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6,4'-DIBROMOFLAVONE

Base Information Edit
  • Chemical Name:6,4'-DIBROMOFLAVONE
  • CAS No.:213894-81-6
  • Molecular Formula:C15H8Br2O2
  • Molecular Weight:380.035
  • Hs Code.:
  • Mol file:213894-81-6.mol
6,4'-DIBROMOFLAVONE

Synonyms:6,4'-DIBROMOFLAVONE;

Suppliers and Price of 6,4'-DIBROMOFLAVONE
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
  • American Custom Chemicals Corporation
  • 6,4'-DIBROMOFLAVONE 95.00%
  • 100MG
  • $ 582.12
Total 1 raw suppliers
Chemical Property of 6,4'-DIBROMOFLAVONE Edit
Chemical Property:
  • Boiling Point:458.0±45.0 °C(Predicted) 
  • PSA:30.21000 
  • Density:1.795±0.06 g/cm3(Predicted) 
  • LogP:4.98500 
Purity/Quality:

6,4'-DIBROMOFLAVONE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 6,4'-DIBROMOFLAVONE

There total 5 articles about 6,4'-DIBROMOFLAVONE 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 sulfuric acid; at 20 ℃; for 1h;
Guidance literature:
With dipotassium peroxodisulfate; In water; 1,2-dichloro-ethane; at 100 ℃; for 2h; regioselective reaction; Sealed tube; Green chemistry;
DOI:10.1039/c7cc02107k
Guidance literature:
Multi-step reaction with 2 steps
1: 74.3 percent / KOH; pyridine / 1 h / 60 °C
2: 89.5 percent / sulfuric acid / 0.33 h / 20 °C
With pyridine; potassium hydroxide; sulfuric acid; 1: Baker-Venkataraman rearrangement;
DOI:10.1016/j.bmc.2004.12.006
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