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6,8,11-Trihydroxy-3-methoxy-1-methyl-10H-benzo[b]xanthene-7,10,12-trione

Base Information
  • Chemical Name:6,8,11-Trihydroxy-3-methoxy-1-methyl-10H-benzo[b]xanthene-7,10,12-trione
  • CAS No.:33390-22-6
  • Molecular Formula:C19H12O8
  • Molecular Weight:0
  • Hs Code.:2932999099
  • Mol file:33390-22-6.mol
6,8,11-Trihydroxy-3-methoxy-1-methyl-10H-benzo[b]xanthene-7,10,12-trione

Synonyms:Norbikaverin;6,8,11-trihydroxy-3-methoxy-1-methyl-benzo[b]xanthene-7,10,12-trione;

Suppliers and Price of 6,8,11-Trihydroxy-3-methoxy-1-methyl-10H-benzo[b]xanthene-7,10,12-trione
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 3 raw suppliers
Chemical Property of 6,8,11-Trihydroxy-3-methoxy-1-methyl-10H-benzo[b]xanthene-7,10,12-trione
Chemical Property:
  • PSA:134.27000 
  • LogP:2.49530 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 6,8,11-Trihydroxy-3-methoxy-1-methyl-10H-benzo[b]xanthene-7,10,12-trione

There total 17 articles about 6,8,11-Trihydroxy-3-methoxy-1-methyl-10H-benzo[b]xanthene-7,10,12-trione 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 manganese(IV) oxide; sulfuric acid; at 60 ℃; for 0.5h;
DOI:10.1039/P19810002710
Guidance literature:
Multi-step reaction with 2 steps
1: 65 percent / potassium dichromate / dioxane; acetic acid / 5 h / Ambient temperature
2: 28 percent / MnO2, H2SO4 (conc.) / 0.5 h / 60 °C
With potassium dichromate; manganese(IV) oxide; sulfuric acid; In 1,4-dioxane; acetic acid;
DOI:10.1039/P19810002710
Guidance literature:
Multi-step reaction with 12 steps
1: K2CO3 / acetone / 72 h / Heating
2: NaOH / ethanol / 1.5 h / Heating
3: thionyl chloride / benzene / 1 h / Heating
4: Et3N / diethyl ether / 4 h
5: 86 percent / silver benzoate, Et3N / 1 h / Heating
6: 55 percent / AcOH, perchloric acid (3 drops) / 0.25 h / Ambient temperature
7: NaH / tetrahydrofuran / 2 h / Ambient temperature
8: tetrahydrofuran / 0.5 h
9: 27 percent / ethanol / 1 h / Irradiation
10: 9 percent / KOH (40percent) / ethanol; dioxane / 2.5 h / Heating
11: 65 percent / potassium dichromate / dioxane; acetic acid / 5 h / Ambient temperature
12: 28 percent / MnO2, H2SO4 (conc.) / 0.5 h / 60 °C
With potassium dichromate; manganese(IV) oxide; potassium hydroxide; sodium hydroxide; thionyl chloride; perchloric acid; sulfuric acid; silver benzoate; sodium hydride; potassium carbonate; acetic acid; triethylamine; In tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; acetic acid; acetone; benzene;
DOI:10.1039/P19810002710
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