Indolinone derivative
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- Molecular formula
- C18H15ClN2O
- CAS Number
- Not available
- IUPAC Name
- 5-chloro-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylene]indolin-2-one
- Molecular Weight
- 312.78g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4500g/cm3
- Synonyms
- su5614
Identification
Interesting facts
Interesting Facts about 5-chloro-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylene]indolin-2-one
5-chloro-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylene]indolin-2-one is a remarkable compound belonging to the indole class of organic compounds, widely studied for its diverse biological properties. Here are some intriguing aspects of this compound:
- Diverse Applications: This compound has attracted attention in medicinal chemistry due to its potential applications in drug development, particularly as a scaffold for creating new pharmaceuticals.
- Biological Significance: Indolinones, such as this compound, are often investigated for their anticancer properties and ability to inhibit various enzymes. Researchers explore their capabilities to treat different malignancies.
- Structure-Activity Relationships: The inclusion of the 3,5-dimethyl-1H-pyrrol-2-yl group in its structure complicates the analysis of how such modifications affect biological activity. Scientists often utilize structure-activity relationship (SAR) studies to understand these influences better.
- Chlorine's Role: The presence of chlorine in its molecular structure plays a crucial role in enhancing the compound's lipophilicity, which can improve its biological activity by facilitating cellular uptake.
- Research Potential: Continued research is vital for discovering new properties, exploring synthesis methods, and finding innovative uses in the fields of pharmaceuticals and agrochemicals.
This compound epitomizes the intersection of organic chemistry and pharmacology, encouraging chemists to explore uncharted territories of molecular biology and medicinal uses while emphasizing the significance of small structural changes on biological functionality.