1019063-41-2

Basic information

• Product Name: 2-amino-4-(4-bromophenyl)-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile
• Synonyms: 2-amino-4-(4-bromophenyl)-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile
• CAS NO: 1019063-41-2
• Molecular Weight: 407.293
• Mol File: 1019063-41-2.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 2-amino-4-(4-bromophenyl)-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4-(4-bromophenyl)-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile(1019063-41-2)
• EPA Substance Registry System: 2-amino-4-(4-bromophenyl)-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile(1019063-41-2)

Safety Data

• Hazardous Substances Data: 1019063-41-2(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 2826-24-6 4-bromobenzylidenemalononitrile 
• 109-77-3 malononitrile 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 1307285-67-1 5-amino-4-(4-bromophenyl)-2-phenylsulfanyl-6,7,8,9-tetrahydrobenzo[b][1,8]-naphthyridine-3-carbonitrile 

Relevant articles and documents

A convenient Baker yeast accelerated, one-pot synthesis of pentasubstituted thiopyridines

Here we report a novel Baker yeast catalyzed one pot cyclocondensation, performed at room temperature in ethanol for obtaining high yields of polyfunctionalized pyridines, 2-amino-4-aryl-3,5-dicyano-6-phenylthiopyridines. The developed protocol obeys cert

First report of multiple metal ions containing glass-ceramic material as a heterogeneous ditopic catalyst for the chromatography free synthesis of 2-amino-3,5-dicarbonitrile-6-arylthio-pyridines in water

This is the first report of the use of multiple metal ions containing glass-ceramic material as a reusable heterogeneous catalyst for multicomponent organic synthesis. A new glass-ceramic material was prepared for this purpose and applied in the sustainab

Borax catalyzed domino reactions: Synthesis of highly functionalised pyridines, dienes, anilines and dihydropyrano[3,2-c]chromenes

Borax, an innocuous, inexpensive, and a naturally occurring material, very efficiently catalyzes the Knoevenagel condensation and Michael addition in domino fashion for the construction of highly functionalised pyridines, dienes, anilines and dihydropyran