1284293-40-8

Basic information

• Product Name: (6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone
• Synonyms: (6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone
• CAS NO: 1284293-40-8
• Molecular Formula: C₁₄H₉BrN₂O
• Molecular Weight: 301.13806
• Mol File: 1284293-40-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 144-146℃ (ethanol )
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone(1284293-40-8)
• EPA Substance Registry System: (6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone(1284293-40-8)

Safety Data

• Hazardous Substances Data: 1284293-40-8(Hazardous Substances Data)

Usage

General Description

(6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone is a chemical compound with the molecular formula C14H9BrN2O. It is a heterocyclic organic compound that contains an imidazo[1,2-a]pyridine ring system and a phenylmethanone functional group. (6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone is a valuable building block for the synthesis of pharmaceuticals and agrochemicals, and it is also used as a reagent in organic synthesis. It has potential applications in medicinal chemistry due to its ability to modulate biological targets, and it is also of interest in the field of material science for the development of novel organic materials. The synthesis and characterization of (6-Bromoimidazo[1,2-a]pyridin-3-yl)phenylmethanone are of interest to researchers in various scientific disciplines for its potential use in a wide range of applications.

Upstream product

• 22259-90-1 3-((5-bromopyridin-2-yl)amino)-1-phenylpropan-1-one 
• 1072-97-5 5-bromo-2-pyridylamine 
• 138240-34-3 (E)-N’-(5-bromopyridin-2-yl)-N,N-dimethylformamidine 
• 70-11-1 α-bromoacetophenone 
• 2579-22-8 Phenylpropargyl aldehyde 

Downstream Products

• 328062-45-9 6-phenylimidazo[1,2-a]pyridine 

Relevant articles and documents

Transition metal-mediated C=O and C=C bond-forming reactions: A regioselective strategy for the synthesis of imidazo[1,2- A ]pyridines and imidazo[1,2- A ]pyrazines

A novel and convenient transformation for the regiospecific synthesis of functionalized imidazo[1,2-a]pyridine aldehydes/ketones and 3-vinyl imidazo[1,2-a]pyridines has been developed via copper(I)- and palladium(II)-catalyzed cyclization. The one-pot reaction proceeds smoothly with commercially available catalysts and affords the products in moderate to good yields. It represents an efficient approach for the formation of C-N, C=O, and C=C bonds under mild conditions.

I2-catalyzed intramolecular oxidative amination of C(sp3)-H bond: Efficient access to 3-acylimidazo[1,2-: A] pyridines under neat condition

An efficient and "green" protocol for the synthesis of 3-acylimidazo[1,2-a]pyridines through intramolecular oxidative α-amination of carbonyl compounds has been developed. The reaction proceeds smoothly utilizing I2 as a catalyst and H2O2 as an oxidant under neat condition with broad substrate scope. Several complex nitrogen-containing fused rings are conveniently constructed, which are not easy to access by traditional methods.

Convenient two-step one-pot synthesis of 3-substituted imidazo[1,2-a]pyridines and imidazo[1,2-b]pyridazines

Abstract: A convenient and novel two-step one-pot method for the synthesis of 3-substituted imidazo[1,2-a]pyridines and 3-substituted imidazo[1,2-b]pyridazines was developed through the reaction of heterocyclic amines and N,?N-dimethylformamide dimethyl a