28036-31-9

Basic information

• Product Name: 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE
• Synonyms: 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE;3-Amino-2-methylimidazo[1,2-a]pyridine
• CAS NO: 28036-31-9
• Molecular Formula: C₈H₉N₃
• Molecular Weight: 147.18
• Product Categories: Heterocycles series;Amines;Fused Ring Systems
• Mol File: 28036-31-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Density: 1.27±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 9.08±0.10(Predicted)
• CAS DataBase Reference: 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE(28036-31-9)
• EPA Substance Registry System: 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE(28036-31-9)

Safety Data

• Hazardous Substances Data: 28036-31-9(Hazardous Substances Data)

Usage

General Description

2-Methylimidazo[1,2-a]pyridin-3-amine is a chemical compound with the molecular formula C8H8N4. It is a heterocyclic organic compound that can be found in various pharmaceutical drugs. The compound has a fused-ring structure containing both imidazole and pyridine rings, which gives it unique chemical and biological properties. 2-Methylimidazo[1,2-a]pyridin-3-amine has been studied for its potential use in the treatment of various diseases, including cancer and neurological disorders. Its specific biochemical interactions and mechanisms of action are still being investigated, making it an active area of research in medicinal chemistry and drug development.

Upstream product

• 504-29-0 2-aminopyridine 
• 151-50-8 potassium cyanide 
• 918-04-7 potassium 1-hydroxyethane-1-sulfonate 
• 34165-09-8 2-methyl-3-nitroimidazo[1,2-a]pyridine 
• 934-37-2 2-methylimidazo[1,2-a]pyridine 

Downstream Products

• 406207-66-7 N-(2-methyl-imidazo[1,2-a]pyridin-3-yl)-benzamide 

Relevant articles and documents

3-Benzamido, ureido and thioureidoimidazo[1,2-a]pyridine derivatives as potential antiviral agents

This work reports the synthesis and the antiviral activities of 3-benzamido, 3-phenylureido and 3-phenylthioureido derivatives in the imidazo[1,2-a]pyridine series. The structure was proven by NMR spectroscopy. The synthesized compounds were evaluated against a large number of viruses. The 3-phenylthioureido derivative 7 showed moderate activity against human cytomegalovirus (HCMV) in vitro. The crystallographic data for 8 are also reported and explain the absence of activity against human immunodeficiency virus (HIV).

Studies on Heterocyclic Compounds: Part I. Synthesis of 3-amino-2-sub-Imidazo(1,2-a)-pyridines

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