3558-65-4

Basic information

• Product Name: Pyridine, 4-(4-methylphenyl)-2,6-diphenyl-
• Synonyms: 2,6-diphenyl-4-p-methylphenylpyridine
• CAS NO: 3558-65-4
• Molecular Formula: C24H19N
• Molecular Weight: 321.422
• Mol File: 3558-65-4.mol
• Article Data: 65

Chemical Properties

• CAS DataBase Reference: Pyridine, 4-(4-methylphenyl)-2,6-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 4-(4-methylphenyl)-2,6-diphenyl-(3558-65-4)
• EPA Substance Registry System: Pyridine, 4-(4-methylphenyl)-2,6-diphenyl-(3558-65-4)

Safety Data

• Hazardous Substances Data: 3558-65-4(Hazardous Substances Data)

Upstream product

• 589-18-4 4-Methylbenzyl alcohol 
• 98-86-2 acetophenone 
• 122-00-9 para-methylacetophenone 
• 14428-98-9 N-benzyl-N-(1-phenylethylidene)amine 
• 104-87-0 4-methyl-benzaldehyde 
• 82944-84-1 N-[(1E)-1-phenylethylidene]-P,P-diphenylphosphinic amide 
• 4224-87-7 4-methyl-chalcone 
• 82572-06-3 P,P-diphenyl-N-(1-phenylethylidene)phosphinic amide 
• 536-74-3 phenylacetylene 
• 104-84-7 para-methylbenzylamine 
• 75-05-8 acetonitrile 
• 98-80-6 phenylboronic acid 
• 14939-05-0 1-phenyl-3-(4-methylphenyl)prop-2-yn-1-one 
• 19433-17-1 acetophenone O-acetyloxime 

Downstream Products

• 16263-29-9 C₃₁H₂₃N 
• 499201-95-5 2,6-diphenyl-4-(p-acetoxymethylphenyl)pyridine 
• 499201-96-6 2,6-diphenyl-4-(p-hydroxymethylphenyl)pyridine 
• 97419-28-8 4-(2,6-diphenylpyridin-4-yl)benzaldehyde 
• 161121-63-7 4-(4-(bromomethyl)phenyl)-2,6-diphenylpyridine 

Relevant articles and documents

Heteroatom-Embedded Approach to Vinylene-Linked Covalent Organic Frameworks with Isoelectronic Structures for Photoredox Catalysis

Embedding heteroatoms into the main backbones of polymeric materials has become an efficient tool for tailoring their structures and improving their properties. However, owing to comparatively harsh heteroatom-doping conditions, this has rarely been explo

Synthesis of Kr?hnke pyridines through iron-catalyzed oxidative condensation/double alkynylation/amination cascade strategy

An efficient protocol for the synthesis of symmetrical and unsymmetrical 2,4,6-trisubstituted pyridines via oxidative cascade annulation of arylacetylenes with benzylamines has been developed. The reaction proceeds smoothly utilizing iron(II) triflate as a catalyst and molecular oxygen as an oxidant with broad substrate scope. Mechanistic studies reveal that the reaction may be experiences an oxidative condensation followed by double alkynylation and amination process.

Regiocontrolled synthesis of 2,4,6-triarylpyridines from methyl ketones, electron-deficient acetylenes and ammonium acetate

A novel one-pot two-step approach for the synthesis of 2,4,6-triarylpyridinesvia t-BuOK/DMSO-promotedC-vinylation of a variety of methyl ketones with electron-deficient acetylenes (alkynones) followed by a cyclization of thein situgenerated unsaturated 1,5-dicarbonyl species with ammonium acetate has been developed. This approach possesses competitive advantages such as high regioselectivity, available starting materials and the absence of transition-metal catalysts, oxidants and undesirable byproducts. A wide synthetic utility of the developed approach was demonstrated by the synthesis of trisubstituted, tetrasubstituted and fused pyridines.