86018-76-0

Basic information

• Product Name: 4-(2'-chlorophenyl)-2,6-diphenylpyridine
• Synonyms: 4-(2'-chlorophenyl)-2,6-diphenylpyridine
• CAS NO: 86018-76-0
• Molecular Weight: 341.84
• Mol File: 86018-76-0.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: 4-(2'-chlorophenyl)-2,6-diphenylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2'-chlorophenyl)-2,6-diphenylpyridine(86018-76-0)
• EPA Substance Registry System: 4-(2'-chlorophenyl)-2,6-diphenylpyridine(86018-76-0)

Safety Data

• Hazardous Substances Data: 86018-76-0(Hazardous Substances Data)

Upstream product

• 79-46-9 2-nitropropane 
• 89-98-5 2-chloro-benzaldehyde 
• 82944-84-1 N-[(1E)-1-phenylethylidene]-P,P-diphenylphosphinic amide 
• 98-86-2 acetophenone 
• 3300-67-2 3-(2-chlorophenyl)-1-phenylpropenone 
• 613-91-2 acetophenone oxime 
• 19433-17-1 acetophenone O-acetyloxime 
• 95-49-8 2-methylchlorobenzene 
• 2444-36-2 2'-chloro-benzeneacetic acid 
• 75-05-8 acetonitrile 
• 98-80-6 phenylboronic acid 
• 86169-24-6 2-amino-(2-chlorophenyl)ethanoic acid 
• 89-97-4 2-CHLOROBENZYLAMINE 
• 22966-11-6 (2E)-3-(2-chlorophenyl)-1-phenylprop-2-en-1-one 

Relevant articles and documents

Pyridine Skeleton Synthesis Using Acetonitrile as C4N1 Units and Solvent

The first [3 + 2 + 1] methodology for pyridine skeleton synthesis via cascade carbopalladation/cyclization of acetonitrile, arylboronic acids, and aldehydes was developed. This reaction proceeds via six step tandem reaction sequences involving the carbopalladation reaction of acetonitrile, a nucleophilic addition, a condensation, an intramolecular Michael addition, cyclization, and aromatization. Delightfully, both palladium acetate and supported palladium nanoparticles catalyzed this reaction with similar catalytic performance. The characterization results of the fresh and used supported palladium nanoparticle catalysts indicated that the reaction might be performed via a Pd(0)/Pd(II) catalytic cycle that began with Pd(0). Furthermore, the products showed good fluorescence characteristics. The green homogeneous/heterogenous catalytic methodologies pave a new way for constructing the pyridine skeleton.

Method for synthesizing pyridine ring structure by utilizing cascade reaction of aldehyde, arylboronic acid and acetonitrile

The invention discloses a method for synthesizing a pyridine ring structure by utilizing cascade reaction of aldehyde, arylboronic acid and acetonitrile, which comprises the following steps: dissolving a palladium catalyst, aldehyde, arylboronic acid, a l

An efficient, green solvent-free protocol for the synthesis of 2,4,6-triarylpyridines using reusable heterogeneous activated Fuller’s earth catalyst

Abstract: A simple, efficient, and green method of preparation for the synthesis of highly substituted pyridines by multicomponent reaction of acetophenones, aldehydes, and ammonium acetate using activated Fuller’s earth as an effective and reusable heterogeneous catalyst is described. The advantages of the present protocol include simple procedure with an easy workup procedure, mild reaction conditions, and high yields of the products. The performance of this reaction under solvent-free conditions using heterogeneous catalysts, such as activated Fuller’s earth, could enhance its efficiency from an economic as well as ecological point of view. Graphical abstract: [Figure not available: see fulltext.].