114544-17-1

Upstream product

• 99-91-2 para-chloroacetophenone 
• 84922-30-5 [1-(4-Chloro-phenyl)-meth-(E)-ylidene]-quinolin-6-yl-amine 
• 580-15-4 6-aminoquinoline 
• 104-88-1 4-chlorobenzaldehyde 

Relevant academic research and scientific papers

SPECTRAL-LUMINISCENCE CHARACTERISTICS OF 1,3-DIARYL-4,7-PHENANTHROLINES

The effect of the nature of the substituents and the solvent on the absorption and fluorescence spectra and the fluorescence quantum yields of 1,3-diaryl-4,7-phenanthrolines was studied.Electron-donor groups in the para position of the phenyl ring cause a

Synthesis of new haloderivatives of benzo[f]quinoline and 4,7-phenanthroline

By condensations of 2-naphthylamine and 6-aminoquinoline with halogen-substituted benzaldehydes, 3-acetylpyridine and acetophenone derivatives new 1,3-diaryl(heteryl)benzo-[f]quinolines and 4,7-phenanthrolines were synthesized containing atoms of fluorine, bromine, and chlorine in the phenyl rings.