3,5-Lutidine N-oxide

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Identification

Molecular formula
C7H9NO
CAS Number
1003-75-2
IUPAC Name
3,5-dimethyl-1-oxido-pyridin-1-ium
Molecular Weight
125.16g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0500g/cm3
Synonyms
3, 5-dimethylpyridin-1-ium-1-olate
Interesting facts

Interesting Facts about 3,5-Dimethyl-1-oxido-pyridin-1-ium

The compound 3,5-dimethyl-1-oxido-pyridin-1-ium is a fascinating molecule that falls within the realm of heterocyclic compounds. This particular structure is characterized by a pyridine ring, which is notable for its aromatic properties and electron-withdrawing characteristics. Here are some intriguing points about this compound:

  • Structural Features: The presence of the oxido group (–O) introduces unique reactivity, enabling it to participate in various chemical transformations.
  • Biological Activity: Compounds containing pyridine rings often exhibit interesting biological activities. In research, they may be investigated for their potential as pharmaceuticals.
  • Applications: This compound may serve as a precursor or intermediate in the synthesis of more complex molecules, which can be used in the development of agrochemicals or pharmaceuticals.
  • Electronic Properties: The dimethyl substitutions enhance the electron density on the pyridine nitrogen, potentially altering its reactivity and making it a good candidate for coordination with metal ions.

The versatility of the 3,5-dimethyl-1-oxido-pyridin-1-ium compound demonstrates its importance in both synthetic and industrial chemistry. As noted by chemists, "The study of heterocycles opens up numerous pathways for discovering new compounds with valuable properties." This highlights the significance of compounds like 3,5-dimethyl-1-oxido-pyridin-1-ium in advancing science and technology.

In summary, the intriguing structure and properties of 3,5-dimethyl-1-oxido-pyridin-1-ium make it a subject of considerable interest in both academic research and practical applications.

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