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2,2'-BIPYRIDINE-4,4'-DICARBONITRILE

Base Information Edit
  • Chemical Name:2,2'-BIPYRIDINE-4,4'-DICARBONITRILE
  • CAS No.:727380-18-9
  • Molecular Formula:C12H14N4
  • Molecular Weight:214.27
  • Hs Code.:
  • Mol file:727380-18-9.mol
2,2'-BIPYRIDINE-4,4'-DICARBONITRILE

Synonyms:4,4'-bis(aminomethyl)-2,2'-bipyridine

Suppliers and Price of 2,2'-BIPYRIDINE-4,4'-DICARBONITRILE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 11 raw suppliers
Chemical Property of 2,2'-BIPYRIDINE-4,4'-DICARBONITRILE Edit
Chemical Property:
Purity/Quality:

99.0% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
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MSDS Files:
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Technology Process of 2,2'-BIPYRIDINE-4,4'-DICARBONITRILE

There total 6 articles about 2,2'-BIPYRIDINE-4,4'-DICARBONITRILE 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:
4,4'-bis(bromomethyl)-2,2'-bipyridine; With potassium phtalimide; In N,N-dimethyl-formamide;
With hydrazine hydrate; In ethanol;
DOI:10.1016/j.tetasy.2013.03.014
Guidance literature:
With palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; for 48h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 5 steps
1: potassium permanganate; sulfuric acid / 24 h / Reflux
2: sulfuric acid / Reflux
3: sodium tetrahydroborate / ethanol / Reflux
4: hydrogen bromide / Reflux
5: potassium phtalimide / N,N-dimethyl-formamide
With sodium tetrahydroborate; potassium permanganate; sulfuric acid; hydrogen bromide; potassium phtalimide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tetasy.2013.03.014
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