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2-[4-({5-[(2,6-difluoro-3,5-dimethoxybenzyl)oxy]pyrimidin-2-yl}amino)phenoxy]-2-methylpropionic acid

Base Information Edit
  • Chemical Name:2-[4-({5-[(2,6-difluoro-3,5-dimethoxybenzyl)oxy]pyrimidin-2-yl}amino)phenoxy]-2-methylpropionic acid
  • CAS No.:1453211-13-6
  • Molecular Formula:C23H23F2N3O6
  • Molecular Weight:475.449
  • Hs Code.:
  • Mol file:1453211-13-6.mol
2-[4-({5-[(2,6-difluoro-3,5-dimethoxybenzyl)oxy]pyrimidin-2-yl}amino)phenoxy]-2-methylpropionic acid

Synonyms:2-[4-({5-[(2,6-difluoro-3,5-dimethoxybenzyl)oxy]pyrimidin-2-yl}amino)phenoxy]-2-methylpropionic acid

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Chemical Property of 2-[4-({5-[(2,6-difluoro-3,5-dimethoxybenzyl)oxy]pyrimidin-2-yl}amino)phenoxy]-2-methylpropionic acid Edit
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Technology Process of 2-[4-({5-[(2,6-difluoro-3,5-dimethoxybenzyl)oxy]pyrimidin-2-yl}amino)phenoxy]-2-methylpropionic acid

There total 5 articles about 2-[4-({5-[(2,6-difluoro-3,5-dimethoxybenzyl)oxy]pyrimidin-2-yl}amino)phenoxy]-2-methylpropionic acid 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 palladium(II) acetate-2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1'-biphenyl; caesium carbonate; In tert-butyl alcohol; at 120 ℃; Inert atmosphere;
Guidance literature:
Multi-step reaction with 3 steps
1: triethylamine / tetrahydrofuran / 1 h / Cooling with ice
2: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C
3: caesium carbonate; palladium(II) acetate-2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1'-biphenyl / tert-butyl alcohol / 120 °C / Inert atmosphere
With palladium(II) acetate-2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1'-biphenyl; potassium carbonate; caesium carbonate; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide; tert-butyl alcohol;
Guidance literature:
Multi-step reaction with 5 steps
1: Selectfluor / acetonitrile / 20 °C / Cooling with ice
2: lithium borohydride / tetrahydrofuran / 87 h / 20 °C / Cooling with ice
3: triethylamine / tetrahydrofuran / 1 h / Cooling with ice
4: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C
5: caesium carbonate; palladium(II) acetate-2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1'-biphenyl / tert-butyl alcohol / 120 °C / Inert atmosphere
With lithium borohydride; palladium(II) acetate-2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1'-biphenyl; potassium carbonate; caesium carbonate; Selectfluor; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
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