300708-60-5

Basic information

• Product Name: 7-METHYL-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE
• Synonyms: 7-METHYL-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE;7-methyl-2-phenyl-3-imidazo[3,2-a]pyridinecarboxaldehyde;7-methyl-2-phenyl-imidazo[3,2-a]pyridine-3-carbaldehyde;7-methyl-2-phenylimidazo[3,2-a]pyridine-3-carbaldehyde
• CAS NO: 300708-60-5
• Molecular Formula: C₁₅H₁₂N₂O
• Molecular Weight: 236.27
• Mol File: 300708-60-5.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-METHYL-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 7-METHYL-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(300708-60-5)
• EPA Substance Registry System: 7-METHYL-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(300708-60-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 300708-60-5(Hazardous Substances Data)

Usage

General Description

7-Methyl-2-phenyl-imidazo[1,2-a]pyridine-3-carbaldehyde is a chemical compound that is categorized under the class of organic compounds known as polycyclic aromatic compounds. These compounds contain at least three fused aromatic rings, in which one or more rings may be non-aromatic. The molecular formula of 7-Methyl-2-phenyl-imidazo[1,2-a]pyridine-3-carbaldehyde is C16H12N2O and it has a molecular weight of 248.28 g/mol. The detailed and specific properties of this chemical, such as its physical and chemical behaviors, its potential uses, and its safety or health implications, are not broadly documented. Further studies might be necessary to update the comprehensive data about this chemical compound.

Upstream product

• 110-18-9 N,N,N,N,-tetramethylethylenediamine 
• 885-91-6 2-phenyl-7-methylimidazo[1,2-a]pyridine 
• 70-11-1 α-bromoacetophenone 
• 68-12-2 N,N-dimethyl-formamide 
• 67-68-5 dimethyl sulfoxide 
• 5350-40-3 N-benzylidene-N-(4-methylpyridin-2-yl)amine 
• 100-52-7 benzaldehyde 
• 1314079-03-2 4-methyl-N-(1-phenylallyl)-2-aminopyridine 
• 695-34-1 2-Amino-4-methylpyridine 

Downstream Products

• 33120-20-6 N-(4-methylpyridin-2-yl)benzamide 

Relevant articles and documents

Aerobic iron(III)-catalyzed direct formylation of imidazo[1,2-a]pyridine using DMSO as carbon source

A novel and efficient iron(III)-catalyzed C3-formylation reaction of imidazo[1,2-a]pyridine in an oxygen atmosphere has been developed. The method is conducted in dimethyl sulfoxide (DMSO), which serves as both the carbonyl carbon source and solvent, in the presence of acetic acid to directly generate structurally diverse 3-formylimidazo[1,2-a]pyridine derivatives in moderate to good yields.

Synthesis, Molecular Docking, BSA, and In Vitro Reactivation Study of Imidazopyridine Oximes Against Paraoxon Inhibited Acetylcholinesterase

Aim: To synthesize and evaluate the fused heterocyclic imidazo[1,2-a]pyridine based oxime as a reactivator against paraoxon inhibited acetylcholinesterase. Background: Organophosphorus compounds (OPs) include parathion, malathion, chlorpyrifos, monocrotop

Copper- A nd DMF-mediated switchable oxidative C-H cyanation and formylation of imidazo[1,2-: A] pyridines using ammonium iodide

The cyanation and formylation of imidazo[1,2-a]pyridines were developed under copper-mediated oxidative conditions using ammonium iodide and DMF as a nontoxic combined cyano-group source and DMF as a formylation reagent. Mechanistic studies indicate that the cyanation of imidazo[1,2-a]pyridines proceeds through a two-step sequence: Initial iodination and then cyanation. The cyanation has a broad substrate scope and high functional group tolerance, and can be safely conducted on a gram scale. A novel copper-mediated formylation using the widely available DMF as the formylation reagent and environmentally friendly molecular oxygen as the oxidant has also been developed. This protocol also provided a convenient approach for the synthesis of clinically used saripidem. This journal is

Visible light induced tetramethylethylenediamine assisted formylation of imidazopyridines

A metal-free visible light induced C-3 formylation of imidazo[1,2-a]pyridine has been developed using tetramethylethylenediamine (TMEDA) as a one carbon source. An array of 3-formyl imidazo[1,2-a]pyridines with wide functionality are synthesized using rose bengal as a photosensitizer under ambient air.