Hexogen
- 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
Identification
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.