96928-02-8

Basic information

• Product Name: 1-(4-Chloro-benzyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-4,6-diphenyl-pyridinium; bromide
• Synonyms: 1-(4-Chloro-benzyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-4,6-diphenyl-pyridinium; bromide
• CAS NO: 96928-02-8
• Molecular Weight: 586.98
• Mol File: 96928-02-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-Chloro-benzyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-4,6-diphenyl-pyridinium; bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Chloro-benzyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-4,6-diphenyl-pyridinium; bromide(96928-02-8)
• EPA Substance Registry System: 1-(4-Chloro-benzyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-4,6-diphenyl-pyridinium; bromide(96928-02-8)

Safety Data

• Hazardous Substances Data: 96928-02-8(Hazardous Substances Data)

Upstream product

• 76950-86-2 1-(4-Chloro-benzyl)-4,6-diphenyl-1H-pyridine-2-thione 
• 96928-03-9 2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-1-(4-chloro-benzyl)-4,6-diphenyl-pyridinium; bromide 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 622-95-7 4-chlorobenzyl bromide 
• 96928-03-9 2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-1-(4-chloro-benzyl)-4,6-diphenyl-pyridinium; bromide 
• 96927-65-0 1-(4-Bromo-phenyl)-2-[1-(4-chloro-benzyl)-4,6-diphenyl-1H-pyridin-(2E)-ylidene]-ethanone 
• 96927-75-2 2-(4-Bromo-phenyl)-3-(4-chloro-phenyl)-5,7-diphenyl-indolizine 
• 96927-74-1 3-(4-Chloro-phenyl)-2,5,7-triphenyl-indolizine 
• 96938-17-9 4,6-diphenyl-2-phenacylthiopyridine 
• 96927-64-9 2-[1-(4-Chloro-benzyl)-4,6-diphenyl-1H-pyridin-(2E)-ylidene]-1-phenyl-ethanone 
• 16222-10-9 1-phenyl-2-(phenylthio)ethanone 
• 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.