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3''-CHLOROCHALCONE

Base Information Edit
  • Chemical Name:3''-CHLOROCHALCONE
  • CAS No.:20426-48-6
  • Molecular Formula:C15H11ClO
  • Molecular Weight:242.705
  • Hs Code.:2914700090
  • Mol file:20426-48-6.mol
3''-CHLOROCHALCONE

Synonyms:2-Propen-1-one, 1-(3-chlorophenyl)-3-phenyl-;3'-Chlor-chalcon;6-chloro-2-phenyl-4H-chromen-4-one;3'-CHLOROCHALCONE;

Suppliers and Price of 3''-CHLOROCHALCONE
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
  • Sigma-Aldrich
  • 3'-CHLOROCHALCONE Aldrich
  • 250mg
  • $ 55.10
  • American Custom Chemicals Corporation
  • 3'-CHLOROCHALCONE 95.00%
  • 1G
  • $ 754.95
Total 2 raw suppliers
Chemical Property of 3''-CHLOROCHALCONE Edit
Chemical Property:
  • Melting Point:93 °C 
  • Boiling Point:388.2±42.0 °C(Predicted) 
  • PSA:17.07000 
  • Density:1.202±0.06 g/cm3(Predicted) 
  • LogP:4.23610 
Purity/Quality:

99% *data from raw suppliers

3'-CHLOROCHALCONE Aldrich *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 3''-CHLOROCHALCONE

There total 7 articles about 3''-CHLOROCHALCONE 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 sodium hydroxide; In ethanol; water; for 4h; Cooling with ice;
DOI:10.1002/bkcs.11749
Guidance literature:
With potassium hydroxide; In ethanol; water; at 25 ℃;
DOI:10.1002/bkcs.11813
Guidance literature:
With Hβ zeolite; In water; at 100 ℃; for 20h; Sealed tube;
DOI:10.1039/c6ra11593d
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