5216-04-6

Basic information

• Product Name: 3,4-DIPHENYLPYRIDINE
• Synonyms: 3,4-DIPHENYLPYRIDINE
• CAS NO: 5216-04-6
• Molecular Formula: C₁₇H₁₃N
• Molecular Weight: 231.29
• Mol File: 5216-04-6.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 345.3 °C at 760 mmHg
• Flash Point: 147.4 °C
• Appearance: /
• Density: 1.084 g/cm³
• Vapor Pressure: 0.000124mmHg at 25°C
• Refractive Index: 1.605
• CAS DataBase Reference: 3,4-DIPHENYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIPHENYLPYRIDINE(5216-04-6)
• EPA Substance Registry System: 3,4-DIPHENYLPYRIDINE(5216-04-6)

Safety Data

• Hazardous Substances Data: 5216-04-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H13N/c1-3-7-14(8-4-1)16-11-12-18-13-17(16)15-9-5-2-6-10-15/h1-13H

Upstream product

• 110567-95-8 2-chloro-4,5-diphenylpyridine 
• 1219711-46-2 C₁₂H₁₁NO₃S 
• 98-80-6 phenylboronic acid 
• 104-55-2 3-phenyl-propenal 
• 122-78-1 phenylacetaldehyde 
• 137845-37-5 4-methyl-N-(3-phenylallylidene)benzenesulfonamide 
• 1379538-77-8 C₂₂H₂₃NO₂ 
• 110567-84-5 2,6-diphenyl-2,3-dihydro-4H-thiopyran-4-one O-tosyloxime 
• 110567-92-5 2,7-diphenyl-5-oxo-2,3,4,5-tetrahydro-1,4-thiazepine 1-oxide 
• 110567-82-3 2,6-diphenyl-2,3-dihydro-4H-thiopyran-4-one oxime 
• 110567-93-6 2-acetoxy-4,5-diphenylpiridine 
• 110567-87-8 2,7-diphenyl-5-oxo-2,3,4,5-tetrahydro-1,4-thiazepine 
• 110567-94-7 4,5-diphenyl-2-pyridone 
• 936629-99-1 1-(4-methylphenylsulfonyl)-4,5-diphenyl-1,2,5,6-tetrahydropyridine 

Relevant articles and documents

Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes

A new efficient synthetic route to unsymmetrically substituted dihydropyridine scaffolds via dehydrative [4 + 2] cycloaddition of N-tosylated α,β-unsaturated imines with aldehydes has been developed. This transformation is enabled by (i) the remarkable ca

De novo synthesis of 1,4-dihydropyridines and pyridines

An efficient and general method for the synthesis of 1,4-dihydropyridines and pyridines based on a lithiation/isomerization/intramolecular carbolithiation sequence is reported. This procedure provides an efficient, divergent, and straightforward entry to a wide range of polysubstituted dihydropyridines and pyridines starting from readily available N-allyl-ynamides.

Selenium dioxide-mediated methoxyhydroxylation of cyclic arylolefin

Selenium dioxide-mediated methoxyhydroxylation of cyclic arylolefin with the modest yields is described. This facile strategy was also used to synthesize several 4-arylpyridines, 3-hydroxy-4-arylpyridines, and 3,4-diarylpyridines. Crown Copyright