(8Z)-8-Hexadecene

Base Information

• Chemical Name: (8Z)-8-Hexadecene
• CAS No.: 35507-10-9
• Molecular Formula: C16H32
• Molecular Weight: 0.00000
• UNII: 72L4ZW9CO2
• Nikkaji Number: J678.191H
• Wikidata: Q27266083
• Mol file: 35507-10-9.mol

Synonyms:(Z)-hexadec-8-ene;Z-8-Hexadecene;(Z)-8-Hexadecene;(8Z)-8-Hexadecene;cis-8-Hexadecene;8-Hexadecene, (8Z)-;35507-10-9;8-Hexadecene, (Z)-;72L4ZW9CO2;UNII-72L4ZW9CO2;(8Z)-8-Hexadecene #;KWEAIXVWPDMXCR-NXVVXOECSA-N;Q27266083

Chemical Property of (8Z)-8-Hexadecene

Chemical Property:

• PSA: 0.00000
• LogP: 0.00000
• XLogP3: 7.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 12
• Exact Mass: 224.250401021
• Heavy Atom Count: 16
• Complexity: 119

Purity/Quality:

99% ^*data from raw suppliers

(Z)-8-Hexadecene ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCCCCCC=CCCCCCCC
• Isomeric SMILES: CCCCCCC/C=C\CCCCCCC
• Uses: (Z)-8-Hexadecene is aliphatic alkane that is a component of the essential oil in Corydalis straminea Maxim. (Z)-8-Hexadecene is used in the preparation of fatty alcohols with potential for application in commercial products, such as bio-diesel, lubricants, greases, and cosmetics.

Technology Process of (8Z)-8-Hexadecene

There total 23 articles about (8Z)-8-Hexadecene 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: 53.0%

(8Z)-hexadecene-5,12-dimesylate → (Z)-Hexadec-8-ene (35507-10-9)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; Inert atmosphere; Reflux;

DOI:10.1016/j.phytochem.2017.05.011

Reference yield:

hexadec-8-yne (19781-86-3) → (Z)-Hexadec-8-ene (35507-10-9)

Guidance literature:

With hydrogen; In 1,4-dioxane; methanol; at 30 ℃; for 0.166667h; under 760.051 Torr; Schlenk technique;

DOI:10.1021/acscatal.8b04653

Reference yield:

C16H34O4S → (Z)-Hexadec-8-ene (35507-10-9) + (E)-1,2-diheptylethene (74533-91-8)

Guidance literature:

With 5-Chloro-1-phenyltetrazole; potassium tert-butylate; In tetrahydrofuran; at -78 - 20 ℃; for 18h; Overall yield = 0.118 g; stereoselective reaction; Inert atmosphere; Schlenk technique;

DOI:10.1039/c9ob01563a

upstream raw materials:

Octanal

n-octyltriphenylphosphoniumbromide

((CH₃)3C₆H₂)2BCHLiC₇H₁₅

dioctylsulfone