1416802-91-9

Basic information

• Product Name: 2',6'-diphenyl-2,4'-bipyridine
• Synonyms: 2',6'-diphenyl-2,4'-bipyridine
• CAS NO: 1416802-91-9
• Molecular Weight: 308.382
• Mol File: 1416802-91-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2',6'-diphenyl-2,4'-bipyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2',6'-diphenyl-2,4'-bipyridine(1416802-91-9)
• EPA Substance Registry System: 2',6'-diphenyl-2,4'-bipyridine(1416802-91-9)

Safety Data

• Hazardous Substances Data: 1416802-91-9(Hazardous Substances Data)

Upstream product

• 1479-22-7 ethyl 2-fluoro-3-oxo-3-phenylpropionate 
• 5337-53-1 3-phenyl-1-(2-pyridyl)prop-2-en-1-one 
• 109-06-8 α-picoline 
• 98-86-2 acetophenone 
• 5029-67-4 2-iodopyridine 
• 1426150-35-7 C₁₇H₁₅N 
• 3731-51-9 2-(Aminomethyl)pyridine 
• 122712-52-1 phenyl-1 amino-1 butadiene-2,3 
• 100-52-7 benzaldehyde 

Relevant articles and documents

Copper(II) supported on magnetic chitosan: A green nanocatalyst for the synthesis of 2,4,6-triaryl pyridines by C-N bond cleavage of benzylamines

In this paper, Cu/magnetic chitosan has been synthesized and used as a new green nanocatalyst for highly efficient synthesis of 2,4,6-triaryl pyridines via C-N bond cleavage of benzylamines under aerobic oxidation at 90 °C. The chemical and structural properties of the synthesized catalyst were determined by scanning electron microscopy, energy-dispersive X-ray, X-ray powder diffraction, thermogravimetric analysis and flame atomic absorption spectroscopies. It is found that the catalyst can be easily separated from the reaction mixture by an external magnetic field and recycled several times without a significant loss in activity.

One-Pot Reactions for Modular Synthesis of Polysubstituted and Fused Pyridines

A 2-fluoro-1,3-dicarbonyl-initiated one-pot Michael addition/[5 + 1] annulation/dehydrofluorinative aromatization reaction sequence is introduced for regioselective synthesis of di-, tri-, tetra-, and pentasubstituted pyridines as well as fused pyridines. This simple and modular synthesis is performed using readily available starting materials and under transition-metal catalyst-free conditions.