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Regorafenib Impurity 6

Base Information
  • Chemical Name:Regorafenib Impurity 6
  • CAS No.:1187945-05-6
  • Molecular Formula:C20H12ClF4N3O4
  • Molecular Weight:469.78
  • Hs Code.:
  • Mol file:1187945-05-6.mol
Regorafenib Impurity 6

Synonyms:4-(4-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido)-3-fluorophenoxy) picolinic acid

Suppliers and Price of Regorafenib Impurity 6
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
  • TRC
  • 4-(4-(3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido)-3-fluorophenoxy)picolinicAcid
  • 5mg
  • $ 80.00
Total 12 raw suppliers
Chemical Property of Regorafenib Impurity 6
Chemical Property:
  • Boiling Point:499.8±45.0 °C(Predicted) 
  • PKA:0.97±0.50(Predicted) 
  • Density:1.587±0.06 g/cm3(Predicted) 
Purity/Quality:

99%, *data from raw suppliers

4-(4-(3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido)-3-fluorophenoxy)picolinicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 4-(4-(3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido)-3-fluorophenoxy)picolinic Acid -- Regorafenib Impurity 6
Technology Process of Regorafenib Impurity 6

There total 7 articles about Regorafenib Impurity 6 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:
Multi-step reaction with 2 steps
1: dichloromethane / 16 h / 20 °C
2: trifluoroacetic acid; triethylsilane / dichloromethane / 16 h / 50 °C
With triethylsilane; trifluoroacetic acid; In dichloromethane;
Guidance literature:
Multi-step reaction with 5 steps
1.1: thionyl chloride; N,N-dimethyl-formamide / 2 h / Reflux
2.1: pyridine / dichloromethane / 16 h / -40 - 50 °C
3.1: potassium tert-butylate / N,N-dimethyl acetamide / 0.5 h / 20 °C
3.2: 1 h / 100 °C
4.1: dichloromethane / 16 h / 20 °C
5.1: trifluoroacetic acid; triethylsilane / dichloromethane / 16 h / 50 °C
With pyridine; triethylsilane; thionyl chloride; potassium tert-butylate; N,N-dimethyl-formamide; trifluoroacetic acid; In dichloromethane; N,N-dimethyl acetamide;
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