(2,6-dimethoxyphenyl)-(o-tolyl)diazene

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Identification

Molecular formula
C15H16N2O2
CAS Number
4744-51-2
IUPAC Name
(2,6-dimethoxyphenyl)-(o-tolyl)diazene
Molecular Weight
240.30g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2100g/cm3
Synonyms
2, 6-DIMETHOXY-2'-METHYLAZOBENZENE
Interesting facts

Interesting Facts about (2,6-dimethoxyphenyl)-(o-tolyl)diazene

(2,6-dimethoxyphenyl)-(o-tolyl)diazene is a fascinating compound that falls under the category of diazenes, which are characterized by a nitrogen-nitrogen double bond. This compound showcases a variety of intriguing features that make it a subject of interest in the field of organic chemistry.

Chemical Structure and Stability

Its unique structure includes:

  • Two aromatic rings: The presence of the 2,6-dimethoxyphenyl and o-tolyl groups enhances the compound's stability.
  • Electron-donating groups: The methoxy groups contribute significantly to the electron density, influencing the compound's reactivity.
  • Diverse isomerism: The arrangement of the phenyl and toluidine components allows for potential isomeric forms.

Applications in Research

This compound is not just a mere chemical entity; it holds considerable potential in various applications:

  • Organic Synthesis: It can serve as a building block for synthesizing more complex chemical structures.
  • Material Science: The stability and properties of diazenes make them suitable for developing new materials.
  • Pharmaceuticals: Investigations into diazene derivatives often explore their biological activity, showing promise in drug development.

Significance in Chemistry

It is essential to note that diazenes, in general, play a vital role in:

  • Redox Reactions: The nitrogen-nitrogen bond can behave as a reducing agent, participating in various chemical reactions.
  • Research on Azo Compounds: As diazenes are closely related to azo compounds, studying them contributes to understanding azo dye chemistry.
  • Functionalization: The functional groups present open avenues for further chemical modifications, leading to new derivatives with varied properties.

In summary, (2,6-dimethoxyphenyl)-(o-tolyl)diazene stands out due to its unique chemical characteristics and potential applications. As we continue unraveling the mysteries surrounding such compounds, they will undoubtedly contribute to advances in chemical research and applications.

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