Z-9-Hexadecen-1-ol acetate

Base Information

• Chemical Name: Z-9-Hexadecen-1-ol acetate
• CAS No.: 34010-20-3
• Molecular Formula: C18H34 O2
• Molecular Weight: 282.467
• Hs Code.: 2915390090
• UNII: Z3V5G565CA
• Nikkaji Number: J678E
• Metabolomics Workbench ID: 4013
• Mol file: 34010-20-3.mol

Synonyms:34010-20-3;Z-9-Hexadecen-1-ol acetate;CIS-9-HEXADECENYL ACETATE;9Z-Hexadecenyl acetate;[(Z)-hexadec-9-enyl] acetate;9-Hexadecen-1-ol, acetate, (Z)-;(z)-9-hexadecenyl acetate;AI3-33810;cis-9-Hexadecen-1-ol acetate;Z-9-hexadecenyl acetate;9-Hexadecenyl acetate, cis-;(9Z)-9-Hexadecenyl acetate;SCHEMBL593384;(Z)-1-Acetoxy-9-hexadecene;cis-9-hexadecen-1-yl acetate;Z3V5G565CA;1-Acetoxy-(Z)-hexadec-9-ene;(9Z)-9-Hexadecenyl acetate #;(Z)-9-Hexadecen-1-ol acetate;VAKBQCYSUVICLV-HJWRWDBZSA-N;Z-9-16-Ac;LMFA07010368;9-Hexadecen-1-ol, acetate, (9Z)-;9Z-HEXADECENYL ACETATE , 95 %;(9Z)-HEXADEC-9-EN-1-YL ACETATE;9Z-Hexadecenyl acetate CAS 34010-20-3

Chemical Property of Z-9-Hexadecen-1-ol acetate

Chemical Property:

• Vapor Pressure: 1.61E-05mmHg at 25°C
• Boiling Point: 365°C at 760 mmHg
• Flash Point: 98.7°C
• PSA: 26.30000
• Density: 0.875g/cm³
• LogP: 5.80680
• Storage Temp.: -20°C
• XLogP3: 6.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 15
• Exact Mass: 282.255880323
• Heavy Atom Count: 20
• Complexity: 234

Purity/Quality:

99.3% ^*data from raw suppliers

CIS-9-HEXADECENYL ACETATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCC=CCCCCCCCCOC(=O)C
• Isomeric SMILES: CCCCCC/C=C\CCCCCCCCOC(=O)C

Technology Process of Z-9-Hexadecen-1-ol acetate

There total 1 articles about Z-9-Hexadecen-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:

9-bromononan-1-ol (55362-80-6) → hexadec-cis-9-en-1-ol acetate (34010-20-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 90 percent / acetonitrile

2: 71 percent / DMSO, NaY / tetrahydrofuran / 0.5 h

3: pyridine

With pyridine; dimethyl sulfoxide; In tetrahydrofuran; acetonitrile;

DOI:10.1271/bbb1961.44.257

Reference yield: 82.0%

hexadec-cis-9-en-1-ol acetate (34010-20-3) → palmitoleyl alcohol (10378-01-5)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; for 5h;

DOI:10.1007/BF00630187

Reference yield:

hexadec-cis-9-en-1-ol acetate (34010-20-3) → (Z)-9-hexadecenal (56219-04-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 82 percent / LiAlH₄ / diethyl ether / 5 h / 20 °C

2: 67 percent / pyridinium chlorochromate / CH₂Cl₂ / 0.67 h / 20 °C

With lithium aluminium tetrahydride; pyridinium chlorochromate; In diethyl ether; dichloromethane;

DOI:10.1007/BF00630187

upstream raw materials:

9-bromononan-1-ol

Downstream raw materials:

palmitoleyl alcohol

9-acetoxynonal

(Z)-9-hexadecenal

Refernces