Clorotepine acetate
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- Molecular formula
- C21H15ClN4O5S
- CAS Number
- 10556-72-4
- IUPAC Name
- 6-chloro-N-[4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl]-4-oxo-chromene-2-carboxamide
- Molecular Weight
- 433.88g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4000g/cm3
- Synonyms
- BRN 0949209
Identification
Interesting facts
Interesting Facts about 6-Chloro-N-[4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl]-4-oxo-chromene-2-carboxamide
6-Chloro-N-[4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl]-4-oxo-chromene-2-carboxamide is a fascinating compound that belongs to a class of organic molecules with unique properties and applications. Here are some intriguing insights:
- Pharmaceutical Potential: This compound has garnered interest in medicinal chemistry due to its structural features, which may provide insights into the design of new pharmaceuticals.
- Structural Diversity: The combination of the chromene moiety with sulfamoyl and pyrimidine groups contributes to its potential to interact with biological targets in diverse ways.
- Synthesis Pathways: The synthesis of such complex compounds often involves multiple reaction steps, showcasing the creativity and innovation required in synthetic organic chemistry.
- Biological Activity: Research into sulfonamide derivatives, to which this compound is related, suggests potential antibacterial and antitumor activities, making it a promising candidate for further studies.
- Mechanistic Insights: Understanding how this compound interacts at the molecular level with biological systems can provide insights into its efficacy and safety profile as a therapeutic agent.
In conclusion, 6-chloro-N-[4-[(4-methylpyrimidin-2-yl)sulfamoyl]phenyl]-4-oxo-chromene-2-carboxamide epitomizes the intricate relationship between chemical structure and biological activity. As a student or scientist delving into the realm of organic compounds, this molecule serves as an excellent example of the innovative strategies employed in drug discovery.