(E)-11-Tetradecen-1-ol

Base Information

• Chemical Name: (E)-11-Tetradecen-1-ol
• CAS No.: 35153-18-5
• Molecular Formula: C14H28 O
• Molecular Weight: 212.376
• Hs Code.: 2905290000
• European Community (EC) Number: 252-402-2
• UNII: P2B0SE7A0P
• DSSTox Substance ID: DTXSID0035293
• Nikkaji Number: J1.015.721H,J683A
• Metabolomics Workbench ID: 3263
• Mol file: 35153-18-5.mol

Synonyms:(E)-11-Tetradecen-1-ol;35153-18-5;11-Tetradecen-1-ol, (E)-;11E-Tetradecen-1-ol;(E)-tetradec-11-en-1-ol;e-11-tetradecen-1-ol;11-Tetradecen-1-ol, (11E)-;(E)-Tetradec-11-enol;(11E)-Tetradecen-1-ol;11-Tetradecen-1-ol;EINECS 252-402-2;UNII-P2B0SE7A0P;EPA Pesticide Chemical Code 129020;P2B0SE7A0P;AI3-35944;C14H28O;E-11-Tetradecenol;(11E)-tetradecenol;11-Tetradecenol, E;11-tetradecene-1-ol;(E)-11-tetradecenol;trans-tetradec-11-enol;(11E)-tetradec-11-enol;SCHEMBL808503;(11E)-11-Tetradecen-1-ol;DTXSID0035293;(11E)-tetradec-11-en-1-ol;CHEBI:186758;LMFA05000173;STL562230;AKOS030490245;TETRADECEN-1-OL, (E)-11-;LS-148928;Q27286034

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

Chemical Property:

• Vapor Pressure: 0.000445mmHg at 25°C
• Refractive Index: 1.4562 (589.3 nm 20℃)
• Boiling Point: 280.7°Cat760mmHg
• Flash Point: 121.3°C
• PSA: 20.23000
• Density: 0.846g/cm³
• LogP: 4.45580
• XLogP3: 5.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 11
• Exact Mass: 212.214015512
• Heavy Atom Count: 15
• Complexity: 129

Purity/Quality:

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

(11E)-Tetradecen-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC=CCCCCCCCCCCO
• Isomeric SMILES: CC/C=C/CCCCCCCCCCO
• Uses: (11E)-Tetradecen-1-ol is a sex pheromone gland of the lightbrown apple moth. A component of a congener Ostrinia latipennis moth species.

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

There total 55 articles about (E)-11-Tetradecen-1-ol 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%

13-tetradec-11-yn-1-ol (33925-73-4) → (E)-11-tetradecen-1-ol (35153-18-5)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; diethylene glycol dimethyl ether; at 140 ℃; for 10h;

DOI:10.1007/BF00580036

Reference yield: 95.0%

14-tetrahydropyranyloxy-2(E)-tetradecene (57586-92-2) → (E)-11-tetradecen-1-ol (35153-18-5)

Guidance literature:

With hydrogenchloride; In methanol; for 4h;

Reference yield: 90.9%

methyl (E)-11-tetradecenoate (119136-11-7) → (E)-11-tetradecen-1-ol (35153-18-5)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; for 15h;

upstream raw materials:

(E)-1-bromo-3-hexene

8-bromooctanol

13-tetradec-11-yn-1-ol

(E)-tetradec-11-en-1-yl acetate

Downstream raw materials:

E,Z-11-tetradecen-1-al

(E)-tetradec-11-en-1-yl acetate