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(E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine

Base Information Edit
  • Chemical Name:(E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine
  • CAS No.:1185855-70-2
  • Molecular Formula:C18H19N5O2
  • Molecular Weight:337.381
  • Hs Code.:
  • Mol file:1185855-70-2.mol
(E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine

Synonyms:(E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine Edit
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Technology Process of (E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine

There total 16 articles about (E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine 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 hydroxylamine; In ethanol; water; at 20 ℃; for 12h;
Guidance literature:
Multi-step reaction with 7 steps
1.1: water; potassium hydroxide / methanol / 14 h / Reflux
2.1: hydrogenchloride / 1,4-dioxane / 14 h / Reflux
2.2: pH > 12
3.1: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C
4.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 100 °C
5.1: tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine / 1,4-dioxane; toluene / 0.17 h / 150 °C / Microwave irradiation
6.1: potassium acetate / methanol / 0 - 20 °C
7.1: hydroxylamine / ethanol; water / 12 h / 20 °C
With hydrogenchloride; water; hydrogen; hydroxylamine; potassium acetate; potassium carbonate; potassium hydroxide; tris-(dibenzylideneacetone)dipalladium(0); palladium 10% on activated carbon; triphenylphosphine; In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 4 steps
1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 100 °C
2: tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine / 1,4-dioxane; toluene / 0.17 h / 150 °C / Microwave irradiation
3: potassium acetate / methanol / 0 - 20 °C
4: hydroxylamine / ethanol; water / 12 h / 20 °C
With hydroxylamine; potassium acetate; potassium carbonate; tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine; In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide; toluene;
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