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Undecyl acrylate

Base Information
  • Chemical Name:Undecyl acrylate
  • CAS No.:20690-61-3
  • Molecular Formula:C14H26O2
  • Molecular Weight:226.359
  • Hs Code.:2916129000
  • European Community (EC) Number:243-973-9
  • DSSTox Substance ID:DTXSID60174751
  • Nikkaji Number:J107.539J
  • Wikidata:Q83044869
  • Mol file:20690-61-3.mol
Undecyl acrylate

Synonyms:Undecyl acrylate;20690-61-3;undecyl prop-2-enoate;EINECS 243-973-9;AI3-33811;Undecylacrylate;Acrylic acid undecyl ester;SCHEMBL76002;2-Propenoic acid, undecyl ester;DTXSID60174751;MFCD00048415;FT-0638032

Suppliers and Price of Undecyl acrylate
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
  • UNDECYL ACRYLATE 98.00%
  • 1G
  • $ 1166.55
Total 6 raw suppliers
Chemical Property of Undecyl acrylate
Chemical Property:
  • Vapor Pressure:0.00228mmHg at 25°C 
  • Boiling Point:288.8°C at 760 mmHg 
  • Flash Point:102.5°C 
  • PSA:26.30000 
  • Density:0.876g/cm3 
  • LogP:4.24640 
  • XLogP3:5.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:12
  • Exact Mass:226.193280068
  • Heavy Atom Count:16
  • Complexity:176
Purity/Quality:

98%Min *data from raw suppliers

UNDECYL ACRYLATE 98.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCOC(=O)C=C
Technology Process of Undecyl acrylate

There total 6 articles about Undecyl acrylate 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 triphenylphosphine; In toluene; for 24h; Heating;
DOI:10.1016/S0040-4039(03)01272-3
Guidance literature:
With 2,2'-azobis(isobutyronitrile); tertbutyltin hydride; In benzene; for 3h; Heating;
DOI:10.1021/ja00250a036
Guidance literature:
Multi-step reaction with 4 steps
1: carbon tetrabromide, triphenylphosphine / tetrahydrofuran / 20 h / Ambient temperature
2: triethylamine / CH2Cl2 / Ambient temperature
3: sodium iodide / butan-2-one / 3 h / Heating
4: 12 percent / tertbutyltin hydride, AIBN / benzene / 3 h / Heating
With 2,2'-azobis(isobutyronitrile); carbon tetrabromide; tertbutyltin hydride; triethylamine; triphenylphosphine; sodium iodide; In tetrahydrofuran; dichloromethane; butanone; benzene;
DOI:10.1021/ja00250a036
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