817172-44-4

Basic information

• Product Name: 2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE
• Synonyms: 2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE;2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE
• CAS NO: 817172-44-4
• Molecular Formula: C₁₄H₉N₃O₃
• Molecular Weight: 267.24
• Mol File: 817172-44-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(817172-44-4)
• EPA Substance Registry System: 2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE(817172-44-4)

Safety Data

• Hazardous Substances Data: 817172-44-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE is used as a key intermediate in the synthesis of various organic compounds. Its presence of the aldehyde functional group allows for a wide range of chemical reactions, making it a versatile building block in the creation of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE is used as a starting material for the development of new pharmaceutical agents. Its structural features, including the nitro-phenyl and imidazo[1,2-a]pyridine rings, may contribute to the compound's biological activity, making it a promising candidate for drug discovery.
Used in Drug Discovery and Development:
2-(4-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE is used as a potential lead compound in drug discovery and development. Its unique structural elements and biological activities suggest that it may have therapeutic potential, warranting further research and exploration in the development of new medications.

Upstream product

• 504-29-0 2-aminopyridine 
• 100-19-6 (4-nitrophenyl)ethanone 
• 3323-26-0 2-(4-nitrophenyl)imidazo[1,2-a]pyridine 
• 68-12-2 N,N-dimethyl-formamide 
• 99-81-0 4-Nitrophenacyl bromide 

Downstream Products

• 1417910-22-5 C₁₄H₁₀N₆O₂ 
• 1417910-31-6 3-((4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)methyl)-2-(3-nitrophenyl)-1H-imidazo[1,2-a]pyridine 

Relevant articles and documents

One-pot multicomponent synthesis of novel substituted imidazo[1,2-a]pyridine incorporated thiazolyl coumarins and their antimicrobial activity

A series of novel substituted imidazo[1,2-a]pyridine incorporated thiazolyl coumarin derivatives (4a, 4b, 4c, 4d, 4e, 4f, 4g, 4h, 4i, 4j, 4k, 4l, 4m, 4n, 4o, 4p, 4q, 4r, 4s, 4t) were synthesized in good yields via one-pot multicomponent condensation of su

Exploration of the CuAAC reaction for the synthesis of novel 3-(triazol-1-yl)methyl-imidazo[1,2-a]pyridines

The archetypical CuAAC click chemistry is explored to assemble diverse 3-(triazol-1-yl)methyl-imidazo[1,2-a]pyridines. The approach is simple, general, and environmentally benign to generate a library of novel triazolo-imidazo[1,2- a]pyridine derivatives in good yield (30-90%).