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Betuletol

Base Information
  • Chemical Name:Betuletol
  • CAS No.:35214-88-1
  • Molecular Formula:C17H14 O7
  • Molecular Weight:330.294
  • Hs Code.:
  • NSC Number:641548
  • DSSTox Substance ID:DTXSID70420059
  • Nikkaji Number:J487.482J
  • Wikidata:Q82231318
  • Metabolomics Workbench ID:25954
  • ChEMBL ID:CHEMBL311155
  • Mol file:35214-88-1.mol
Betuletol

Synonyms:Betuletol;NSC641548;6,4'-Dimethoxy-3,5,7-trihydroxyflavone;35214-88-1;Beturetol;Oprea1_748279;CHEMBL311155;DTXSID70420059;LMPK12112871;NSC-641548;NCI60_014067

Suppliers and Price of Betuletol
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 2 raw suppliers
Chemical Property of Betuletol
Chemical Property:
  • Vapor Pressure:9.54E-15mmHg at 25°C 
  • Boiling Point:589.6°Cat760mmHg 
  • Flash Point:220.4°C 
  • Density:1.507g/cm3 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:330.07395278
  • Heavy Atom Count:24
  • Complexity:509
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)O
Technology Process of Betuletol

There total 14 articles about Betuletol 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 hydrogen; palladium on activated charcoal; In methanol; ethyl acetate; Ambient temperature;
DOI:10.1248/cpb.45.446
Guidance literature:
Multi-step reaction with 11 steps
1: 100 percent / conc. HCl, acetic acid / 1 h / Ambient temperature
2: 83 percent / K2CO3, KI / acetone; dimethylformamide / Heating
3: 75 percent / AlBr3, NaI / acetonitrile / 0.25 h / 0 °C
4: pyridine / 2 h / 70 - 80 °C
5: KOH / pyridine / 80 °C
6: 87 percent / conc. H2SO4, acetic acid / 1 h / 50 °C
7: 71 percent / dimethyldioxirane / acetone / 0 °C
8: 96 percent / K2CO3 / acetone / Heating
9: 91 percent / AlCl3 / acetonitrile / 0.5 h / Ambient temperature
10: 90 percent / K2CO3 / methanol / 1.5 h / Heating
11: 90 percent / H2 / 10percent Pd/C / methanol; ethyl acetate / Ambient temperature
With pyridine; hydrogenchloride; potassium hydroxide; aluminium trichloride; aluminum tri-bromide; sulfuric acid; hydrogen; 3,3-dimethyldioxirane; potassium carbonate; acetic acid; potassium iodide; sodium iodide; palladium on activated charcoal; In pyridine; methanol; ethyl acetate; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1248/cpb.45.446
Guidance literature:
Multi-step reaction with 10 steps
1: 83 percent / K2CO3, KI / acetone; dimethylformamide / Heating
2: 75 percent / AlBr3, NaI / acetonitrile / 0.25 h / 0 °C
3: pyridine / 2 h / 70 - 80 °C
4: KOH / pyridine / 80 °C
5: 87 percent / conc. H2SO4, acetic acid / 1 h / 50 °C
6: 71 percent / dimethyldioxirane / acetone / 0 °C
7: 96 percent / K2CO3 / acetone / Heating
8: 91 percent / AlCl3 / acetonitrile / 0.5 h / Ambient temperature
9: 90 percent / K2CO3 / methanol / 1.5 h / Heating
10: 90 percent / H2 / 10percent Pd/C / methanol; ethyl acetate / Ambient temperature
With pyridine; potassium hydroxide; aluminium trichloride; aluminum tri-bromide; sulfuric acid; hydrogen; 3,3-dimethyldioxirane; potassium carbonate; acetic acid; potassium iodide; sodium iodide; palladium on activated charcoal; In pyridine; methanol; ethyl acetate; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1248/cpb.45.446
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