Methanesulfonic acid erucyl ester

Base Information

Chemical Name:Methanesulfonic acid erucyl ester
CAS No.:102542-59-6
Molecular Formula:C₂₃H₄₆O₃S
Molecular Weight:402.682
Hs Code.:
European Community (EC) Number:634-401-2
DSSTox Substance ID:DTXSID80407972
Mol file:102542-59-6.mol

Synonyms:Methanesulfonic acid erucyl ester;102542-59-6;docos-13-enyl methanesulfonate;13-Docosen-1-ol,1-methanesulfonate;Erucyl Methane Sulfate;DTXSID80407972

Suppliers and Price of Methanesulfonic acid erucyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
CIS-13-DOCOSENYL METHANESULFONATE 95.00%
5MG
$ 505.49

Total 6 raw suppliers

Chemical Property of Methanesulfonic acid erucyl ester

Chemical Property:

PSA：51.75000
LogP:8.64130
Storage Temp.:−20°C
XLogP3:9.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:21
Exact Mass:402.31676650
Heavy Atom Count:27
Complexity:410

Purity/Quality:

98%min ^*data from raw suppliers

CIS-13-DOCOSENYL METHANESULFONATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCC=CCCCCCCCCCCCCOS(=O)(=O)C

Technology Process of Methanesulfonic acid erucyl ester

There total 3 articles about Methanesulfonic acid erucyl ester 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: 86.0%

: 629-98-1
erucyl alcohol

: 124-63-0
methanesulfonyl chloride

: 102542-59-6,50995-22-7
erucyl mesylate

Guidance literature:: With triethylamine; In 2-methyltetrahydrofuran; at 0 - 20 ℃; for 1.5h; Solvent; Inert atmosphere;

Reference yield:

: 1120-34-9
methyl cis-13-docosenoate

: 102542-59-6,50995-22-7
erucyl mesylate

Guidance literature:: Multi-step reaction with 2 steps

1: lithium alanate; diethyl ether

2: pyridine

With pyridine; lithium aluminium tetrahydride; diethyl ether;
DOI:10.1139/v57-107