Nicotine tert-indole
- Molecular formula
- C16H20N2
- CAS Number
- 1535490-20-4
- IUPAC Name
- 3-(1,5-dimethylpyrrolidin-2-yl)-1H-indole
- Molecular Weight
- 240.34g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2000g/cm3
- Synonyms
- 3-(1, 5-dimethylpyrrolidin-2-yl)-1H-indole
Identification
Interesting Facts about 3-(1,5-Dimethylpyrrolidin-2-yl)-1H-Indole
3-(1,5-Dimethylpyrrolidin-2-yl)-1H-indole is a fascinating compound that draws attention for its unique structure and potential applications. As a derivative of indole, a fundamental building block in organic chemistry, this compound exhibits intriguing characteristics and pharmacological properties.
1. Structural Significance
The presence of the 1,5-dimethylpyrrolidin moiety adds a layer of complexity to the indole structure, enabling diverse interactions with biological targets. Specifically, its structure can influence:
- Receptor binding: The unique arrangement may enhance its ability to interact with various receptors in the body.
- Chemical reactivity: Alterations in its electronic distribution can affect its reactivity and stability under different conditions.
2. Biological Potential
This compound is notable for its potential therapeutic applications. Research has indicated that indole derivatives can possess:
- Antidepressant effects: Some studies suggest that compounds similar to 3-(1,5-dimethylpyrrolidin-2-yl)-1H-indole may exhibit mood-enhancing properties.
- Anticancer activity: Indole derivatives are known for their ability to interfere with cancer cell proliferation.
- Antimicrobial properties: There is growing interest in the antimicrobial effects of indole-based compounds, making this a subject of intense study.
3. Applications in Synthesis
Beyond its biological significance, 3-(1,5-dimethylpyrrolidin-2-yl)-1H-indole serves as an important precursor in organic synthesis, utilized in creating other complex molecules. It can be used in:
- Pharmaceutical research: As a scaffold for drug design, facilitating the development of new therapeutics.
- Material science: In the synthesis of polymers and novel materials due to its unique chemical properties.
In summary, 3-(1,5-dimethylpyrrolidin-2-yl)-1H-indole exemplifies how **structural innovation** in chemical compounds can lead to significant advancements in both scientific research and real-world applications. Its potential as a multi-functional compound enhances its value in both academic and industrial settings.