55843-91-9

Basic information

• Product Name: 4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE
• Synonyms: 4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE;4-Imidazo[1,2-a]pyridin-2-yl-benzonitrile >97%
• CAS NO: 55843-91-9
• Molecular Formula: C₁₄H₉N₃
• Molecular Weight: 219.24
• Mol File: 55843-91-9.mol
• Article Data: 34

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE(55843-91-9)
• EPA Substance Registry System: 4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE(55843-91-9)

Safety Data

• Hazardous Substances Data: 55843-91-9(Hazardous Substances Data)

Usage

Description

4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE is a heterocyclic organic compound with the molecular formula C16H10N4. It features a benzene ring fused to an imidazole and pyridine ring, making it a valuable building block in medicinal chemistry for the synthesis of pharmaceutical drugs and agrochemicals.

Uses

Used in Pharmaceutical Industry:
4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE is used as a key intermediate for the synthesis of various pharmaceutical drugs due to its unique structure and properties, which contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE also serves as a building block for the synthesis of agrochemicals, playing a crucial role in the development of new agrochemical products with enhanced efficacy and selectivity.
Used in Research and Development:
4-IMIDAZO[1,2-A]PYRIDIN-2-YL-BENZONITRILE is utilized in research and development laboratories to explore its potential pharmacological activities and biological properties, further expanding its applications in the field of medicinal and pharmaceutical chemistry.

Upstream product

• 504-29-0 2-aminopyridine 
• 1443-80-7 4-cyanophenyl methyl ketone 
• 20099-89-2 4-Cyanophenacyl bromide 
• 70-11-1 α-bromoacetophenone 
• 25309-65-3 4-ethylbenzonitrile 
• 623-00-7 4-bromobenzenecarbonitrile 
• 99-73-0 para-bromophenacyl bromide 
• 34658-66-7 2-(4-bromophenyl)imidazo[1,2-a]pyridine 
• 75-52-5 nitromethane 
• 105-07-7 4-cyanobenzaldehyde 
• 110-86-1 pyridine 
• 717126-40-4 C₁₁H₉N₅ 
• 131356-52-0 2,2-dibromo-1-(4-cyanophenyl)ethene 
• 31827-94-8 2-bromo-1-(4-iodophenyl)ethanone 

Downstream Products

• 1118020-89-5 4-(3-phenylimidazo[1,2-a]pyridin-2-yl)benzaldehyde 
• 118000-50-3 4-Imidazo[1,2-a]pyridin-2-yl-benzamidine; hydrochloride 
• 118001-89-1 (E)-3-(4-Imidazo[1,2-a]pyridin-2-yl-phenyl)-acrylic acid ethyl ester 
• 118001-62-0 4-(3-Nitro-imidazo[1,2-a]pyridin-2-yl)-benzaldehyde 
• 118001-90-4 (E)-3-(4-Imidazo[1,2-a]pyridin-2-yl-phenyl)-prop-2-en-1-ol 
• 118001-64-2 4-(5,6,7,8-Tetrahydro-imidazo[1,2-a]pyridin-2-yl)-benzaldehyde 
• 118001-61-9 4-(3-bromoimidazo[1,2-a]pyridin-2-yl)benzaldehyde 
• 118001-87-9 2-<4'-(3-oxo-1-propenyl)phenyl>imidazo<1,2-a>pyridine 
• 118036-05-8 4-Imidazo[1,2-a]pyridin-2-yl-thiobenzamide 
• 118000-49-0 2-(4-Aminocarbonyl-phenyl)-imidazo[1,2-a]pyridine 

Relevant articles and documents

Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach

Herein, we describe the bromomethyl acyl boronate linchpin-an enabling reagent for the condensation-driven assembly of novel bis(heteroaryl) motifs. This building block is readily accessible from commercially available starting materials. A variety of 2-a

Iodine-Mediated Sulfenylation of Imidazo[1,2- a ]pyridines with Ethyl Arylsulfinates

A simple iodine-mediated approach is reported for the synthesis of sulfenylated imidazo[1,2- a ]pyridines through the reaction of imidazo[1,2- a ]pyridines with ethyl arylsulfinates under mild conditions. The reaction scope was investigated, and a plausible mechanism is proposed to elucidate the reaction process and activation mode. The results indicate that ethyl sulfinates are efficient sulfur sources for the construction of C-S bonds.

Solvent and catalyst-free synthesis of imidazo[1,2-a]pyridines by grindstone chemistry

The present work describes the solvent and catalyst-free synthesis of imidazo[1,2-a]pyridines in excellent to nearly quantitative yields from 2-aminopyridines and a wide variety of ω-bromomethylketones using a grindstone procedure at 25°C to 30°C for 3 to