96928-03-9

Basic information

• Product Name: 2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-1-(4-chloro-benzyl)-4,6-diphenyl-pyridinium; bromide
• Synonyms: 2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-1-(4-chloro-benzyl)-4,6-diphenyl-pyridinium; bromide
• CAS NO: 96928-03-9
• Molecular Weight: 665.876
• Mol File: 96928-03-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-1-(4-chloro-benzyl)-4,6-diphenyl-pyridinium; bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-1-(4-chloro-benzyl)-4,6-diphenyl-pyridinium; bromide(96928-03-9)
• EPA Substance Registry System: 2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-1-(4-chloro-benzyl)-4,6-diphenyl-pyridinium; bromide(96928-03-9)

Safety Data

• Hazardous Substances Data: 96928-03-9(Hazardous Substances Data)

Upstream product

• 76950-86-2 1-(4-Chloro-benzyl)-4,6-diphenyl-1H-pyridine-2-thione 
• 99-73-0 para-bromophenacyl bromide 
• 96928-02-8 1-(4-Chloro-benzyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-4,6-diphenyl-pyridinium; bromide 

Downstream Products

• 96938-17-9 4,6-diphenyl-2-phenacylthiopyridine 
• 96927-74-1 3-(4-Chloro-phenyl)-2,5,7-triphenyl-indolizine 
• 96927-64-9 2-[1-(4-Chloro-benzyl)-4,6-diphenyl-1H-pyridin-(2E)-ylidene]-1-phenyl-ethanone 
• 96927-75-2 2-(4-Bromo-phenyl)-3-(4-chloro-phenyl)-5,7-diphenyl-indolizine 
• 96928-02-8 1-(4-Chloro-benzyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-4,6-diphenyl-pyridinium; bromide 
• 622-95-7 4-chlorobenzyl bromide 
• 96927-65-0 1-(4-Bromo-phenyl)-2-[1-(4-chloro-benzyl)-4,6-diphenyl-1H-pyridin-(2E)-ylidene]-ethanone 
• 27047-19-4 1-(4-bromophenyl)-2-phenylsulfanylethanone 
• 76950-86-2 1-(4-Chloro-benzyl)-4,6-diphenyl-1H-pyridine-2-thione 

Relevant articles and documents

Synthesis Using Pyridinium Anhydrobases. Preparation of Indolizine Derivatives

A number of derivatives of indolizine ring system have been prepared from 1-substituted 4,6-diphenyl-2-phenacylidene-1,2-dihydropyridines either by metallation with LDA or acylation and further basic treatment.Similarly, 1-arylmethyl-4,6-diphenyl-2-dicyanomethylene-1,2-dihydropyridines by action of LDA undergo cyclization to the corresponding 2-amino-1-cyano-3-aryl indolizinies.