5-bromo-3-(4,5,6,7-tetrahydro-1H-indol-2-ylmethylene)indolin-2-one

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Identification

Molecular formula
C16H13BrN2O
CAS Number
4378-41-0
IUPAC Name
5-bromo-3-(4,5,6,7-tetrahydro-1H-indol-2-ylmethylene)indolin-2-one
Molecular Weight
309.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4342g/cm3
Synonyms
5-Bromo-1, 3-dihydro-3-[(4, 5, 6, 7-tetrahydro-1H-indol-2-yl)methylene]-2H-indol-2-one
Interesting facts

Interesting Facts about 5-Bromo-3-(4,5,6,7-tetrahydro-1H-indol-2-ylmethylene)indolin-2-one

5-Bromo-3-(4,5,6,7-tetrahydro-1H-indol-2-ylmethylene)indolin-2-one is a fascinating compound known for its diverse potential applications in medicinal chemistry and organic synthesis. Here are some intriguing aspects of this compound:

  • Diverse Structures: This compound contains both indolin and indole structures, which are commonly found in a variety of natural products and pharmaceuticals.
  • Potential Biological Activity: The structural characteristics of this compound suggest potential activity against various biological targets, making it a subject of interest for drug discovery.
  • Halogenation Influence: The presence of the bromine atom not only adds to the compound's reactivity but may also influence its interaction with biological systems, which is crucial in medicinal chemistry.
  • Synthetic Utility: Its synthesis can involve various modern organic reactions, showcasing the versatility and creativity in synthetic organic chemistry practices.

The study of compounds like 5-bromo-3-(4,5,6,7-tetrahydro-1H-indol-2-ylmethylene)indolin-2-one expands our understanding of chemical behavior and opens new doors in the quest for effective pharmaceuticals. As one chemical researcher aptly noted, "Every compound tells a story of its reactivity and potential utility." Through deeper exploration, we can uncover those narratives and harness the power of such compounds in meaningful ways.

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