Vesnarinone

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Identification

Molecular formula
C22H33ClN2O4
CAS Number
81840-15-5
IUPAC Name
2-(2-butanoyl-6-nitro-phenoxy)ethyl-diisopropyl-ammonium;chloride
Molecular Weight
462.01g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1234g/cm3
Synonyms
Butyrophenone, 6'-(2-(diisopropylamino)ethoxy)-5'-nitro-, hydrochloride
Interesting facts

Interesting Facts About 2-(2-butanoyl-6-nitro-phenoxy)ethyl-diisopropyl-ammonium;chloride

This unique compound, 2-(2-butanoyl-6-nitro-phenoxy)ethyl-diisopropyl-ammonium chloride, is a fascinating example of how modifications in chemical structure can lead to significant changes in properties and applications. Here are some captivating points about this compound:

  • Versatile Structure: The inclusion of a butanoyl group along with a nitrophenyl moiety makes this compound particularly interesting. This combination can influence its chemical reactivity and potential biological activity.
  • Potential Biological Applications: Many compounds with similar amine structures are investigated for their use in pharmaceuticals, often acting as ion channel modulators or affecting neurotransmitter systems.
  • Ammonium Compounds: As a quaternary ammonium compound, it possesses a permanently charged ammonium center, which can enhance its solubility in polar solvents and possibly affect its interaction with biomolecules.
  • Research Interest: The nitro group is known for its reactivity, making this compound a potential candidate for further studies in chemical synthesis or medicinal chemistry.
  • Environmental Considerations: The study of chlorinated compounds is paramount, given their diverse functionalities but also their implications in environmental chemistry, particularly regarding stability and biodegradability.

In summary, the compound 2-(2-butanoyl-6-nitro-phenoxy)ethyl-diisopropyl-ammonium chloride represents a convergence of structural complexity and potential, making it a compelling subject of study in both organic and medicinal chemistry. Its unique attributes might unlock novel pathways for therapeutic advancements.

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