75007-92-0

Basic information

• Product Name: 3H-Imidazo[4,5-c]pyridine, 2-phenyl-
• Synonyms: 3H-Imidazo[4,5-c]pyridine, 2-phenyl-;2-Phenylimidazo[4,5-c]pyridine
• CAS NO: 75007-92-0
• Molecular Formula: C₁₂H₉N₃
• Molecular Weight: 195
• Mol File: 75007-92-0.mol
• Article Data: 13

Chemical Properties

• Melting Point: 229-230℃
• Boiling Point: 428.5°Cat760mmHg
• Flash Point: 206.8°C
• Appearance: /
• Density: 1.270
• Vapor Pressure: 1.51E-07mmHg at 25°C
• Refractive Index: 1.699
• PKA: 9.45±0.30(Predicted)
• CAS DataBase Reference: 3H-Imidazo[4,5-c]pyridine, 2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Imidazo[4,5-c]pyridine, 2-phenyl-(75007-92-0)
• EPA Substance Registry System: 3H-Imidazo[4,5-c]pyridine, 2-phenyl-(75007-92-0)

Safety Data

• Hazardous Substances Data: 75007-92-0(Hazardous Substances Data)

Usage

General Description

3H-Imidazo[4,5-c]pyridine, 2-phenyl- is a chemical compound with a unique structure containing a fused imidazole and pyridine ring system. It is a heterocyclic compound that is often used as a building block in organic synthesis. 3H-Imidazo[4,5-c]pyridine, 2-phenyl- has potential applications in pharmaceuticals, agrochemicals, and materials science due to its diverse and versatile reactivity. Additionally, its unique structure and properties make it a valuable tool for the development of new compounds with interesting and useful properties. Due to its potential for a wide range of applications, research and development efforts continue to explore the uses of 3H-Imidazo[4,5-c]pyridine, 2-phenyl- in various fields.

InChI:InChI=1/C12H9N3/c1-2-4-9(5-3-1)12-14-10-6-7-13-8-11(10)15-12/h1-8H,(H,14,15)

Upstream product

• 54-96-6 3,4-diaminopyridine 
• 100-52-7 benzaldehyde 
• 2876-13-3 N-benzylpyridinium chloride 
• 65-85-0 benzoic acid 
• 80862-35-7 1-Benzyl-3-amino-1,4-dihydro-4-pyridoneimine 
• 75115-28-5 N⁽³⁾-benzylpyridine-3,4-diamine 
• 80862-36-8 1-Benzyl-3,4-diaminopyridinium chloride 
• 918550-20-6 N-(3-aminopyridin-4-yl)benzamide 
• 504-24-5 4-aminopyridine 
• 5221-44-3 N-(pyridin-4-yl)benzamide 
• 93-97-0 benzoic acid anhydride 
• 1025874-45-6 N-(3-nitropyridin-4-yl)benzamide 
• 1678-49-5 3-Bromo-4-nitropyridine N-oxide 
• 91397-37-4 4-nitro-3-benzylaminopyridine 1-oxide 

Downstream Products

• 98383-05-2 C₂₆H₂₂N₈O₅S₂ 
• 1219458-23-7 3-benzyl-2-phenylimidazo[4,5-c]pyridine 

Relevant articles and documents

Substituted 5-benzyl-2-phenyl-5H-imidazo[4,5-c]pyridines: A new class of pestivirus inhibitors

A novel class of inhibitors of pestiviruses (5-substituted 2-phenyl-5H-imidazo[4,5-c]pyridines) is described. Modification of the substituent in position 5 resulted in analogues with high activity (EC50 1000) aga

A one-step synthesis of substituted benzo- and pyridine-fused 1H-imidazoles

Substituted benzimidazoles and pyrimidazoles are an important group of heterocyclic aromatic organic compounds in the field of medicinal chemistry. A one-step microwave accelerated synthesis of substituted benzo- and pyridine-fused 1H-imidazoles has been described. Mechanistically, the reaction proceeds by reacting substituted 2-fluoronitrobenzene and substituted arylamine through the formation of N-hydroxy intermediate, which at higher temperature cleaves to afford the desired product. This approach achieved reductions in reaction times, higher yields, cleaner reactions than the previously described synthetic processes.

Photophysics of 2-(4′-amino-2′-hydroxyphenyl)-1H-imidazo-[4,5- c ]pyridine and its analogues: Intramolecular proton transfer versus intramolecular charge transfer

Photophysical characteristics of 2-(4′-amino-2′-hydroxyphenyl)-1H-imidazo-[4,5-c]pyridine (AHPIP-c) have been studied in various aprotic and protic solvents using UV-visible, steady state fluorescence and time-resolved fluorescence spectroscopic technique

Selective autoxidation of benzylamines: Application to the synthesis of some nitrogen heterocycles

A green and remarkably simple synthesis of nitrogen heterocycles from benzylamines and anilines o-substituted by a cyclizable group has been developed based on selective uncatalyzed autoxidation of benzylamines.