80635-90-1

Upstream product

• 1008-89-5 2-phenylpyridine 
• 141-78-6 ethyl acetate 
• 3678-62-4 2-chloro-4-picoline 
• 3475-21-6 4-methyl-2-phenylpyridine 
• 74-88-4 methyl iodide 
• 98-80-6 phenylboronic acid 

Downstream Products

• 80635-50-3 4-Ethyl-6-phenyl-pyridine-2-carboxylic acid (1H-tetrazol-5-yl)-amide 
• 80636-10-8 4-Ethyl-6-phenyl-pyridine-2-carboxylic acid 

Relevant academic research and scientific papers

Visible-light- And bromide-mediated photoredox Minisci alkylation of N-heteroarenes with ester acetates

A visible-light-induced photoredox Minisci alkylation reaction of N-heteroarenes with ethyl acetate has been reported. The low-toxic ethyl acetate was used for the first time as an alkylation reagent. Hence, 4-quinazolinones, quinolines and pyridines reacted smoothly in the current reaction system. Mechanistic studies indicate that LiBr plays a key role to dramatically improve the efficiency of the reaction by the mediation of hydrogen atom transfer. This journal is

HETEROLEPTIC IRIDIUM COMPLEXES AS DOPANTS

Novel phosphorescent heteroleptic iridium complexes with phenylpyridine and dibenzo-containing ligands are provided. Alkyl substitution at specific positions on the ligands gives rise to compounds with improved OLED properties, including saturated green emission.

HETEROLEPTIC IRIDIUM COMPLEXES AS DOPANTS

Novel phosphorescent heteroleptic iridium complexes with phenylpyridine and dibenzo-containing ligands are provided. Alkyl substitution at specific positions on the ligands gives rise to compounds with improved OLED properties, including saturated green emission.