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cabozantinib-N-oxide

Base Information Edit
  • Chemical Name:cabozantinib-N-oxide
  • CAS No.:1621681-63-7
  • Molecular Formula:C28H24FN3O6
  • Molecular Weight:517.513
  • Hs Code.:
  • Mol file:1621681-63-7.mol
cabozantinib-N-oxide

Synonyms:

Suppliers and Price of cabozantinib-N-oxide
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
  • TRC
  • CabozantinibN-oxide
  • 10mg
  • $ 545.00
Total 5 raw suppliers
Chemical Property of cabozantinib-N-oxide Edit
Chemical Property:
Purity/Quality:

95% *data from raw suppliers

CabozantinibN-oxide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Cabozantinib N-oxide is a impurity of Cabozantinib (X745500), a medication used to treat medullary thyroid cancer. As well, it can be used in biological study. Computational network biological approach based on pathway cross-talk inhibition identified new synergistic drug combinations using raloxifene and cabozantinib for treatment of human breast cancer in xenograft mouse model. Potent c-MET inhibitor.
Technology Process of cabozantinib-N-oxide

There total 6 articles about cabozantinib-N-oxide 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:
((4-fluorophenyl)carbamoyl)cyclopropanecarboxylic acid; With 6-chloro-3-((dimethylamino)(dimethyliminio)methyl)-1H-benzo[d][1,2,3]triazol-3-ium-1-olatehexafluorophosphate(V); N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;
C17H16N2O4; In N,N-dimethyl-formamide; at 35 ℃; for 3h;
Guidance literature:
With sodium peroxoborate tetrahydrate; acetic acid; at 65 ℃;
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / ethyl acetate / 1 h / 0 - 10 °C / Large scale
1.2: 1 h / 10 °C / Large scale
2.1: ethyl acetate / 16 h / 10 °C / Large scale
3.1: 6-chloro-3-((dimethylamino)(dimethyliminio)methyl)-1H-benzo[d][1,2,3]triazol-3-ium-1-olatehexafluorophosphate(V); N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C
3.2: 3 h / 35 °C
With 6-chloro-3-((dimethylamino)(dimethyliminio)methyl)-1H-benzo[d][1,2,3]triazol-3-ium-1-olatehexafluorophosphate(V); triethylamine; N-ethyl-N,N-diisopropylamine; In ethyl acetate; N,N-dimethyl-formamide;
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