(Z)-8-DODECEN-1-YL ACETATE

Base Information

• Chemical Name: (Z)-8-DODECEN-1-YL ACETATE
• CAS No.: 28079-04-1
• Molecular Formula: C14H26O2
• Molecular Weight: 226.359
• Hs Code.: 2915390090
• European Community (EC) Number: 248-823-6
• UNII: 0MWD335OTN
• DSSTox Substance ID: DTXSID9035543
• Nikkaji Number: J4.090H
• Wikidata: Q27236972
• Metabolomics Workbench ID: 3890
• Mol file: 28079-04-1.mol

Synonyms:8-Dodecen-1-ol,acetate, (8Z)- (9CI);8-Dodecen-1-ol, acetate, (Z)- (8CI);(8Z)-Dodec-8-en-1-olacetate;(Z)-8-Dodecen-1-ol acetate;(Z)-8-Dodecen-1-yl acetate;(Z)-8-Dodecenyl acetate;Denacil;Funemone;GM;Orfamone;cis-8-Dodecen-1-yl acetate;8-Dodecen-1-ol,1-acetate, (8Z)-;

Chemical Property of (Z)-8-DODECEN-1-YL ACETATE

Chemical Property:

• Vapor Pressure: 0.00114mmHg at 25°C
• Refractive Index: 1.448
• Boiling Point: 300.1 °C at 760 mmHg
• Flash Point: 96.5 °C
• PSA: 26.30000
• Density: 0.881 g/cm³
• LogP: 4.24640
• Storage Temp.: 2-8°C
• Solubility.: DMSO (Slightly), Water (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:

93% ^*data from raw suppliers

GentamicinDeuterated(CComplex)PentaacetateSalt(Containsd0) ^*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
• General Description: (Z)-8-DODECEN-1-YL ACETATE is a sex pheromone component found in many Lepidoptera species, synthesized via a three-step process from cyclooctene. It is produced by the acetylation of (Z)-8-dodecen-1-ol, which is derived from the reduction of methyl (Z)-8-dodecenoate, itself obtained through ozonolysis and Wittig coupling. (Z)-8-DODECEN-1-YL ACETATE is structurally characterized by a (Z)-configured double bond at the 8-position and an acetate ester at the terminal carbon, playing a key role in insect communication.

Technology Process of (Z)-8-DODECEN-1-YL ACETATE

There total 76 articles about (Z)-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: 97.0%

1-Acetoxydodec-8-yne (26906-26-3) → (Z)-8-dodecen-1-yl acetate (28079-04-1)

Guidance literature:

With quinoline; hydrogen; Pd-BaSO₄; In methanol;

Reference yield: 95.0%

Δ8-dodecen-1-ol (153123-34-3) + acetic anhydride (108-24-7) → (Z)-8-dodecen-1-yl acetate (28079-04-1)

Guidance literature:

With pyridine; at 5 - 25 ℃; for 2h; Large scale;

Reference yield: 95.0%

(Z)-8-dodecenol (40642-40-8) + acetyl chloride (75-36-5) → (Z)-8-dodecen-1-yl acetate (28079-04-1)

Guidance literature:

In pyridine;

upstream raw materials:

(E)-8-dodecenyl acetate

(Z)-8-dodecenol

acetyl chloride

1-Acetoxydodec-8-yne