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- Molecular formula
- C13H12N2
- CAS Number
- 244-61-1
- IUPAC Name
- 3-[2-(4-pyridyl)ethyl]-1H-indole
- Molecular Weight
- 182.23g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2300g/cm3
- Appearance
- may become slightly off-color upon exposure to air or light over time. It is typically obtained in its crystalline form.
- Synonyms
- INHIBITOR OF P38 KINASE
Identification
Interesting facts
Interesting Facts about 3-[2-(4-pyridyl)ethyl]-1H-indole
3-[2-(4-pyridyl)ethyl]-1H-indole is a fascinating compound that plays a significant role in various scientific fields, especially in medicinal chemistry and research applications. Here are some compelling aspects to consider:
- Structural Diversity: The compound features an indole core, which is a bicyclic structure that comprises a fused benzene and pyrrole ring. This structural diversity contributes to its numerous biological activities.
- Biological Significance: Indole derivatives, including this compound, are known for their potential therapeutic properties, including anti-cancer and anti-inflammatory effects. They often interact with biological targets in significant ways.
- Pyridine Integration: The presence of the 4-pyridyl group enhances its chemical properties, making it a valuable target for various chemical transformations or interactions.
- Research Applications: Due to its unique structure, it is of interest in the study of receptor binding and cellular signaling pathways, which have implications in pharmacology and drug design.
- Versatile Chemical Reactions: This compound can be subjected to a variety of chemical reactions, including nucleophilic substitutions and coupling reactions, which are fundamental in the synthesis of more complex molecules.
As a chemical scientist, exploring 3-[2-(4-pyridyl)ethyl]-1H-indole opens up pathways to not only develop new pharmaceuticals but also to enhance our understanding of biochemical processes. The compound’s versatility and potential for innovation make it an exciting subject of study in contemporary chemistry.