2,5,8,11-Tetraoxatetradec-13-ene

Base Information

Chemical Name:2,5,8,11-Tetraoxatetradec-13-ene
CAS No.:19685-21-3
Molecular Formula:C10H20O4
Molecular Weight:204.266
Hs Code.:
European Community (EC) Number:243-224-6
DSSTox Substance ID:DTXSID2066515
Nikkaji Number:J225.249J
Wikidata:Q81993098
Mol file:19685-21-3.mol

Synonyms:2,5,8,11-Tetraoxatetradec-13-ene;19685-21-3;3-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]prop-1-ene;Allyloxymethoxytriglycol;EINECS 243-224-6;Tetraoxatetradec-13-ene;YSZC668;SCHEMBL148189;DTXSID2066515;MFCD00080393;triethylene glycol allyl methyl ether;triethylene glycol methyl allyl ether;Allyl methoxy triethylene glycol ether;2,5,8,11-Tetraoxa-13-tetradecene;AKOS028110930;AS-68278;CS-0047709;T3914;A901434

Suppliers and Price of 2,5,8,11-Tetraoxatetradec-13-ene

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

Chem-Impex
2,5,8,11-Tetraoxatetradec-13-ene,97%(GC) 97%(GC)
100G
$ 285.60

Chem-Impex
2,5,8,11-Tetraoxatetradec-13-ene,97%(GC) 97%(GC)
25G
$ 85.12

Total 23 raw suppliers

Chemical Property of 2,5,8,11-Tetraoxatetradec-13-ene

Chemical Property:

Vapor Pressure:0.0424mmHg at 25°C
Melting Point:<0°C
Boiling Point:246.5°Cat760mmHg
Flash Point:80.8°C
PSA：36.92000
Density:0.953g/cm³
LogP:0.86860
XLogP3:0.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:11
Exact Mass:204.13615911
Heavy Atom Count:14
Complexity:117

Purity/Quality:

99.9% ^*data from raw suppliers

2,5,8,11-Tetraoxatetradec-13-ene,97%(GC) 97%(GC) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COCCOCCOCCOCC=C

Technology Process of 2,5,8,11-Tetraoxatetradec-13-ene

There total 3 articles about 2,5,8,11-Tetraoxatetradec-13-ene 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: 97.0%

: 112-35-6,95507-80-5
triethylene glucol monomethyl ether

: 106-95-6
allyl bromide

: 19685-21-3,27252-80-8
allyloxytri(ethylene glycol) monomethyl ether

Guidance literature:: triethylene glucol monomethyl ether; With sodium hydride; In tetrahydrofuran; mineral oil; at 0 ℃; for 0.5h; Inert atmosphere;

allyl bromide; In tetrahydrofuran; mineral oil; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1002/pola.28924

Reference yield: 65.0%

: 112-35-6,95507-80-5
triethylene glucol monomethyl ether

: 18854-48-3,27252-80-8
monoethylene glycol methyl allyl ether

: 19685-21-3,27252-80-8
allyloxytri(ethylene glycol) monomethyl ether

Guidance literature:: In ethyl acetate; toluene;

Reference yield: 60.0%

: 112-35-6,95507-80-5
triethylene glucol monomethyl ether

: 107-05-1
3-chloroprop-1-ene

: 19685-21-3,27252-80-8
allyloxytri(ethylene glycol) monomethyl ether

Guidance literature:: triethylene glucol monomethyl ether; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 0.0833333h; Inert atmosphere;

3-chloroprop-1-ene; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 0.666667h;
DOI:10.1021/ja8026168