2-allyl-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide

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Identification

Molecular formula
C11H9ClN2O5S
CAS Number
57720-77-5
IUPAC Name
2-allyl-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide
Molecular Weight
315.72g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5300g/cm3
Synonyms
BRN 0431191
Interesting facts

Interesting Facts about 2-allyl-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide

2-allyl-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide is a fascinating compound that belongs to the isoindoline family, which is renowned for its varied biological activities and applications in medicinal chemistry. Below are some compelling aspects of this compound:

  • Diverse Applications: This compound has shown potential in various fields, primarily as a pharmaceutical agent. Researchers are investigating its capabilities in targeting specific biological pathways, making it a candidate for future drug development.
  • Structure-Activity Relationship: The unique structure of 2-allyl-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide allows it to interact with biological systems in distinctive ways. The presence of the sulfonamide group is particularly noteworthy, as sulfonamides are widely recognized for their antibacterial properties.
  • Chloro Substituent: The 6-chloro substitution is crucial for the compound's reactivity and ability to form interactions with target proteins. Chlorine atoms can significantly influence the lipophilicity and electronic characteristics of compounds, which in turn affects their biological activity.
  • Potential as a Therapeutic Agent: Preliminary studies on similar compounds suggest that derivatives may exhibit anti-inflammatory and anticancer properties. As research progresses, the therapeutic potential of this compound may unravel new opportunities in drug design.
  • Innovative Synthesis: The synthetic methods to obtain this compound can involve various strategies, including multi-step organic synthesis techniques. This offers chemistry students and researchers a chance to explore advanced synthetic methodologies in organic chemistry.

Furthermore, the study of 2-allyl-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide not only enriches our understanding of synthetic organic compounds but also highlights the importance of interdisciplinary research in addressing complex biological challenges. As chemists continue to explore this intriguing compound, who knows what groundbreaking discoveries await!

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