Ethyl 4,7-octadienoate

Base Information

Chemical Name:Ethyl 4,7-octadienoate
CAS No.:69925-33-3
Molecular Formula:C₁₀H₁₆O₂
Molecular Weight:168.236
Hs Code.:
European Community (EC) Number:276-569-6
DSSTox Substance ID:DTXSID0072560
Nikkaji Number:J299.085G
Wikidata:Q76304630
Metabolomics Workbench ID:44710
Mol file:69925-33-3.mol

Synonyms:Ethyl 4,7-octadienoate;Ethyl (4Z)-4,7-octadienoate;ethyl (4E)-octa-4,7-dienoate;4,7-Octadienoic acid, ethyl ester;72276-09-6;EINECS 276-569-6;ethyl trans-4,7-octadienoate;SCHEMBL3504878;DTXSID0072560;SCHEMBL11123104;4,7-Octadienoic acid ethyl ester;CHEBI:180843;LMFA07010846;Ethyl ester(Z)-4,7-Octadienoic acid

Suppliers and Price of Ethyl 4,7-octadienoate

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 4 raw suppliers

Chemical Property of Ethyl 4,7-octadienoate

Chemical Property:

Vapor Pressure:0.258mmHg at 25°C
Boiling Point:204.8°C at 760 mmHg
Flash Point:73.2°C
PSA：26.30000
Density:0.905g/cm³
LogP:2.46200
XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:168.115029749
Heavy Atom Count:12
Complexity:159

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:CCOC(=O)CCC=CCC=C
Isomeric SMILES:CCOC(=O)CC/C=C/CC=C

Technology Process of Ethyl 4,7-octadienoate

There total 8 articles about Ethyl 4,7-octadienoate 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: 90.0%

: 81439-12-5
2-carbethoxy-4(Z),7-octadienoic acid

: 69925-33-3
ethyl (Z)-4,7-octadienoate

Guidance literature:: In N,N,N,N,N,N-hexamethylphosphoric triamide; at 180 ℃; for 3h;

Reference yield:

: 2749-86-2
hex-5-en-2-yn-1-ol

: 69925-33-3
ethyl (Z)-4,7-octadienoate

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / H₂ / Lindlar's catalyst, quinoline / hexane

2: 90 percent / PBr₃, pyridine / diethyl ether / 1) overnight, 2) reflux, 2 h

3: 1) sodium / 1) benzene, DMF, 2) benzene, reflux, 16 h

4: 60 percent / 10percent sodium hydroxide / methanol / 24 h

5: 90 percent / hexamethylphosphoric acid triamide / 3 h / 180 °C

With pyridine; sodium hydroxide; hydrogen; sodium; phosphorus tribromide; quinoline; Lindlar's catalyst; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; hexane;

Reference yield:

: 56879-14-2
ethyl (Z)-8-oxo-4-octenoate

: 69925-33-3
ethyl (Z)-4,7-octadienoate

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄ / ethanol

2: (i) Ac₂O, Py, (ii) (pyrolysis)

With sodium tetrahydroborate; In ethanol;
DOI:10.1002/hlca.19790620120