Fentanyl

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Identification

Molecular formula
C22H28N2O1
CAS Number
437-38-7
IUPAC Name
2-(diethylamino)ethyl 3-(2-furyl)-2-(1-naphthyl)propanoate
Molecular Weight
336.48g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3150g/cm3
Synonyms
3216-74-8
Interesting facts

Interesting Facts about 2-(diethylamino)ethyl 3-(2-furyl)-2-(1-naphthyl)propanoate

This compound belongs to the class of esthers and is notable for its potential applications in various pharmaceutical contexts. The unique combination of functional groups in its structure opens up several intriguing avenues for research and development.

Key Features

  • The Furyl Group: The presence of the furyl moiety contributes to the compound's aromatic character, which may enhance its interactions with biological targets. Furan derivatives are known for their diverse biological activities.
  • Naphthyl Component: The inclusion of the naphthyl group provides additional stability and can potentially improve the lipophilicity of the compound, which affects its pharmacokinetic properties.
  • Diethylamino Functionality: The diethylamino group is often linked with enhanced nucleophilicity, which may facilitate various chemical reactions or enhance binding affinity in biological systems.

Researchers find compounds like this particularly interesting due to their ability to interact with specific receptors or enzymes, paving the way for the development of novel therapeutic agents. Moreover, the intricate structure-activity relationship provides a rich area for investigation, allowing chemists to modify different portions of the molecule to optimize its biological activity.

In summary, the molecular architecture of 2-(diethylamino)ethyl 3-(2-furyl)-2-(1-naphthyl)propanoate makes it a fascinating compound with potential in medicinal chemistry, offering an intersection of synthetic organic chemistry and pharmacology. As always, careful research is essential to elucidate its full potential!

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