(E)-11-Tetradecen-1-ol acetate

Base Information

• Chemical Name: (E)-11-Tetradecen-1-ol acetate
• CAS No.: 33189-72-9
• Molecular Formula: C16H30O2
• Molecular Weight: 254.413
• European Community (EC) Number: 251-401-4
• UNII: UXJ691Z784
• DSSTox Substance ID: DTXSID1035286
• Nikkaji Number: J676I,J891.997F
• Wikidata: Q27291316
• Metabolomics Workbench ID: 3930
• ChEMBL ID: CHEMBL3182789
• Mol file: 33189-72-9.mol

Synonyms:(E)-11-tetradecen-1-acetate;11-tetradecenyl acetate;11-tetradecenyl acetate, (E)-isomer;11-tetradecenyl acetate, (Z)-isomer

Chemical Property of (E)-11-Tetradecen-1-ol acetate

Chemical Property:

• Vapor Pressure: 0.000416mmHg at 25°C
• Melting Point: <25℃
• Refractive Index: 1.4481 (589.3 nm 20℃)
• Boiling Point: 316.2 °C at 760 mmHg
• Flash Point: 87.2 °C
• PSA: 26.30000
• Density: 0.878 g/cm³
• LogP: 5.02660
• Storage Temp.: −20°C
• Solubility.: Chloroform (Slightly), DMSO (Slightly)
• XLogP3: 5.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 13
• Exact Mass: 254.224580195
• Heavy Atom Count: 18
• Complexity: 209

Purity/Quality:

98%,99%, ^*data from raw suppliers

trans-11-Tetradecenylacetate 92% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC=CCCCCCCCCCCOC(=O)C
• Isomeric SMILES: CC/C=C/CCCCCCCCCCOC(=O)C
• Uses: (11E)-Tetradecen-1-yl Acetate is found in the sex pheromones of moths.

Technology Process of (E)-11-Tetradecen-1-ol acetate

There total 68 articles about (E)-11-Tetradecen-1-ol 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: 95.0%

(E)-11-tetradecen-1-ol (35153-18-5) + acetic anhydride (108-24-7) → (E)-tetradec-11-en-1-yl acetate (33189-72-9,39298-52-7)

Guidance literature:

With pyridine; In diethyl ether;

Reference yield: 92.0%

14-tetrahydropyranyloxy-2(E)-tetradecene (57586-92-2) + acetyl chloride (75-36-5) → (E)-tetradec-11-en-1-yl acetate (33189-72-9,39298-52-7)

Guidance literature:

In pyridine; acetic acid; at 0 ℃; for 13h;

Reference yield: 88.0%

potassium acetate (127-08-2) + 1-chloro-11E-tetradecene (83748-51-0) → (E)-tetradec-11-en-1-yl acetate (33189-72-9,39298-52-7)

Guidance literature:

With potassium iodide; In acetic acid; for 20h; Heating;

upstream raw materials:

(Z)-11-tetradecenyl acetate

1-bromobut-1-yne

9-decen-1-yl acetate

potassium acetate

Downstream raw materials:

(Z)-11-tetradecenyl acetate

(E)-11-tetradecen-1-ol

E,Z-11-tetradecen-1-al