Skip to main content

Phenylazo mesitylene

ADVERTISEMENT
Identification
Molecular formula
C15H16N2
CAS number
2100-43-8
IUPAC name
phenyl-(2,4,6-trimethylphenyl)diazene
State
State

At room temperature, phenylazo mesitylene is in a solid state. It forms well-defined crystals due to its aromatic structure and intermolecular forces. This solid state is maintained until it reaches its melting point.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
331.00
Boiling point (Kelvin)
604.15
General information
Molecular weight
224.32g/mol
Molar mass
224.3190g/mol
Density
0.9811g/cm3
Appearence

Phenylazo mesitylene typically appears as a red or orange crystalline solid. It is known for its vibrant color, which stems from π-conjugated systems within its structure. The intensity of the color typically makes it easily identifiable in its pure form.

Comment on solubility

Solubility of Phenyl-(2,4,6-trimethylphenyl)diazene

The solubility of the compound phenyl-(2,4,6-trimethylphenyl)diazene can be an intriguing subject of exploration. Understanding its solubility characteristics not only aids in its practical applications but also enhances our knowledge of its chemical behavior in various environments.

General Solubility Characteristics:

  • Solvent Dependence: The solubility of this diazene compound is significantly influenced by the choice of solvent. It tends to be more soluble in organic solvents than in water.
  • Hydrophobic Nature: Given its aromatic structure, the compound exhibits hydrophobic characteristics, which means it does not readily dissolve in polar solvents like water.
  • Nonpolar Solvents: It shows an increased solubility in nonpolar solvents such as hexane or benzene due to its similar nonpolar features.

In summary, phenyl-(2,4,6-trimethylphenyl)diazene displays limited solubility in aqueous solutions and demonstrates greater solubility in organic solvents, reflecting its hydrophobic tendencies. This behavior is crucial in contexts where the compound may be used, as it can affect its reactivity and interactions with other substances.

Interesting facts

Interesting Facts about Phenyl-(2,4,6-Trimethylphenyl)Diazene

Pheyl-(2,4,6-trimethylphenyl)diazene, often referred to in the scientific community for its unique structural attributes and potential applications, is a fascinating compound to study. Here are some highlights:

  • Diazene Framework: This compound features a diazene functionality, which contains a nitrogen-nitrogen double bond. Diazene compounds are known for their unique reactivity and versatility in organic synthesis.
  • Stability and Reactivity: The presence of the phenyl and trimethylphenyl groups contributes to the overall stability of the molecule while also influencing its reactivity patterns. This combination can make it useful in various synthetic pathways.
  • Applications:
    • Could serve as a valuable intermediate in the synthesis of dyes and pigments due to its chromophoric character.
    • Might also find applications in the development of *photoresponsive materials*, potentially enhancing the performance of organic photonic devices.
  • Research Interest: Chemists are particularly intrigued by compounds like phenyl-(2,4,6-trimethylphenyl)diazene due to their potential role in catalysis and as building blocks for more complex molecular architectures.

To quote one of the notable chemists in the field, "The potential of diazene compounds lies not only in their structural beauty but also in their capability to participate in transformative chemical processes." With ongoing research, this compound continues to demonstrate its significance in advancing the science of organic chemistry beyond initial expectations.

Understanding the properties and reactions of phenyl-(2,4,6-trimethylphenyl)diazene not only enriches our knowledge of nitrogen-containing compounds but also encourages innovative approaches in material science.

Synonyms
2,4,6-TRIMETHYLAZOBENZENE
29418-26-6
SCHEMBL3285225
SCHEMBL3285227