CCT129202
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- Molecular formula
- C16H9ClN2O4
- CAS Number
- 1196769-23-2
- IUPAC Name
- N-(4-chlorophenyl)-1,3-dioxo-4H-isoquinoline-4-carboxamide
- Molecular Weight
- 316.71g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5799g/cm3
- Synonyms
- TESICAM
Identification
Interesting facts
N-(4-chlorophenyl)-1,3-dioxo-4H-isoquinoline-4-carboxamide
N-(4-chlorophenyl)-1,3-dioxo-4H-isoquinoline-4-carboxamide is a fascinating compound that is notable for its diverse applications in medicinal chemistry. Here are some intriguing aspects of this compound:
- Biological Activity: This compound has attracted the attention of researchers for its potential pharmacological properties. Studies indicate that it may exhibit anti-inflammatory and anticancer activities, making it a candidate for future drug development.
- Diverse Functional Groups: The presence of the 4-chlorophenyl and 1,3-dioxo groups gives this compound a unique structure. The chlorinated aromatic ring can enhance the binding affinity to biological targets, possibly increasing its efficacy.
- Isoquinoline Framework: The isoquinoline skeleton is a well-known pharmacophore in many bioactive compounds. Its versatility allows for various modifications, making it a scaffold for generating a library of derivatives that can be tested for activity.
- Synthetic Pathways: The synthesis of this compound often involves advanced organic synthesis techniques, including condensation reactions and cyclization, showcasing the intricate methods used in modern organic chemistry.
- Research Potential: Ongoing studies are likely to explore the compound's mechanism of action and its interactions with cellular targets, which can lead to further insights into its therapeutic potential.
In summary, N-(4-chlorophenyl)-1,3-dioxo-4H-isoquinoline-4-carboxamide exemplifies the rich intersection of organic chemistry and pharmacology. As scientists continue to investigate its properties, this compound holds promise for contributing to advancements in therapeutic agents.