82299-14-7

Upstream product

• 88785-69-7 Phenyl-[1-pyridin-4-yl-meth-(Z)-ylidene]-amine 
• 586-95-8 pyridine-4-methanol 
• 62-53-3 aniline 

Downstream Products

• 88785-69-7 Phenyl-[1-pyridin-4-yl-meth-(Z)-ylidene]-amine 
• 3034-32-0 N-((pyridin-4-yl)methyl)benzenamine 
• 148336-19-0 4-methyl-2-(pyridin-4-yl)quinoline 
• 943858-21-7 4-(2-methylprop-1-enyl)-2-(4-pyridinyl)quinoline 
• 943858-27-3 C₁₉H₂₀N₂O 
• 97383-66-9 Phenylamino-pyridin-4-yl-acetonitrile 
• 159110-63-1 N-phenyl-N-[1-(pyridin-4-yl)but-3-enyl]amine 
• 52089-02-8 2-(pyridin-4-yl)quinoline 

Relevant academic research and scientific papers

Heterogeneously catalyzed one-pot synthesis of aldimines from primary alcohols and amines by supported ruthenium hydroxides

The one-pot synthesis of aldimines from primary alcohols and amines via sequential reactions of alcohol oxidation and dehydrative condensation could efficiently be promoted by supported ruthenium hydroxide catalysts, in particular Ru(OH)x/TiO2. The observed catalysis was truly heterogeneous and the retrieved catalyst could be reused without an appreciable loss of high catalytic performance. Copyright

193. Photoformation of (Z)-Isomers in Diarylazomethines. Part IV. Direct and Sensitized Photoisomerization of Pyridyl Analogues of Benzylidene-aniline and Absorption Spectra of their (Z)-Isomers

UV irradiation of solutions of the (E)-isomers of five (out of the possible six) monopyridyl analogues at reduced temperatures results in extensive (80-90percent) conversion into the corresponding (Z)-isomers.The process is reversible both thermally and photochemically.The (Z)-isomers are stable at temperatures below -80 deg, and their absorption spectra were estimated.Biacetyl-photosensitized (E)->(Z) isomerization was observed, with (Z)-contents of ca. 70percent at the photostationary state.