161121-63-7

Upstream product

• 3558-65-4 4-(4-methylphenyl)-2,6-diphenylpyridine 
• 104-87-0 4-methyl-benzaldehyde 
• 130317-99-6 1,5-diphenyl-3-(p-methylphenyl)-1,5-pentanedione 
• 4224-87-7 4-methyl-chalcone 
• 98-86-2 acetophenone 

Downstream Products

• 499201-95-5 2,6-diphenyl-4-(p-acetoxymethylphenyl)pyridine 
• 97419-28-8 4-(2,6-diphenylpyridin-4-yl)benzaldehyde 
• 499201-96-6 2,6-diphenyl-4-(p-hydroxymethylphenyl)pyridine 
• 1374853-89-0 4-(4-(azidomethyl)phenyl)-2,6-diphenylpyridine 

Relevant academic research and scientific papers

Aromatic ring-triarylpyridine compound as well as preparation method and application thereof

The invention discloses a synthesis method of an aromatic ring-triarylpyridine compound. A triarylpyridine framework and arylboronic acid are taken as substrates, a series of aromatic ring-triarylpyridine compounds are synthesized under the synergistic ef

Phenothiazine-triarylpyridine organic yellow-green emissive compound as well as preparation and application thereof

The invention discloses a novel phenothiazine-triarylpyridine organic yellow-green emissive compounds as well as preparation and application thereof. Phenothiazine serves as an electron donor (D), vinyl serves as a Pi electron bridge, 2,4,6-triarylpyridin

Triarylpyridine derivatives containing carbazole frameworks and preparation method and application thereof

The invention relates to triarylpyridine derivatives containing carbazole frameworks and a preparation method and application thereof. Through Witting-Horner and Suzuki coupling reaction, six D-pi-A molecules based on carbazole and 2, 4, 6-triarylpyridine

Spectral studies of multi-branched fluorescence dyes based on triphenylpyridine core

A series of novel triphenylpyridine-containing triphenylamine derivatives have been carefully designed and prepared in good yields using the stepwise route reactions. The relationship of photoluminescence property and structure of compounds 9-13 was syste

Influence of molecular weight on the aggregation-induced emission enhancement and spectral stability of vinyl polymers containing the fluorescent 2,4,6-triphenylpyridine pendant groups

The effect of molecular weight on the aggregation-induced emission enhancement (AIEE) and the spectral stability of vinyl polymers containing fluorescent 2,4,6-triphenylpyridine (TP) pendant groups was evaluated in this study. The high and low molecular w

Free radicals: XXVII. Synthesis of 2,6-diphenyl-4-[p-(2,6-diphenyl-4-pyridyl)phenyl]pyranyl

Starting with 2,6-diphenyl-4-(p-tolyl)pyridine a synthesis of 2,6-diphenyl-4-[p-(2,6-diphenyl-4-pyridyl)phenyl]pyrylium perchlorate was performed. By reduction of the latter the corresponding radical was obtained. The radical was shown to be unstable with respect to oxygen.