1236046-54-0

Basic information

• Product Name: [1,1'-biphenyl]-4-yl(2-(pyridin-2-yl)phenyl)methanone
• Synonyms: [1,1'-biphenyl]-4-yl(2-(pyridin-2-yl)phenyl)methanone
• CAS NO: 1236046-54-0
• Molecular Weight: 335.405
• Mol File: 1236046-54-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: [1,1'-biphenyl]-4-yl(2-(pyridin-2-yl)phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1'-biphenyl]-4-yl(2-(pyridin-2-yl)phenyl)methanone(1236046-54-0)
• EPA Substance Registry System: [1,1'-biphenyl]-4-yl(2-(pyridin-2-yl)phenyl)methanone(1236046-54-0)

Safety Data

• Hazardous Substances Data: 1236046-54-0(Hazardous Substances Data)

Upstream product

• 1008-89-5 2-phenylpyridine 
• 5449-21-8 2-([1,1’-biphenyl]-4-yl)-2-oxoacetic acid 
• 98-80-6 phenylboronic acid 
• 109-04-6 2-bromo-pyridine 
• 92-91-1 biphenyl-4-acetaldehyde 
• 1404120-28-0 biphenyl-4-yl(2-(pyridin-2-yl)phenyl)methanol 
• 3218-36-8 4-Phenylbenzaldehyde 

Downstream Products

• 1245266-28-7 2-([1,1',4',1''-terphenyl]-2-yl)pyridine 

Relevant articles and documents

Acylation of Arenes with Aldehydes through Dual C-H Activations by Merging Photocatalysis and Palladium Catalysis

An acylation of arenes with aldehydes through dual C-H activations at room temperature is reported. The acylation was initiated by phenanthraquinone-catalyzed hydrogen atom transfer from aldehyde under visible light irradiation. The aldehyde-derived acyl

Silver catalyzed pyridine-directed acceptorless dehydrogenation of secondary alcohols

A silver catalyzed pyridine-directed acceptorless dehydrogenation of secondary benzyl alcohols was developed. This general procedure delivers ketones with high atom-economy and hydrogen was the sole byproduct. This dehydrogenation reaction has a good functional group tolerance and high efficiency (up to 90% yield and 10,000/1 substrates-to-catalyst ratio).

Decarboxylative acylation of arenes with α-oxocarboxylic acids via palladium-catalyzed C-H activation

(Equation Presented). An efficient palladium-catalyzed decarboxylative acylation of unactivated arenes with α-oxocarboxylic acids is reported. This method provides a novel access to aryl ketones.