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(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
State
State

At room temperature, (2,6-dimethoxyphenyl)-(o-tolyl)diazene is predominantly in a solid state. It is typically found as a crystalline powder, allowing for relatively easy handling and storage. Its azo group structure impacts its stability and color characteristics under standard laboratory conditions.

Melting point (Celsius)
131.50
Melting point (Kelvin)
404.65
Boiling point (Celsius)
430.00
Boiling point (Kelvin)
703.15
General information
Molecular weight
240.30g/mol
Molar mass
240.2780g/mol
Density
1.2100g/cm3
Appearence

(2,6-dimethoxyphenyl)-(o-tolyl)diazene is usually a solid compound at room temperature, and it generally displays a crystalline or powder-like appearance. The color of this compound can vary, but it is often observed as a light yellow substance, characteristic of many azo compounds due to the presence of the azo group (N=N).

Comment on solubility

Solubility of (2,6-Dimethoxyphenyl)-(o-tolyl)diazene

The solubility of (2,6-dimethoxyphenyl)-(o-tolyl)diazene can be quite intriguing and is influenced by its molecular structure. Given the presence of both methoxy and phenyl groups, which are relatively non-polar, this compound's solubility behavior in different solvents is notable:

  • In Organic Solvents: This compound is likely to be more soluble in non-polar organic solvents such as toluene or dichloromethane due to its hydrophobic character.
  • In Aqueous Solutions: However, its solubility in water is expected to be very low, as the hydrophilic interactions are limited by the bulkiness of the aromatic rings and the methoxy groups.
  • Effect of Temperature: The solubility may increase with temperature, as is common for many organic compounds, but substantial solubilization in water is still improbable.

In summary, it can be said that:

"The solubility of organic compounds often reflects their structural and electronic characteristics."

Thus, while (2,6-dimethoxyphenyl)-(o-tolyl)diazene shows favorable solubility in organic environments, its presence in aqueous solutions remains minimal.

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.

Synonyms
2,6-DIMETHOXY-2'-METHYLAZOBENZENE
29418-51-7