(E)-9-Dodecenyl acetate

Base Information

• Chemical Name: (E)-9-Dodecenyl acetate
• CAS No.: 35148-19-7
• Molecular Formula: C14H26 O2
• Molecular Weight: 226.359
• Hs Code.: 2915390090
• European Community (EC) Number: 252-397-7,682-359-9
• UNII: 09M3TB6O62
• DSSTox Substance ID: DTXSID0035291
• Nikkaji Number: J1.015.683A,J289.916G
• Wikidata: Q27236489
• Metabolomics Workbench ID: 3874
• Mol file: 35148-19-7.mol

Synonyms:(E)-9-dodecenyl acetate;9-dodecenyl acetate;9-dodecenyl acetate, (cis)-isomer;9-dodecenyl acetate, (trans)-isomer

Chemical Property of (E)-9-Dodecenyl acetate

Chemical Property:

• Vapor Pressure: 0.00114mmHg at 25°C
• Refractive Index: 1.4445 (22℃)
• Boiling Point: 300.1°Cat760mmHg
• Flash Point: 96.5°C
• PSA: 26.30000
• Density: 0.881g/cm³
• LogP: 4.24640
• 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:

95% ^*data from raw suppliers

(9E)-Dodecen-1-ylAcetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Low toxicity by ingestion and skin contact.
• Hazard Codes: Low toxicity by ingestion and skin contact.

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC=CCCCCCCCCOC(=O)C
• Isomeric SMILES: CC/C=C/CCCCCCCCOC(=O)C
• Uses: (9E)-Dodecen-1-yl Acetate can be used in biological study of identification of the female sex pheromone of the Leafroller Proeulia triquetra Obraztsov (Lepidoptera: Tortricidae).

Technology Process of (E)-9-Dodecenyl acetate

There total 59 articles about (E)-9-Dodecenyl 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%

(E)-9-dodecen-1-ol (35237-62-8) + acetic anhydride (108-24-7) → (E)-9-dodecenyl acetate (35148-19-7)

Guidance literature:

With pyridine; dmap; at 25 ℃; for 0.5h;

DOI:10.1007/BF00961235

Reference yield: 98.0%

Δ9-Dodecenyl acetate (16974-34-8) → (E)-9-dodecenyl acetate (35148-19-7)

Guidance literature:

With urea; In methanol; for 16h; Ambient temperature;

Reference yield: 97.0%

(E)-9-dodecen-1-ol (35237-62-8) + acetyl chloride (75-36-5) → (E)-9-dodecenyl acetate (35148-19-7)

Guidance literature:

With triethylamine; In diethyl ether; at 0 ℃;

DOI:10.1134/S107042801706001X

upstream raw materials:

Δ⁹-Dodecenyl acetate

(6-bromohexyl)-trimethylsilyl ether

(E)-hex-3-en-1-yl 4-methylbenzenesulfonate

potassium acetate