5-Chloro-3-phenyl-2-[4-(pyrrolidin-1-ylethoxy)phenyl]-1H-indole
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- Molecular formula
- C28H27ClN2O
- CAS Number
- 91573-81-2
- IUPAC Name
- 5-chloro-3-phenyl-2-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-1H-indole
- Molecular Weight
- 426.99g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3000g/cm3
- Synonyms
- INDOLE, 5-CHLORO-3-PHENYL-2-(p-(2-(1-PYRROLIDINYL)ETHOXY)PHENYL)-
Identification
Interesting facts
Interesting Facts about 5-Chloro-3-phenyl-2-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-1H-indole
This compound is a fascinating member of the indole family, showcasing a unique structure that contributes to its intriguing properties and potential applications. Here are some compelling aspects to consider:
- Pharmacological Potential: Compounds like this one often play a crucial role in medicinal chemistry. Indoles are known for their diverse biological activities, which might include anti-cancer or anti-inflammatory effects, making them valuable in drug design.
- Complex Structure: The incorporation of a chloro group and a pyrrolidine moiety adds layers of complexity, which can enhance the compound's ability to interact with biological targets through various mechanisms.
- Research Significance: The study of indole derivatives is vibrant in scientific literature, as they can lead to novel therapeutic agents. This compound’s specific structure may provide insights or pathways for further development in pharmaceuticals.
- Versatile Synthesis: Compounds containing indole rings can often be synthesized using a variety of methods, including cyclization reactions and substitution techniques, contributing to their accessibility in the lab.
- Structure-Activity Relationship (SAR): Scientists often explore how changes in the compound's structure affect its biological activity. Understanding these relationships can be pivotal for optimizing therapeutic efficacy.
In summary, 5-chloro-3-phenyl-2-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-1H-indole stands at a crossroads of chemistry and biology. Its unique composition invites further investigation into its potential utility in pharmacology as well as its fundamental chemical behavior.