N-Ethylphthalimide

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Identification

Molecular formula
C10H9NO2
CAS Number
1841-30-3
IUPAC Name
2-ethylisoindoline-1,3-dione
Molecular Weight
189.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2195g/cm3
Synonyms
N-Ethylphthalimide
Interesting facts

Interesting Facts About 2-Ethylisoindoline-1,3-dione

2-Ethylisoindoline-1,3-dione is a fascinating compound that belongs to the family of isoindoline derivatives. These compounds have attracted considerable attention in recent years due to their unique structural properties and potential applications.

  • Structural Features: The structure of 2-ethylisoindoline-1,3-dione includes an isoindoline moiety, which contributes to its stability and reactivity. The presence of the ethyl group at the 2-position enhances its solubility and may influence its biological activities.
  • Biological Significance: Compounds like 2-ethylisoindoline-1,3-dione have been studied for their potential antimicrobial, anti-inflammatory, and even anticancer properties. This makes them of particular interest in medicinal chemistry.
  • Electron-Dense Environment: The presence of two carbonyl groups in the structure contributes to a rich electron-dense environment, which can facilitate various chemical reactions, including nucleophilic attacks and cycloadditions.
  • Synthetic Applications: The ability to synthesize derivatives of isoindoline-1,3-dione is valuable in creating new materials and pharmaceuticals. Chemists are continuously exploring different synthesis routes for functionalizing the isoindoline scaffold.
  • Fluorescent Properties: This compound has shown interesting fluorescent properties, making it beneficial in biological imaging and sensing applications, where visualization of cellular processes is essential.

In conclusion, 2-ethylisoindoline-1,3-dione is not just a simple compound; it stands as a testament to the intricate relationships between structure and function in chemistry. The ongoing research and exploration in the field may uncover even more exciting applications that harness its unique characteristics.

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