NTO (3-nitro-1,2,4-triazol-5-one)

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Identification

Molecular formula
C9H7N5O2
CAS Number
950-37-8
IUPAC Name
6-(3-nitrophenyl)-1,3,5-triazine-2,4-diamine
Molecular Weight
218.17g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.7280g/cm3
Synonyms
2, 4-Diamino-6-(3-nitrophenyl)-1, 3, 5-triazine
Interesting facts

Interesting Facts About 6-(3-Nitrophenyl)-1,3,5-triazine-2,4-diamine

6-(3-Nitrophenyl)-1,3,5-triazine-2,4-diamine is a fascinating compound that showcases the intriguing world of triazine derivatives. Here are some compelling points about this compound:

  • Structural Complexity: This compound features a triazine ring, which is a six-membered aromatic heterocycle. The presence of nitro and amino groups contributes to its diverse chemical properties and potential functionalities.
  • Applications in Dye Chemistry: Triazine derivatives, including this compound, are often utilized in the field of dye chemistry. They can serve as precursors for the synthesis of various colorants, especially in textiles and inks.
  • Biological Activity: The nitrophenyl group is known for imparting biological activities to compounds. This feature makes 6-(3-Nitrophenyl)-1,3,5-triazine-2,4-diamine a subject of interest in pharmaceuticals, particularly in the development of anti-cancer agents and herbicides.
  • Stability: The stability of triazine compounds in various conditions is remarkable. This property can be attributed to the resonance structures that stabilize the triazine core, making it resistant to degradation.
  • Synthetic Routes: Chemists have developed various synthetic pathways to create this compound. These methods typically involve nucleophilic substitutions and functional group transformations that underscore the versatility of triazine chemistry.
  • Analytical Techniques: The investigation of 6-(3-Nitrophenyl)-1,3,5-triazine-2,4-diamine often requires advanced analytical techniques such as NMR, IR spectroscopy, and mass spectrometry to fully characterize its structure and properties.

In summary, 6-(3-Nitrophenyl)-1,3,5-triazine-2,4-diamine represents a captivating example of triazine chemistry, revealing its potential in various fields including dye production and medicinal chemistry. As scientists continue to explore its applications, its significance in chemical research remains ever-growing.

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