82193-32-6

Basic information

• Product Name: Imidazo[1,2-a]pyridine-2-carbonitrile, 3-amino-
• Synonyms: Imidazo[1,2-a]pyridine-2-carbonitrile, 3-amino-
• CAS NO: 82193-32-6
• Molecular Formula: C8H6N4
• Molecular Weight: 0
• Mol File: 82193-32-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Imidazo[1,2-a]pyridine-2-carbonitrile, 3-amino-(CAS DataBase Reference)
• NIST Chemistry Reference: Imidazo[1,2-a]pyridine-2-carbonitrile, 3-amino-(82193-32-6)
• EPA Substance Registry System: Imidazo[1,2-a]pyridine-2-carbonitrile, 3-amino-(82193-32-6)

Safety Data

• Hazardous Substances Data: 82193-32-6(Hazardous Substances Data)

Upstream product

• 62195-05-5 2-cyano-3-nitroimidazoimidazo[1,2-a]pyridine 
• 79917-37-6 2-nitrosopyridine 
• 109-77-3 malononitrile 
• 504-29-0 2-aminopyridine 
• 3999-05-1 2-chloroimidazo[1,2-a]pyridine 
• 126202-06-0 2-(2-imino-1,2-dihydropyridin-1-yl)acetic acid 
• 4926-52-7 2-chloro-3-nitroimidazo[1,2-a]pyridine 
• 62195-32-8 3-nitroimidazo[1,2-a]pyridine-2-carboxamide 

Relevant articles and documents

Some nucleophilic substitutions in 2-cyano-3-nitroimidazo[1,2-a]pyridine

In some nucleophilic substitution reactions of 2-cyano-3-nitroimidazo[1,2- a]pyridine, nitrogen (alkylamines, guanidine) and oxygen nucleophiles (alkoxides) underwent substitution of the 2-cyano group, while sulfur nucleophiles (alkylthiols) underwent sub

Synthesis of enaminonitrile imidazo[1. 2-a]pyridine by an Ehrlich-Sachs type reaction on 2-nitrosopyridine

An Erlich-Sachs type reaction on 2-nitrosopyridines with malononitrile and a few drops of triethylamine produced 3-amino-2-cyanoimidazo[1,2-a]pyridines directly. The structure of the enaminonitrile was confirmed by an independent synthesis and chemical behavior. The imidazopyridine nitroester derivative used in the synthesis was employed as a synthon in an alternative route to pyridoimidazopyrimidones.