Indole-3,3'-pyrrole-2,5-dione
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- Molecular formula
- C18H11N3O2
- CAS Number
- 24424-99-5
- IUPAC Name
- 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione
- Molecular Weight
- 297.31g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4600g/cm3
- Appearance
- 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione is commonly seen as an orange-red or reddish powder. The compound tends to form crystalline structures showing clear definition and geometric edges when examined closely. It can be varied from dull to more glistening surfaces depending on purity and particle size.
- Synonyms
- bisindolylmaleimide iv
Identification
Interesting facts
Interesting Facts about 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione
3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione, commonly referred to as a bis-indole derivative, showcases some fascinating characteristics deserving of deeper exploration:
- Biological Relevance: This compound belongs to a class of molecules known for their biological activity. Indole-based compounds are often found in nature and have been associated with various medicinal properties, including antimicrobial and anticancer activities.
- Chemical Structure: The unique structure features two indole moieties linked to a pyrrole-2,5-dione core. This configuration is important for its electronic properties, which can influence the reactivity and interactions of the compound.
- Potential Applications: Researchers are examining similar compounds for applications in pharmaceuticals and organic electronics, highlighting the diverse potential of indole derivatives in modern science.
- Synthetic Pathways: The synthesis of this compound typically involves multi-step organic reactions, allowing chemists to explore methods of creating new materials with desired functionalities. It emphasizes the creativity and skill involved in chemical synthesis.
- Electrochemical Properties: Compounds like 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione may possess interesting electrochemical properties, making them of interest in the study of conductive polymers and electrochemical sensors.
In summary, the study of 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione opens doors to understanding not just its role in biological systems, but also its potential technological applications. As Albert Einstein famously said, “The important thing is not to stop questioning. Curiosity has its own reason for existing.” Exploring these intriguing compounds fosters scientific curiosity and innovation.