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Undecanoic acid, 2-acetyl-, methyl ester

Base Information
  • Chemical Name:Undecanoic acid, 2-acetyl-, methyl ester
  • CAS No.:113081-88-2
  • Molecular Formula:C14H26O3
  • Molecular Weight:242.359
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30442813
  • Nikkaji Number:J132.519A
  • Mol file:113081-88-2.mol
Undecanoic acid, 2-acetyl-, methyl ester

Synonyms:Undecanoic acid, 2-acetyl-, methyl ester;113081-88-2;DTXSID30442813;2-Acetylundecylic acid methyl ester

Suppliers and Price of Undecanoic acid, 2-acetyl-, methyl 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 2 raw suppliers
Chemical Property of Undecanoic acid, 2-acetyl-, methyl ester
Chemical Property:
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:11
  • Exact Mass:242.18819469
  • Heavy Atom Count:17
  • Complexity:224
Purity/Quality:

99.90% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCC(C(=O)C)C(=O)OC
Technology Process of Undecanoic acid, 2-acetyl-, methyl ester

There total 6 articles about Undecanoic acid, 2-acetyl-, methyl 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:
Guidance literature:
With tetra-(n-butyl)ammonium iodide; sodium hydride; In 1,2-dimethoxyethane; at 80 ℃; for 20h;
DOI:10.1021/jo952098j
Guidance literature:
acetoacetic acid methyl ester; With sodium; In methanol; at 0 ℃;
nonylhalide; In methanol; Reflux;
DOI:10.1002/pca.2466
Guidance literature:
Multi-step reaction with 4 steps
1.1: hydrogen bromide; sulfuric acid / 1 h / 0 - 120 °C
2.1: sodium ethanolate / ethanol / 0.5 h
2.2: 6 h / 80 °C
3.1: sodium hydroxide / water / 4 h / 100 °C
3.2: 20 °C
4.1: sulfuric acid / 1 h / 90 °C
With sulfuric acid; hydrogen bromide; sodium ethanolate; sodium hydroxide; In ethanol; water;
DOI:10.1255/ejms.1402
upstream raw materials:

1-Bromononane

acetoacetic acid methyl ester

methanol

nonyl alcohol

Downstream raw materials:

C15H28O3

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