Decanoic acid, 2-methyl-, ethyl ester

Base Information

Chemical Name:Decanoic acid, 2-methyl-, ethyl ester
CAS No.:126784-41-6
Molecular Formula:C13H26O2
Molecular Weight:214.348
Hs Code.:
DSSTox Substance ID:DTXSID70474113
Nikkaji Number:J1.335.962H
Mol file:126784-41-6.mol

Synonyms:ethyl 2-methyldecanoate;ethyl-2-methyldecanoate

Suppliers and Price of Decanoic acid, 2-methyl-, ethyl 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

Total 3 raw suppliers

Chemical Property of Decanoic acid, 2-methyl-, ethyl ester

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:10
Exact Mass:214.193280068
Heavy Atom Count:15
Complexity:155

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Decanoic acid, 2-methyl-, ethyl ester

There total 1 articles about Decanoic acid, 2-methyl-, ethyl 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:

: 64-17-5
ethanol

: 872-05-9,17438-89-0,25189-70-2
1-Decene

: 201230-82-2
carbon monoxide

: 627-90-7
ethyl undecanoate

: 126784-41-6
ethyl (R,S)-2-methyldecanoate

Guidance literature:: With titanium(IV) isopropylate; lithium chloride; palladium dichloride; 1,3,5,7-tetramethyl-8-phenyl-2,4,6-trioxa-8-phosphatricyclo[3.3.1.13,7]decane; In 1,2-dimethoxyethane; at 110 ℃; for 22h; under 18100.7 Torr; Overall yield = 67 %; regioselective reaction; Autoclave;
DOI:10.1021/acs.joc.5b00851