(E,Z)-3,13-Octadecadienyl acetate

Base Information

Chemical Name:(E,Z)-3,13-Octadecadienyl acetate
CAS No.:57491-35-7
Molecular Formula:C20H36 O2
Molecular Weight:308.505
Hs Code.:
European Community (EC) Number:260-766-9
DSSTox Substance ID:DTXSID601017195
Metabolomics Workbench ID:4036
Mol file:57491-35-7.mol

Synonyms:57491-35-7;3Z,13E-Octadecadienyl acetate;(3Z,13E)-Octadeca-3,13-dienyl acetate;(Z,E)-3,13-Octadecadienyl acetate;EINECS 260-766-9;3,13-Octadecadien-1-ol, 1-acetate, (3Z,13E)-;(3Z,13E)-OCTADECA-3,13-DIEN-1-YL ACETATE;(E,Z)-3,13-Octadecadienyl acetate;e,z-3,13-octadecadienyl acetate;3,13-Octadecadien-1-ol, acetate, (Z,E)-;[(3Z,13E)-octadeca-3,13-dienyl] acetate;CHEBI:180342;VVJPJXKHBZNADP-NGLZPYLXSA-N;DTXSID601017195;LMFA07010391;Z,E-3,13-Octadecadien-1-ol acetate;(Z,E)-3,13-Octadecadien-1-ol acetate;(3Z,13E)-3,13-Octadecadienyl acetate #

Suppliers and Price of (E,Z)-3,13-Octadecadienyl acetate

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 (E,Z)-3,13-Octadecadienyl acetate

Chemical Property:

Vapor Pressure:2.67E-06mmHg at 25°C
Boiling Point:390.3°Cat760mmHg
Flash Point:97.6°C
PSA：26.30000
Density:0.882g/cm³
LogP:6.36300
XLogP3:7.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:16
Exact Mass:308.271530387
Heavy Atom Count:22
Complexity:292

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC=CCCCCCCCCC=CCCOC(=O)C
Isomeric SMILES:CCCC/C=C/CCCCCCCC/C=C\CCOC(=O)C

Technology Process of (E,Z)-3,13-Octadecadienyl acetate

There total 12 articles about (E,Z)-3,13-Octadecadienyl acetate 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:

: 928342-54-5
C₁₄H₂₇I

: 57491-35-7
3(Z),13(E)-octadecadien-1-yl acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran

1.2: tetrahydrofuran; hexamethylphosphoric acid triamide / 1 h / 20 °C

2.1: hydrogen / palladium on barium sulfate poisoned with quinoline / 1 h / 20 °C

3.1: p-toluenesulfonic acid / ethanol / 3 h / Heating

4.1: pyridine / 0.5 h / 20 °C

With pyridine; n-butyllithium; hydrogen; toluene-4-sulfonic acid; palladium on barium sulfate poisoned with quinoline; In tetrahydrofuran; ethanol;
DOI:10.1271/bbb.70.508

Reference yield:

: 50816-20-1
2-(8-bromooctyloxy)tetrahydropyran

: 57491-35-7
3(Z),13(E)-octadecadien-1-yl acetate

Guidance literature:: Multi-step reaction with 8 steps

1.1: n-butyllithium / tetrahydrofuran

1.2: tetrahydrofuran; hexamethylphosphoric acid triamide / 1 h / 20 °C

2.1: lithium; ethylamine / 1 h / -5 °C

3.1: p-toluenesulfonic acid / ethanol / 3 h / Heating

4.1: iodine; triphenylphosphine; imidazole / diethyl ether; acetonitrile / 1 h / 0 °C

5.1: n-butyllithium / tetrahydrofuran

5.2: tetrahydrofuran; hexamethylphosphoric acid triamide / 1 h / 20 °C

6.1: hydrogen / palladium on barium sulfate poisoned with quinoline / 1 h / 20 °C

7.1: p-toluenesulfonic acid / ethanol / 3 h / Heating

8.1: pyridine / 0.5 h / 20 °C

With pyridine; 1H-imidazole; n-butyllithium; hydrogen; iodine; lithium; toluene-4-sulfonic acid; ethylamine; triphenylphosphine; palladium on barium sulfate poisoned with quinoline; In tetrahydrofuran; diethyl ether; ethanol; acetonitrile; 2.1: Birch reduction;
DOI:10.1271/bbb.70.508

Reference yield:

: 629-41-4
1,8-Octanediol

: 57491-35-7
3(Z),13(E)-octadecadien-1-yl acetate

Guidance literature:: Multi-step reaction with 10 steps

1.1: HBr / toluene / 18 h / Heating

2.1: 3 h

3.1: n-butyllithium / tetrahydrofuran

3.2: tetrahydrofuran; hexamethylphosphoric acid triamide / 1 h / 20 °C

4.1: lithium; ethylamine / 1 h / -5 °C

5.1: p-toluenesulfonic acid / ethanol / 3 h / Heating

6.1: iodine; triphenylphosphine; imidazole / diethyl ether; acetonitrile / 1 h / 0 °C

7.1: n-butyllithium / tetrahydrofuran

7.2: tetrahydrofuran; hexamethylphosphoric acid triamide / 1 h / 20 °C

8.1: hydrogen / palladium on barium sulfate poisoned with quinoline / 1 h / 20 °C

9.1: p-toluenesulfonic acid / ethanol / 3 h / Heating

10.1: pyridine / 0.5 h / 20 °C

With pyridine; 1H-imidazole; n-butyllithium; hydrogen bromide; hydrogen; iodine; lithium; toluene-4-sulfonic acid; ethylamine; triphenylphosphine; palladium on barium sulfate poisoned with quinoline; In tetrahydrofuran; diethyl ether; ethanol; toluene; acetonitrile; 4.1: Birch reduction;
DOI:10.1271/bbb.70.508