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Dotriacontane-16,17-dione

Base Information
  • Chemical Name:Dotriacontane-16,17-dione
  • CAS No.:32153-87-0
  • Molecular Formula:C32H62O2
  • Molecular Weight:478.843
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20572572
  • Nikkaji Number:J1.160.187A
  • Wikidata:Q82460959
  • Mol file:32153-87-0.mol
Dotriacontane-16,17-dione

Synonyms:DOTRIACONTANE-16,17-DIONE;32153-87-0;SCHEMBL1441291;DTXSID20572572

Suppliers and Price of Dotriacontane-16,17-dione
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Dotriacontane-16,17-dione
Chemical Property:
  • XLogP3:14.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:29
  • Exact Mass:478.47498122
  • Heavy Atom Count:34
  • Complexity:389
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCCCC(=O)C(=O)CCCCCCCCCCCCCCC
Technology Process of Dotriacontane-16,17-dione

There total 7 articles about Dotriacontane-16,17-dione 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 oxygen; vanadium(V) oxychloride; In acetonitrile; for 13.5h; Heating;
DOI:10.1039/a903622i
Guidance literature:
With ruthenium trichloride; bromamine T; In water; acetonitrile; at 80 ℃; for 1h; pH=8.4;
DOI:10.1081/SCC-200048974
Guidance literature:
Multi-step reaction with 3 steps
1: tetrakis(acetonitrile)copper(I)tetrafluoroborate; [2,2]bipyridinyl; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; 1-methyl-1H-imidazole; oxygen / acetonitrile / 1.5 h / 60 °C / Schlenk technique
2: 3-benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazol-3-ium chloride; triethylamine / ethanol / 3 h / 80 °C / Inert atmosphere
3: oxygen; vanadium(V) oxytrichloride / acetonitrile / 24 h / 65 °C
With 1-methyl-1H-imidazole; [2,2]bipyridinyl; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrakis(acetonitrile)copper(I)tetrafluoroborate; vanadium(V) oxytrichloride; oxygen; 3-benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazol-3-ium chloride; triethylamine; In ethanol; acetonitrile;
DOI:10.1002/chem.201502333
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