Chemical Research Letters, May 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. Application In Synthesis of 3,3′,3”-(1,3,5-Triazinane-1,3,5-triyl)tris(N,N-dimethylpropan-1-amine),15875-13-5, Name is 3,3′,3”-(1,3,5-Triazinane-1,3,5-triyl)tris(N,N-dimethylpropan-1-amine), SMILES is CN(C)CCCN1CN(CCCN(C)C)CN(CCCN(C)C)C1, belongs to pyrrolines compound. In a document, author is Gein, V. L., introduce the new discover.
Synthesis and Some Transformations of 5-Aryl-4-(4-halogenaroyl)-3-hydroxy-1-cyanomethyl-3-pyrrolin-2-ones
5-Aryl-4-aroyl-3-hydroxy-1-cyanomethyl-3-pyrrolin-2-ones were synthesized by a three-component reaction of aroylpyruvic acid methyl ester with a mixture of aromatic aldehyde and 2-aminoacetonitrile sulfate in glacial acetic acid in the presence of anhydrous sodium acetate. The possibility of their reactions with p-toluidine and hydrazine hydrate was shown.
The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates. Interested yet? Read on for other articles about 15875-13-5. Application In Synthesis of 3,3′,3”-(1,3,5-Triazinane-1,3,5-triyl)tris(N,N-dimethylpropan-1-amine).
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem