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bis(3,4-dimethylphenyl)diazene

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Identification
Molecular formula
C16H18N2
CAS number
57308-36-4
IUPAC name
bis(3,4-dimethylphenyl)diazene
State
State

At room temperature, bis(3,4-dimethylphenyl)diazene is typically in a solid state.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
392.16
Boiling point (Kelvin)
665.31
General information
Molecular weight
238.33g/mol
Molar mass
238.3300g/mol
Density
1.1137g/cm3
Appearence

Bis(3,4-dimethylphenyl)diazene appears as a solid compound, typically presenting in a crystalline form. It has a distinct coloration depending on its purity and crystalline form, which can range from yellow to orange.

Comment on solubility

Solubility of bis(3,4-dimethylphenyl)diazene

bis(3,4-dimethylphenyl)diazene, a diazene derivative, exhibits unique solubility characteristics that are influenced by its molecular structure. This compound is relatively insoluble in water, which is common among organic compounds with larger non-polar sections. However, it shows notable solubility in organic solvents. Here are some key points regarding its solubility:

  • Polar Solvents: Poor solubility due to the absence of polar functional groups.
  • Non-Polar Solvents: Soluble in solvents such as toluene and chloroform, which can successfully disrupt the molecular interactions of the compound.
  • Temperature Dependency: Increased temperature can enhance solubility in non-polar solvents.

Overall, the solubility behavior of bis(3,4-dimethylphenyl)diazene illustrates a classic example of the principle "like dissolves like," showcasing its preference for non-polar environments.

Interesting facts

Interesting Facts About Bis(3,4-dimethylphenyl)diazene

Bis(3,4-dimethylphenyl)diazene is a fascinating compound that showcases the diverse and intriguing nature of organic chemistry. Here are some notable aspects of this compound:

  • Structure and Function: This compound features a diazene functional group, which consists of a nitrogen-nitrogen double bond. This unique structure contributes to its reactivity and properties, making it a subject of interest for researchers.
  • Versatile Applications: Bis(3,4-dimethylphenyl)diazene plays a role in various fields, including organic synthesis and materials science. Its derivatives can be utilized in the development of dyes, pigments, and polymers.
  • Colorful Chemistry: Compounds like bis(3,4-dimethylphenyl)diazene can exhibit vibrant colors, which can be attributed to the conjugated system of double bonds present in its structure. This property makes it particularly interesting for applications in colorant production.
  • Potential in Research: Scientists are exploring bis(3,4-dimethylphenyl)diazene as a potential compound for use in photochemical studies due to its ability to absorb light and potentially undergo photochemical reactions.
  • Environmental Considerations: As with many synthetic compounds, understanding the environmental impact of bis(3,4-dimethylphenyl)diazene is crucial. Researchers are focused on evaluating its biodegradability and toxicity to ensure safe use in industrial applications.

In conclusion, bis(3,4-dimethylphenyl)diazene represents just one example of the complex and diverse world of organic compounds. Its unique properties and potential applications make it a valuable topic of investigation for chemists and materials scientists alike. As noted by chemists, "The journey of studying compounds like these reveals the endless possibilities within organic chemistry!"

Synonyms
29418-36-8
(e)-3,3',4,4'-tetramethylazobenzene
BIS(3,4-DIMETHYLPHENYL)DIAZENE
Eltrombopag Impurity 50
SCHEMBL11516839
SCHEMBL11516843
SCHEMBL31264508
1,2-Bis(3,4-dimethylphenyl)diazene