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