5-Chloro-3-(1-methylpyrrolidin-2-yl)-1H-indole
ADVERTISEMENT
- Molecular formula
- C13H15ClN2
- CAS Number
- 2748327-88-2
- IUPAC Name
- 5-chloro-3-(1-methylpyrrolidin-2-yl)-1H-indole
- Molecular Weight
- 232.72g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3100g/cm3
- Appearance
- and reduce its quality.
- Synonyms
- 5-chloro-3-(1-methylpyrrolidin-2-yl)-1H-indole
Identification
Interesting facts
Exploring 5-Chloro-3-(1-methylpyrrolidin-2-yl)-1H-indole
5-Chloro-3-(1-methylpyrrolidin-2-yl)-1H-indole is a fascinating compound that belongs to the class of indole derivatives, which are known for their diverse biological activities. Here are some interesting facts that highlight its significance:
- Structural Diversity: This compound showcases the unique structural features of indole, a bicyclic structure composed of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
- Pharmacological Potential: Compounds like 5-chloro-3-(1-methylpyrrolidin-2-yl)-1H-indole have been studied for their potential applications in various therapeutic areas, including neuropharmacology and antidepressant activity.
- Synthetic Route: The synthesis of this compound can involve various techniques, including modification of existing indole structures through halogenation and the incorporation of aliphatic amines, illustrating the complexity of organic synthesis.
- Research Insight: As noted in several studies, the introduction of a halogen atom (in this case, chlorine) can enhance the biological activity of indole derivatives, making them potential candidates for drug development.
Overall, the exploration of 5-chloro-3-(1-methylpyrrolidin-2-yl)-1H-indole represents a crucial step in understanding the intricate relationships between chemical structure and biological function. The ongoing research into its properties and applications could uncover new therapeutic avenues in medicinal chemistry.