(E)-8-Dodecen-1-yl acetate

Base Information

Chemical Name:(E)-8-Dodecen-1-yl acetate
CAS No.:38363-29-0
Molecular Formula:C14H26 O2
Molecular Weight:226.359
Hs Code.:
European Community (EC) Number:253-904-4
UNII:0JM5ZAB30X
DSSTox Substance ID:DTXSID5035294
Nikkaji Number:J688B,J260.758A
Wikidata:Q27236867
Metabolomics Workbench ID:3872
Mol file:38363-29-0.mol

Synonyms:(E)-dodec-8-en-1-yl acetate

Suppliers and Price of (E)-8-Dodecen-1-yl 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

TRC
(8E)-DodecenylAcetate
50mg
$ 75.00

TRC
(8E)-DodecenylAcetate
500mg
$ 655.00

American Custom Chemicals Corporation
(E)-8-DODECEN-1-YL ACETATE 98.00%
100G
$ 2836.68

AHH
(E)-8-Dodecen-1-ylacetate 98%
100g
$ 360.00

Activate Scientific
(E)-8-Dodecen-1-ylacetate 90%
1 g
$ 838.00

Activate Scientific
(E)-8-Dodecen-1-ylacetate 90%
100 mg
$ 248.00

Total 46 raw suppliers

Chemical Property of (E)-8-Dodecen-1-yl acetate

Chemical Property:

Vapor Pressure:0.00114mmHg at 25°C
Refractive Index:1.448
Boiling Point:300.1°Cat760mmHg
Flash Point:96.5°C
PSA：26.30000
Density:0.881g/cm³
LogP:4.24640
Storage Temp.:-20°C
Solubility.:Chloroform (Slightly), Dichloromethane (Slightly)
XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:11
Exact Mass:226.193280068
Heavy Atom Count:16
Complexity:185

Purity/Quality:

90% ^*data from raw suppliers

(8E)-DodecenylAcetate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC=CCCCCCCCOC(=O)C
Isomeric SMILES:CCC/C=C/CCCCCCCOC(=O)C
Uses (8E)-Dodecenyl Acetate functions as pheromone of green budworm moth.

Technology Process of (E)-8-Dodecen-1-yl acetate

There total 30 articles about (E)-8-Dodecen-1-yl 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: 98.0%

: 42513-42-8
E₈,E₁₀-dodecadien-1-ol

: 75-36-5
acetyl chloride

: 38363-29-0
(E)-8-dodecenyl acetate

Guidance literature:: With pyridine; In dichloromethane; for 2h;
DOI:10.1023/A:1012242904220

Reference yield: 95.0%

: 42513-42-8
E₈,E₁₀-dodecadien-1-ol

: 108-24-7
acetic anhydride

: 38363-29-0
(E)-8-dodecenyl acetate

Guidance literature:: With pyridine; at -25 ℃; for 24h;
DOI:10.1007/BF00574216

Reference yield:

: 64604-68-8
1-(2-tetrahydropyranyloxy)dodec-8-ene

: 75-36-5
acetyl chloride

: 28079-04-1
(Z)-8-dodecen-1-yl acetate

: 38363-29-0
(E)-8-dodecenyl acetate

Guidance literature:: 1-(2-tetrahydropyranyloxy)dodec-8-ene; With nickel dihydroxide; hydrogen; In methanol; Cooling with ice;

acetyl chloride; In n-heptane; water; at 40 ℃; Solvent; Reagent/catalyst; Temperature; Overall yield = 16.1 g;