Sipatrigine
- Molecular formula
- C16H10Cl2N2
- CAS Number
- 152946-68-4
- IUPAC Name
- N-(3,4-dichlorophenyl)-1-(1H-indol-3-yl)methanimine
- Molecular Weight
- 335.17g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4890g/cm3
- Synonyms
- (1E)-1-(3, 4-dichlorophenyl)-2-indol-3-yl-1-azaethene
Identification
Interesting Facts about N-(3,4-Dichlorophenyl)-1-(1H-indol-3-yl)methanimine
N-(3,4-Dichlorophenyl)-1-(1H-indol-3-yl)methanimine is a fascinating compound that represents a convergence of synthetic and natural chemistry. Here are some intriguing aspects of this molecule:
- Dual Nature: This compound features both chlorophenyl and indole moieties, showcasing the blending of synthetic and naturally occurring components.
- Biological Importance: Indole derivatives are well-known in biochemical research and have been identified as key players in various biological processes, including potential anti-cancer properties.
- Potential Applications: The structure of this compound may contribute to research in pharmaceuticals, particularly in the development of new therapeutic agents targeting diseases like cancer and infections.
- Research Interest: Given the strategic placement of the dichlorophenyl group, studies often explore how the substituents influence biological activity and molecular interactions.
- Mechanistic Studies: The compound's structure allows chemists to investigate reaction mechanisms and the effects of substituents on reactivity and stability.
Such compounds open up avenues for innovation in medicinal chemistry and materials science. As researchers delve deeper into its properties and potential implications, this compound could play a pivotal role in advancing our understanding of complex biological interactions.
In the words of a notable chemist, **"Each compound tells a story of molecular design and functional evolution."** This statement rings true for N-(3,4-Dichlorophenyl)-1-(1H-indol-3-yl)methanimine, which stands at the crossroads of chemistry, biology, and medicine.