Biphenylquinone

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Identification

Molecular formula
C20H21NO2
CAS Number
91-23-6
IUPAC Name
3-(1,1-dimethylallyl)-3-(4-methylpent-3-enyl)-1H-quinoline-2,4-dione
Molecular Weight
311.40g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3027g/cm3
Synonyms
NSC692276
Interesting facts

Interesting Facts about 3-(1,1-dimethylallyl)-3-(4-methylpent-3-enyl)-1H-quinoline-2,4-dione

This fascinating compound, a member of the quinoline family, presents a variety of intriguing features that remind us of the complexity and beauty of organic chemistry:

  • Quinoline Backbone: The structure of this compound is notably defined by the quinoline ring system, which is known for its role in various biological activities. This backbone is essential in developing pharmaceuticals due to its presence in numerous bioactive molecules.
  • Diverse Applications: Compounds like this one have been studied for their potential as:
    • Antimicrobial agents
    • Anticancer drugs
    • Anti-inflammatory agents
  • Synthetic Routes: The synthesis of complex compounds often involves multi-step processes that showcase the creativity of chemists. For this compound, techniques such as allylic functionalization may be applied to build the intricate structure.
  • Structure-Activity Relationship (SAR): Researchers study how changes in the chemical structure influence biological activity. This compound demonstrates how substituents like the dimethylallyl and 4-methylpent-3-enyl groups can significantly affect the pharmacological profile.
  • Natural Occurrence: Quinoline derivatives are often found in nature, sometimes in plants or as products of bacterial metabolism, highlighting their ecological importance.

In conclusion, the study of 3-(1,1-dimethylallyl)-3-(4-methylpent-3-enyl)-1H-quinoline-2,4-dione opens doors to understanding not only its chemical properties but also its potential utility in medicinal chemistry. As the field continues to evolve, the future may reveal even more applications for this remarkable compound.

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