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Futoquinol

Base Information
  • Chemical Name:Futoquinol
  • CAS No.:28178-92-9
  • Molecular Formula:C21H22O5
  • Molecular Weight:354.403
  • Hs Code.:
  • ChEMBL ID:CHEMBL498296
  • DSSTox Substance ID:DTXSID001110595
  • Metabolomics Workbench ID:70447
  • Wikidata:Q27106691
  • Mol file:28178-92-9.mol
Futoquinol

Synonyms:futoquinol

Suppliers and Price of Futoquinol
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
  • Crysdot
  • Futoquinol 95+%
  • 5mg
  • $ 730.00
  • Arctom
  • Futoquinol ≥98%
  • 5mg
  • $ 413.00
Total 11 raw suppliers
Chemical Property of Futoquinol
Chemical Property:
  • Vapor Pressure:1.03E-10mmHg at 25°C 
  • Boiling Point:515°Cat760mmHg 
  • Flash Point:225.6°C 
  • PSA:53.99000 
  • Density:1.2g/cm3 
  • LogP:3.81930 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:354.14672380
  • Heavy Atom Count:26
  • Complexity:659
Purity/Quality:

98%Min *data from raw suppliers

Futoquinol 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC
  • Isomeric SMILES:C/C(=C\C1=CC2=C(C=C1)OCO2)/C3(C=C(C(=O)C=C3OC)CC=C)OC
Technology Process of Futoquinol

There total 6 articles about Futoquinol 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 2,3-dicyano-5,6-dichloro-p-benzoquinone; In benzene; for 24h; Heating;
DOI:10.1016/S0040-4039(00)94967-0
Guidance literature:
Multi-step reaction with 5 steps
1: 93 percent / n-BuLi / tetrahydrofuran / 1 h / -70 - -20 °C
2: 78 percent / Raney Ni / dioxane / 20 h / Heating
3: 1.) K2CO3 / 1.) acetone, reflux, 11 h, 2.) 125 grad C, 4 h
4: 51 percent / tetrahydrofuran / electrolyzis, glassy carbon anode, platinum cathode
5: 72 percent / DDQ / benzene / 24 h / Heating
With n-butyllithium; nickel; potassium carbonate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; 1,4-dioxane; benzene;
DOI:10.1016/S0040-4039(00)94967-0
Guidance literature:
Multi-step reaction with 5 steps
1: 93 percent / n-BuLi / tetrahydrofuran / 1 h / -70 - -20 °C
2: 78 percent / Raney Ni / dioxane / 20 h / Heating
3: 1.) K2CO3 / 1.) acetone, reflux, 11 h, 2.) 125 grad C, 4 h
4: 51 percent / tetrahydrofuran / electrolyzis, glassy carbon anode, platinum cathode
5: 72 percent / DDQ / benzene / 24 h / Heating
With n-butyllithium; nickel; potassium carbonate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; 1,4-dioxane; benzene;
DOI:10.1016/S0040-4039(00)94967-0
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