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Azo-anisole

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Identification
Molecular formula
C14H14N2O2
CAS number
1635-42-1
IUPAC name
(2,4-dimethoxyphenyl)-phenyl-diazene
State
State

At room temperature, Azo-anisole is a solid.

Melting point (Celsius)
36.00
Melting point (Kelvin)
309.15
Boiling point (Celsius)
344.00
Boiling point (Kelvin)
617.15
General information
Molecular weight
242.28g/mol
Molar mass
242.2750g/mol
Density
1.0970g/cm3
Appearence

Azo-anisole appears as a crystalline solid with a characteristic yellow-orange color.

Comment on solubility

Solubility of (2,4-Dimethoxyphenyl)-phenyl-diazene

(2,4-Dimethoxyphenyl)-phenyl-diazene, a complex organic compound, exhibits varying solubility characteristics depending on the solvent employed. Understanding its solubility is integral to its application in chemical processes. Here are some key points regarding its solubility:

  • Polarity: The presence of the dimethoxy groups suggests moderate polarity, which may enhance solubility in polar solvents.
  • Solvent Compatibility: This compound may dissolve better in organic solvents such as:
    • Ethyl acetate
    • Chloroform
    • DMSO (Dimethyl sulfoxide)
  • Water Solubility: Generally, organic compounds with similar structures have low solubility in water due to non-polar character overshadowing polarity.
  • Temperature Effects: Solubility can increase with temperature, which may provide a better dissolution in organic solvents.

In summary, the solubility profile of (2,4-dimethoxyphenyl)-phenyl-diazene is influenced by both its molecular structure and the nature of the solvent. As such, it is vital to experiment with different solvents to achieve optimal solubility for specific applications.

Interesting facts

Interesting Facts about (2,4-dimethoxyphenyl)-phenyl-diazene

(2,4-dimethoxyphenyl)-phenyl-diazene is a fascinating compound that belongs to the class of azo compounds, which are known for their striking colors and diverse applications in various fields. Here are some intriguing aspects of this compound:

  • Azo Compounds: The azo group (>N=N<) is a defining feature of this compound and is responsible for its potential vibrant color. Azo compounds are widely used as dyes and pigments in textiles, food, and cosmetics.
  • Substituents Matter: The presence of two methoxy groups in the 2 and 4 positions of the phenyl ring significantly influences the compound's reactivity and stability. These electron-donating groups enhance the compound's ability to absorb light.
  • Applications: Beyond their visual appeal, compounds like (2,4-dimethoxyphenyl)-phenyl-diazene show promise in materials science for creating sensors and organic electronic devices. Their ability to shift electronic properties through structural modification opens doors for innovative applications.
  • Biological Interest: Some azo compounds exhibit antimicrobial and antitumor properties, making them objects of interest in pharmaceuticals and agricultural science. The study of their biological effects is an active area of research.
  • Environmental Impact: The dye industry faces scrutiny regarding the environmental impact of azo dyes. Understanding the degradation pathways of these compounds is crucial for developing sustainable practices and minimizing pollution.

In summary, (2,4-dimethoxyphenyl)-phenyl-diazene is not merely a chemical entity but a compound with rich implications in chemistry, materials science, and environmental studies. Its unique properties stemming from its azo structure invite both curiosity and rigorous scientific exploration.

Synonyms
2,4-DIMETHOXYAZOBENZENE
29418-46-0
SCHEMBL3287372
SCHEMBL3287376
(E)-1-(2,4-dimethoxyphenyl)-2-phenyldiazene