9-Octadecenoyl chloride

Base Information

• Chemical Name: 9-Octadecenoyl chloride
• CAS No.: 7378-94-1
• Molecular Formula: C18H33ClO
• Molecular Weight: 300.912
• Mol file: 7378-94-1.mol

Synonyms:9-Octadecenoyl chloride;oleoyl chloride;octadec-9-enoylchloride;(E)-Octadec-9-enoyl chloride;

Chemical Property of 9-Octadecenoyl chloride

Chemical Property:

• PSA: 17.07000
• LogP: 6.78930

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 9-Octadecenoyl chloride

There total 3 articles about 9-Octadecenoyl chloride 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: 85.0%

→ 9,12-octadecadienoyl chloride (7372-07-8) + octadec-9-enoyl chloride (7378-94-1)

Guidance literature:

Reference yield:

Elaidic acid (112-79-8,2027-47-6) → elaidoyl chloride (112-77-6,7378-94-1,7459-35-0)

Guidance literature:

With thionyl chloride; at 50 ℃;

Reference yield:

oxalyl dichloride (79-37-8) + Elaidic acid (112-79-8,2027-47-6) → elaidoyl chloride (112-77-6,7378-94-1,7459-35-0)

Guidance literature:

at 65 - 80 ℃;

DOI:10.1021/ja01230a040 DOI:10.1021/ja01230a041

upstream raw materials:

oxalyl dichloride

Elaidic acid

Downstream raw materials:

1-Palmito-2,3-dielaidin

1-Stearo-2,3-dielaidin

2-(oleamido)propane-1,3-diol

Refernces

• 1、 -. "OLEIC ACID DERIVATIVES, PHARMACEUTICAL COMPOSITION OR FOOD COMPOSITION COMPRISING SAID OLEIC ACID DERIVATIVES, AND THEIR USES". Page/Page column 29. . Retrieved 2019/12/25.
• 2、 Takao, Koichi,Noguchi, Kaori,Hashimoto, Yosuke,Shirahata, Akira,Sugita, Yoshiaki. "Synthesis and evaluation of fatty acid amides on the N-oleoylethanolamide-like activation of peroxisome proliferator activated receptor α". . p. 278 - 285. Retrieved 2015/04/22.