Hexogen

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Identification

Molecular formula
C3H6N6O6
CAS Number
121-82-4
IUPAC Name
1-(3,5-dinitro-1,3,5-triazinan-1-yl)ethanone
Molecular Weight
222.12g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.8060g/cm3
Synonyms
14168-42-4
Interesting facts

Interesting Facts about 1-(3,5-Dinitro-1,3,5-triazinan-1-yl)ethanone

The compound 1-(3,5-dinitro-1,3,5-triazinan-1-yl)ethanone is a noteworthy member of the triazine family, known for its unique structure and potential applications in various fields of chemistry.

Key Features:

  • Composition: This compound contains a triazine ring that is substituted with nitro groups, contributing to its reactivity and stability.
  • Applications: The presence of dinitro groups often indicates potential uses in explosives or as intermediates in chemical syntheses.
  • Research Interest: Scientists are particularly interested in its *electronic properties*, as the nitro groups can affect the compound’s behavior in different chemical reactions.

Chemical Behavior:

The incorporation of nitro groups within the triazine framework enhances the electron-withdrawing capability of the compound, which can lead to increased acidity and reactivity in nucleophilic substitution reactions. This property makes it a valuable subject of study for identifying new synthetic pathways.

Quote from Researchers:

“Understanding the versatile behavior of compounds like 1-(3,5-dinitro-1,3,5-triazinan-1-yl)ethanone opens doors to innovative applications in materials science and beyond.”

In summary, 1-(3,5-dinitro-1,3,5-triazinan-1-yl)ethanone exemplifies the intricate relationship between molecular structure and chemical reactivity, making it a compelling focus of ongoing research in chemical science.

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