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- Molecular formula
- C16H10N2O2
- CAS Number
- 482-89-3
- IUPAC Name
- 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide
- Molecular Weight
- 262.27g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4000g/cm3
Identification
Interesting facts
Interesting Facts About 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide
The compound 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide exhibits fascinating properties and potential applications in scientific research. Here are some intriguing aspects of this compound:
- Indole Framework: This compound features a unique indole structure, a bicyclic compound known for its presence in many natural products and pharmaceuticals. Indole derivatives have been recognized for their biological activities, including anticancer, anti-inflammatory, and antimicrobial properties.
- Vinyl Group Influence: The presence of a vinyl group is significant as it can influence the compound's reactivity and stability. This structural motif can facilitate various chemical reactions and has implications for drug design and synthesis.
- Potential in Drug Discovery: Due to its unique structure, this compound could serve as a promising candidate in the realm of drug discovery, especially in targeting specific biological pathways associated with diseases.
- Chemical Versatility: The compound can undergo various transformations that make it suitable for implementing in synthetic organic chemistry, leading to diverse derivatives and analogs that may have enhanced activity or selectivity.
- Research Interest: Researchers have expressed keen interest in exploring compounds with indole motifs for their potential use in treating complex diseases, encouraging ongoing studies in medicinal and organic chemistry.
In conclusion, 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide serves as a prime example of how chemical structure intertwines with biological function, supporting the continuous pursuit of new therapeutic agents in the field of medicinal chemistry.