128733-91-5

Upstream product

• 128733-90-4 (2-hydroxy-5-methylphenacyl)pyridinium chloride 
• 38373-80-7 3-dimethylamino-1-(2-hydroxy-5-methylphenyl)propan-1-one hydrochloride 
• 110-86-1 pyridine 
• 22307-94-4 2-chloroacetyl-4-methylphenol 
• 626-05-1 2,6-Dibromopyridine 
• 1450-72-2 5-methyl-2-hydroxyacetophenone 
• 70548-79-7 2-methoxy-5-methylphenyl magnesium bromide 

Downstream Products

• 1233923-43-7 C₁₂H₈NC₆H₄B(OC₆H₃(CH₃))2C₅H₃N 
• 877991-72-5 1,6-bis(2-hydroxy-5-methylphenyl)pyridyl boron 2-methoxylbenzene 
• 128733-93-7 2,6-bis<3-(hydroxymethyl)-2-methoxy-5-methylphenyl>-pyridine N-oxide 
• 108294-03-7 2,6-bis<3-(hydroxymethyl)-2-methoxy-5-methylphenyl>-pyridine 
• 128733-92-6 2,6-bis<2-hydroxy-3-(hydroxymethyl)-5-methylphenyl>-pyridine 

Relevant academic research and scientific papers

Highly efficient white organic electroluminescence from a double-layer device based on a boron hydroxyphenylpyridine complex

Electroluminescence from 400 to 700 nm (see right picture) is exhibited by an organic electroluminescent device based on (mdppy) BF (left picture) as emitter and a, 1,1′-biphenyl-4,4′-diamine derivative as a hole-transporting material.The device emits whi

Host-Guest Complexation. 53.) Functional Groups Preorganized in Hemispherands for Binding Alkali Metal and Ammonium Cations

The synthesis and free energies are reported for 10 new hemispherands (1, 2, 4, 6, 7-9, 11-13) binding alkali metal and ammonium picrate salts at 25 deg C in CDCl3 saturated with D2O.These hemispherands possess the general structure I, in which two 4-subs