Methyl beta-eleostearate

Base Information

• Chemical Name: Methyl beta-eleostearate
• CAS No.: 16195-77-0
• Molecular Formula: C₁₉H₃₂O₂
• Molecular Weight: 292.462
• UNII: U6YHQ05JZS
• Nikkaji Number: J2.300.465H
• Wikidata: Q27290772
• Mol file: 16195-77-0.mol

Synonyms:Bollex;Methyl beta-eleostearate;U6YHQ05JZS;EPA Pesticide Chemical Code 118501;Methyl ester of (Z,E,E)-9,11,13-octadecatrienoic acid;9,11,13-Octadecatrienoic acid, methyl ester, (9E,11E,13E)-;9,11,13-OCTADECATRIENOIC ACID, METHYL ESTER, (Z,E,E)-;16195-77-0;4238-03-3;UNII-U6YHQ05JZS;SCHEMBL11316636;SCHEMBL11316639;beta-Eleostearic acid methyl ester;METHYL .BETA.-ELEOSTEARATE;LS-97725;.BETA.-ELEOSTEARIC ACID METHYL ESTER;Q27290772;(9E,11E,13E)-9,11,13-Octadecatrienoic acid methyl ester;trans,trans,trans-octadeca-9,11,13-trienoic acid methyl ester

Chemical Property of Methyl beta-eleostearate

Chemical Property:

• Vapor Pressure: 3.52E-06mmHg at 25°C
• Boiling Point: 386.5°C at 760 mmHg
• Flash Point: 108.2°C
• Density: 0.895g/cm³
• XLogP3: 6.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 14
• Exact Mass: 292.240230259
• Heavy Atom Count: 21
• Complexity: 314

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC=CC=CC=CCCCCCCCC(=O)OC
• Isomeric SMILES: CCCC/C=C/C=C/C=C/CCCCCCCC(=O)OC

Technology Process of Methyl beta-eleostearate

There total 1 articles about Methyl beta-eleostearate 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:

methyl ester of azelaic acid aldehyde (1931-63-1) + ((2E,4Z)-Nona-2,4-dienyl)-triphenyl-phosphonium; chloride → α-Elaeostearinsaeuremethylester (16195-77-0)

Guidance literature:

Multistep reaction; (i) nBuLi, hexane, (ii) /BRN= 1766823/;

DOI:10.1007/BF00915661

upstream raw materials:

methyl ester of azelaic acid aldehyde