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2,6-Dimethoxyphenylphenyldiazene

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Identification
Molecular formula
C14H14N2O2
CAS number
53735-34-3
IUPAC name
(2,6-dimethoxyphenyl)-phenyl-diazene
State
State

This compound is a solid at room temperature. It is stable under normal conditions but should be protected from strong acids or bases which might cause it to decompose.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
240.27g/mol
Molar mass
240.2710g/mol
Density
1.1985g/cm3
Appearence

2,6-Dimethoxyphenylphenyldiazene typically appears as a crystalline solid with a yellow to orange color. It is often used in the preparation of azo dyes, which contribute to its vibrant appearance due to the azo group present in its structure.

Comment on solubility

Solubility of (2,6-dimethoxyphenyl)-phenyl-diazene

The solubility of (2,6-dimethoxyphenyl)-phenyl-diazene can be quite intriguing due to its unique molecular structure. Understanding the solubility of this compound involves considering a few critical factors:

  • Polarity: The presence of the methoxy groups can enhance the overall polarity of the molecule, impacting its solubility in various solvents.
  • Temperature: Like many organic compounds, solubility can increase with temperature. Heating a solvent can sometimes help dissolve more of the compound.
  • Solvent Type: This compound may exhibit different solubility characteristics in polar vs. non-polar solvents. Typically, **polar solvents** (like ethanol or acetone) could dissolve it better than **non-polar** ones (like hexane).

In general, it's key to remember that:

  1. **Like dissolves like**: The solubility of organic compounds is often dictated by the compatibility of their functional groups with solvent molecules.
  2. **Impurities and Concentration**: These factors can further influence solubility, making it vary significantly under different conditions.

As a result, while (2,6-dimethoxyphenyl)-phenyl-diazene may have limited solubility compared to more straightforward compounds, its interaction with solvents remains a fascinating area for exploration. Careful experimentation can unveil its potential usage in various applications involving organic synthesis and formulation.

Interesting facts

Interesting Facts about (2,6-Dimethoxyphenyl)-phenyl-diazene

(2,6-Dimethoxyphenyl)-phenyl-diazene, commonly known for its structural uniqueness, is a fascinating compound that attracts attention in various fields of chemistry. With its diazene functional group, this compound serves as a significant example of azo compounds, which are often characterized by their distinctive nitrogen-to-nitrogen double bond.

Key Highlights:

  • Application in Dyes: The compound can be a precursor in the synthesis of colorful azo dyes, which are widely used in textiles and inks due to their vibrant colors and stability.
  • Potential in Organic Electronics: Its molecular structure may show promise in organic electronics research, especially in the development of organic light-emitting diodes (OLEDs).
  • Research Opportunities: Scientists are interested in exploring its reactivity, as diazene derivatives can exhibit unique chemical behavior, leading to new derivatives with potential applications.
  • Thermodynamic Stability: The presence of the methoxy groups in its structure can enhance its stability, presenting interesting thermodynamic properties for study.

The study of (2,6-dimethoxyphenyl)-phenyl-diazene is not only interesting from a synthetic viewpoint, but it also opens doors to understanding the interplay between molecular structure and reactivity. As noted by researchers, "Every compound carries a story hidden within its atoms, waiting to be unveiled through diligent study and exploration." This emphasizes the importance of delving deep into the realm of molecular chemistry.

In summary, (2,6-dimethoxyphenyl)-phenyl-diazene is a compound that not only stands out due to its unique composition but also engages the scientific community in discussions of its potential applications and underlying chemical principles. Its exploration not only furthers our understanding of azo compounds but also inspires new innovations in materials science.

Synonyms
2,6-DIMETHOXYAZOBENZENE
29418-48-2
SCHEMBL3290173
SCHEMBL3290174