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Ivacaftor-d18

Base Information
  • Chemical Name:Ivacaftor-d18
  • CAS No.:1413431-05-6
  • Molecular Formula:C24H28N2O3
  • Molecular Weight:410.355
  • Hs Code.:
  • Mol file:1413431-05-6.mol
Ivacaftor-d18

Synonyms:N-(2,4-bis(1,1,1,3,3,3-d6-2-(methyl-d3)propan-2-yl)-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide

Suppliers and Price of Ivacaftor-d18
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
  • Usbiological
  • Ivacaftor-d18
  • 2.5mg
  • $ 460.00
Total 9 raw suppliers
Chemical Property of Ivacaftor-d18
Chemical Property:
Purity/Quality:

95% by HPLC; 95% atom D *data from raw suppliers

Ivacaftor-d18 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Ivacaftor-d18 is used in the treatment of cystic fibrosis. Ivacaftor is used in the treatment of cystic fibrosis. This is the labeled analog.
Technology Process of Ivacaftor-d18

There total 6 articles about Ivacaftor-d18 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 N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 3h;
Guidance literature:
Multi-step reaction with 5 steps
1.1: dmap; triethylamine / dichloromethane / 15 h / 0 - 20 °C
2.1: sulfuric acid; nitric acid / 2 h / 20 °C
2.2: 2 h / 20 °C
3.1: ammonium formate; palladium 10% on activated carbon / ethanol / 2 h / Reflux
4.1: hydrogenchloride / isopropyl alcohol / 15 h / 20 °C
5.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 3 h / 20 °C
With hydrogenchloride; dmap; sulfuric acid; palladium 10% on activated carbon; nitric acid; ammonium formate; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;
Guidance literature:
Multi-step reaction with 6 steps
1.1: sulfuric acid-d2 / dichloromethane / 15 h / 20 °C
2.1: dmap; triethylamine / dichloromethane / 15 h / 0 - 20 °C
3.1: sulfuric acid; nitric acid / 2 h / 20 °C
3.2: 2 h / 20 °C
4.1: ammonium formate; palladium 10% on activated carbon / ethanol / 2 h / Reflux
5.1: hydrogenchloride / isopropyl alcohol / 15 h / 20 °C
6.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 3 h / 20 °C
With hydrogenchloride; dmap; sulfuric acid; palladium 10% on activated carbon; nitric acid; ammonium formate; sulfuric acid-d2; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;
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