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Encyclopedia

Tefuryltrione

Base Information Edit
  • Chemical Name:Tefuryltrione
  • CAS No.:473278-76-1
  • Molecular Formula:C20H23ClO7S
  • Molecular Weight:442.917
  • Hs Code.:
  • European Community (EC) Number:695-022-6
  • UNII:31009O776L
  • DSSTox Substance ID:DTXSID9058105
  • Nikkaji Number:J2.715.929J
  • Wikidata:Q27255985
  • Mol file:473278-76-1.mol
Tefuryltrione

Synonyms:tefuryltrione

Suppliers and Price of Tefuryltrione
Supply Marketing:Edit
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 Tefuryltrione Edit
Chemical Property:
  • Vapor Pressure:1.18E-18mmHg at 25°C 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:7
  • Exact Mass:442.0853019
  • Heavy Atom Count:29
  • Complexity:728
Purity/Quality:

99.9% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CS(=O)(=O)C1=C(C(=C(C=C1)C(=O)C2C(=O)CCCC2=O)Cl)COCC3CCCO3
Technology Process of Tefuryltrione

There total 4 articles about Tefuryltrione 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:
methyl 2-chloro-4-(methylsulfonyl)-3-(((tetrahydrofuran-2-yl)methoxy)methyl)benzoate; 1,3-cylohexanedione; With ethylenediamine; In acetonitrile; at 20 ℃; for 1.5h;
With acetonitrile; at 20 ℃; for 2h; Time;
Guidance literature:
Multi-step reaction with 4 steps
1.1: thionyl chloride / 3 h / 60 °C
2.1: 2,2'-azobis(isobutyronitrile) / dichloromethane / 3 h / 60 °C
2.2: 7.5 h / 70 °C
3.1: sodium carbonate; zinc(II) sulfate / tetrahydrofuran / 2.5 h / Cooling with ice
4.1: ethylenediamine / acetonitrile / 3 h / 20 °C
With thionyl chloride; 2,2'-azobis(isobutyronitrile); sodium carbonate; ethylenediamine; zinc(II) sulfate; In tetrahydrofuran; dichloromethane; acetonitrile;
Guidance literature:
Multi-step reaction with 3 steps
1.1: 2,2'-azobis(isobutyronitrile) / dichloromethane / 3 h / 60 °C
1.2: 7.5 h / 70 °C
2.1: sodium carbonate; zinc(II) sulfate / tetrahydrofuran / 2.5 h / Cooling with ice
3.1: ethylenediamine / acetonitrile / 3 h / 20 °C
With 2,2'-azobis(isobutyronitrile); sodium carbonate; ethylenediamine; zinc(II) sulfate; In tetrahydrofuran; dichloromethane; acetonitrile;
Refernces Edit
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