3-Butyl-3-phenylazetidin-2-one

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Identification

Molecular formula
C13H17NO
CAS Number
25599-02-6
IUPAC Name
3-butyl-3-phenyl-azetidin-2-one
Molecular Weight
203.28g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0944g/cm3
Synonyms
3-butyl-3-phenylazetidin-2-one
Interesting facts

Interesting Facts about 3-butyl-3-phenyl-azetidin-2-one

3-butyl-3-phenyl-azetidin-2-one is a fascinating compound that belongs to the class of azetidines, which are four-membered saturated heterocycles.

Unique Structural Features

This compound showcases several intriguing structural characteristics:

  • Azetidine Ring: The presence of the azetidine ring provides it with unique properties, making it a subject of interest in organic chemistry.
  • Substituents: The butyl and phenyl groups contribute to its chemical reactivity and potential applications in various fields.

Potential Applications

3-butyl-3-phenyl-azetidin-2-one also has notable applications:

  • Pharmaceuticals: Compounds containing the azetidine structure have been explored for their medicinal properties, including antifungal and anti-inflammatory activities.
  • Material Science: The structural integrity of azetidine derivatives may lend themselves to innovative materials with desirable mechanical properties.

Research and Synthesis

The synthesis of 3-butyl-3-phenyl-azetidin-2-one can be achieved through various organic reactions, which allows chemists to explore different synthetic pathways. This makes it an excellent compound for students and researchers looking to hone their organic synthesis skills:

  • Challenges in Synthesis: The construction of the azetidine ring often poses synthetic challenges, helping to cultivate problem-solving skills in chemists.
  • Insights into Reactivity: Studying this compound can provide insights into how substituents affect reactivity and stability within cyclic structures.

In summary, 3-butyl-3-phenyl-azetidin-2-one is more than just a simple molecule; its structure and potential applications open doors to a multitude of chemical explorations and innovations in both academic and industrial settings.

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