2-methyl-3,5-dinitrobenzamide

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Identification

Molecular formula
C8H7N3O4
CAS Number
0
IUPAC Name
2-methyl-3,5-dinitro-benzamide
Molecular Weight
211.15g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4570g/cm3
Synonyms
dinitolmide
Interesting facts

Interesting Facts About 2-Methyl-3,5-Dinitro-Benzamide

2-Methyl-3,5-dinitro-benzamide is an intriguing compound known for its diverse applications in various fields. Here are some fascinating insights into this compound:

  • Structure and Reactivity: The compound features a benzamide backbone, which is further substituted with two nitro groups and a methyl group. This unique structure contributes to its reactivity, especially in electrophilic aromatic substitution reactions.
  • Applications in Research: 2-Methyl-3,5-dinitro-benzamide has gained attention as a reagent in organic synthesis, particularly when exploring new pharmaceuticals and agrochemicals. Its derivatives can exhibit varied biological activities, making it valuable in medicinal chemistry.
  • Explosive Potential: Due to the presence of nitro groups, this compound may also possess explosive characteristics under specific conditions. Nitro-substituted compounds are often studied for their potential use in explosives and propellants, highlighting the importance of safety protocols when handling them.
  • Biological Impact: Some studies have indicated that compounds with similar structures can interact with biological systems, showcasing potential anti-cancer properties. Research is ongoing to understand the mechanisms by which they may influence cellular processes.
  • Environmental Considerations: Like many nitrogen-containing compounds, there can be environmental implications associated with their production and degradation. Understanding how 2-Methyl-3,5-dinitro-benzamide breaks down in nature is essential for assessing its ecological footprint.

In summary, 2-methyl-3,5-dinitro-benzamide is a compound rich in both chemical intrigue and practical applications, representing the fascinating interplay between structure and function in organic chemistry.

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