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Undecaprenol

Base Information
  • Chemical Name:Undecaprenol
  • CAS No.:15575-14-1
  • Molecular Formula:C55H90O
  • Molecular Weight:767.319
  • Hs Code.:
  • European Community (EC) Number:630-882-8
  • Metabolomics Workbench ID:29114
  • Nikkaji Number:J28.588I,J3.481.021D
  • Wikidata:Q27101987
  • Mol file:15575-14-1.mol
Undecaprenol

Synonyms:ficaprenol;undecaprenol;undecaprenol, (Z,Z,Z,Z,Z,Z,Z,E,E,E)-isomer

Suppliers and Price of Undecaprenol
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 4 raw suppliers
Chemical Property of Undecaprenol
Chemical Property:
  • Vapor Pressure:6.93E-28mmHg at 25°C 
  • Boiling Point:777°Cat760mmHg 
  • PKA:14.69±0.10(Predicted) 
  • Flash Point:114.9°C 
  • PSA:20.23000 
  • Density:0.89g/cm3 
  • LogP:18.20990 
  • Storage Temp.:−20°C 
  • XLogP3:19.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:31
  • Exact Mass:766.69916749
  • Heavy Atom Count:56
  • Complexity:1410
Purity/Quality:

96% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
  • Statements: 45-46-20/21/22-36/37/38 
  • Safety Statements: 53-23-26-36/37/39-45 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C
  • Isomeric SMILES:CC(=CCC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CC/C(=C/CO)/C)/C)/C)/C)/C)/C)/C)/C)/C)/C)C
Technology Process of Undecaprenol

There total 3 articles about Undecaprenol 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 potassium carbonate; In tetrahydrofuran; methanol; at 20 ℃; for 18h; Inert atmosphere;
DOI:10.1039/d0cc03388j
Guidance literature:
1-((2Z,6Z,10Z,14Z,18Z,22Z,26Z,30E,34E,38E)-1-benzyloxy-17-tosyl-3,7,11,15,19,23,27,31,35,39,43-undecamethyltetratetraconta-2,6,10,14,18,22,26,30,34,38,42-undecaen-9-yl)sulfonyl-4-methylbenzene; With lithium; ethylamine; In diethyl ether; at -78 ℃; for 1h; Inert atmosphere;
With isoprene; In methanol; diethyl ether; Inert atmosphere;
DOI:10.1016/j.tet.2009.06.032
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