3-(1-Methylpyrrolidin-3-yl)-1H-indole

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Identification

Molecular formula
C13H16N2
CAS Number
1048973-47-2
IUPAC Name
3-(1-methylpyrrolidin-3-yl)-1H-indole
Molecular Weight
198.28g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1500g/cm3
Synonyms
3671-00-9
Interesting facts

Interesting Facts about 3-(1-Methylpyrrolidin-3-yl)-1H-Indole

3-(1-Methylpyrrolidin-3-yl)-1H-indole represents a fascinating class of compounds known for their diverse applications in medicinal chemistry and pharmacology. Below are some engaging insights regarding this intriguing compound:

  • Structural Innovation: The presence of the indole moiety, combined with a pyrrolidine ring, provides a unique structural foundation that can influence biological activity significantly.
  • Biological Relevance: Indole derivatives are often found in nature and can act as crucial intermediates in the synthesis of various pharmaceuticals. The pyrrolidine part adds to its potential for creating novel therapeutic agents.
  • Potential Activity: Compounds containing indole structures are widely studied due to their potential roles as anticancer agents, antidepressants, and anti-inflammatory drugs. Their ability to interact with various biological targets makes them compelling subjects of research.
  • Research and Development: Many studies have shown that modifications to the indole backbone can lead to significant enhancements in efficacy and selectivity, thus making compounds like 3-(1-methylpyrrolidin-3-yl)-1H-indole crucial in drug design.
  • Pharmacophore Modeling: The study of the pharmacophore—features of the molecule necessary to ensure interaction with biological macromolecules—gains from the distinct arrangement of atoms in this compound, aiding in predicting interactions.
  • Versatile Synthesis: Researchers have developed various synthetic pathways to obtain compounds like this indole derivative, showcasing the versatility of organic synthesis techniques.

As a vivid example of the intersection between chemistry and biological sciences, 3-(1-methylpyrrolidin-3-yl)-1H-indole continues to be a promising area of research, ripe with possibilities for new discoveries and applications in drug development. Its unique structural characteristics facilitate a wide range of investigations into novel therapeutic avenues.

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