1216726