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Quinoline, 2-methyl-5-[2-[4-[[3-(4-morpholinyl)phenyl]methyl]-1-piperidinyl]ethoxy]-

Base Information
  • Chemical Name:Quinoline, 2-methyl-5-[2-[4-[[3-(4-morpholinyl)phenyl]methyl]-1-piperidinyl]ethoxy]-
  • CAS No.:586412-10-4
  • Molecular Formula:C28H35N3O2
  • Molecular Weight:445.605
  • Hs Code.:
Quinoline,
2-methyl-5-[2-[4-[[3-(4-morpholinyl)phenyl]methyl]-1-piperidinyl]ethoxy]-

Synonyms:

Suppliers and Price of Quinoline, 2-methyl-5-[2-[4-[[3-(4-morpholinyl)phenyl]methyl]-1-piperidinyl]ethoxy]-
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Quinoline, 2-methyl-5-[2-[4-[[3-(4-morpholinyl)phenyl]methyl]-1-piperidinyl]ethoxy]-
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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Technology Process of Quinoline, 2-methyl-5-[2-[4-[[3-(4-morpholinyl)phenyl]methyl]-1-piperidinyl]ethoxy]-

There total 6 articles about Quinoline, 2-methyl-5-[2-[4-[[3-(4-morpholinyl)phenyl]methyl]-1-piperidinyl]ethoxy]- 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 10% palladium on activated carbon; hydrogen; In ethanol; at 20 ℃; for 24h;
DOI:10.1016/j.bmcl.2008.11.052
Guidance literature:
Multi-step reaction with 2 steps
1: palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / 1,4-dioxane / Reflux
2: 10% palladium on activated carbon; hydrogen / ethanol / 24 h / 20 °C
With 10% palladium on activated carbon; hydrogen; palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In 1,4-dioxane; ethanol;
DOI:10.1016/j.bmcl.2008.11.052
Guidance literature:
Multi-step reaction with 4 steps
1: hydrogenchloride / diethyl ether / 72 h / 20 °C
2: potassium carbonate / N,N-dimethyl-formamide / 16 h / 100 °C
3: palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / 1,4-dioxane / Reflux
4: 10% palladium on activated carbon; hydrogen / ethanol / 24 h / 20 °C
With hydrogenchloride; 10% palladium on activated carbon; hydrogen; palladium diacetate; potassium carbonate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In 1,4-dioxane; diethyl ether; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2008.11.052
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