(Z)-5-Decenyl acetate

Base Information

• Chemical Name: (Z)-5-Decenyl acetate
• CAS No.: 67446-07-5
• Deprecated CAS: 90678-35-6
• Molecular Formula: C12H22 O2
• Molecular Weight: 198.305
• European Community (EC) Number: 266-693-9
• DSSTox Substance ID: DTXSID401015024
• Nikkaji Number: J247.951F
• Metabolomics Workbench ID: 3853
• Mol file: 67446-07-5.mol

Synonyms:(Z)-5-Decenyl acetate;67446-07-5;5Z-Decenyl acetate;[(Z)-dec-5-enyl] acetate;Z-5-Decen-1-ylacetate;(5Z)-Decenyl Acetate;Z-5-Decen-1-yl acetate;cis-5-Decen-1-yl acetate;5-Decen-1-ol, 1-acetate, (5Z)-;EINECS 266-693-9;z-5-decenyl acetate;5-Decen-1-ol,1-acetate, (5Z)-;5-Decen-1-ol, acetate, (5Z)-;(Z)-5-Decenyl=acetate;(5Z)-5-Decenyl acetate;(Z)-5-Decen-1-yl acetate;Acetic acid dec-5-enyl ester;SCHEMBL1301852;CHEBI:179184;VTUFOIHYMMMNOM-SREVYHEPSA-N;5-Decen-1-ol, acetate, (Z)-;DTXSID401015024;LMFA07010208;AKOS006283056;5Z-Decenyl acetate CAS 67446-07-5;E75976

Chemical Property of (Z)-5-Decenyl acetate

Chemical Property:

• Vapor Pressure: 0.192mmHg at 25°C
• Refractive Index: 1.4425 (20℃)
• Boiling Point: 210.5oC at 760 mmHg
• Flash Point: 62.2oC
• PSA: 26.30000
• Density: 0.886g/cm3
• LogP: 3.46620
• Storage Temp.: 2-8°C
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 9
• Exact Mass: 198.161979940
• Heavy Atom Count: 14
• Complexity: 162

Purity/Quality:

93% ^*data from raw suppliers

(5Z)-DecenylAcetate ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC=CCCCCOC(=O)C
• Isomeric SMILES: CCCC/C=C\CCCCOC(=O)C
• Uses: (5Z)-Decenyl Acetate is an insect sex pheromone semiochemical compound. Most abundant constituents in the oil of Heracleum crenatifolium.

Technology Process of (Z)-5-Decenyl acetate

There total 46 articles about (Z)-5-Decenyl 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%

(Z)-dec-5-en-1-ol (51652-47-2) + acetic anhydride (108-24-7) → (Z)-5-decenyl acetate (67446-07-5)

Guidance literature:

In pyridine;

DOI:10.1081/SCC-120018943

Reference yield: 93.0%

(Z)-dec-5-en-1-ol (51652-47-2) + acetyl chloride (75-36-5) → (Z)-5-decenyl acetate (67446-07-5)

Guidance literature:

With pyridine; In hexane; at 12 - 20 ℃; for 2h;

DOI:10.1007/BF02495779

Reference yield: 81.0%

dec-5-yn-1-yl acetate (64275-65-6) → (Z)-5-decenyl acetate (67446-07-5)

Guidance literature:

With hydrogen; nickel; ethylenediamine; In ethanol; at 20 ℃;

DOI:10.1007/s11167-005-0217-z

upstream raw materials:

(Z)-dec-5-en-1-ol

acetic anhydride

(E)-5-decen-1-ol

acetyl chloride

Downstream raw materials:

(Z)-dec-5-en-1-ol

Refernces

• 1、 Gregori, Bernhard J.,Nowakowski, Michal,Schoch, Anke,P?llath, Simon,Zweck, Josef,Bauer, Matthias,Jacobi von Wangelin, Axel. "Stereoselective Chromium-Catalyzed Semi-Hydrogenation of Alkynes". . p. 5359 - 5363. Retrieved 2020/09/03.
• 2、 Jindal, Rani,Devi, Aarti,Kad, Goverdhan L.,Singh, Jasvinder. "Synthesis of heneicos-6(Z)-en-11-one, dec-5(Z)-en-l-yl acetate, dec-5(Z)-En-1-y1-3-methylbutanoate (insect sex pheromones)". experimental part. p. 495 - 499. Retrieved 2010/10/20.