Application of 56-06-4, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 56-06-4, Name is 2,6-Diaminopyrimidin-4(1H)-one, SMILES is O=C1N=C(N)NC(N)=C1, belongs to pyrimidines compound. In a article, author is Mohamadpour, Farzaneh, introduce new discover of the category.
Catalyst-Free Three-Component Tandem Green Synthesis of Pyrano[2,3-d]Pyrimidine Scaffolds in Ethylene Glycol (E-G) as a Recyclable Reaction Medium
A green, efficient and convenient synthesis of pyrano[2,3-d]pyrimidine scaffolds has been developed via one-pot three-component reaction of aryl aldehyde derivatives, malononitrile with barbituric acid/1,3-dimethylbarbituric acid using ethylene glycol (E-G) as a solvent as well as catalyst. Eighteen pyrano[2,3-d]pyrimidine scaffolds were selected for the library validation. The superiority of this method is environmental safety, catalyst-free, operational simplicity, metal-free, high yields, excellent functional group tolerance, easy workup procedure, less reaction time and the green ethylene glycol can be recovered and reused several times without any loss of efficiency.
Application of 56-06-4, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 56-06-4 is helpful to your research.
Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia