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Disperse Orange 11

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Identification
Molecular formula
C9H4BrClN4
CAS number
82-28-0
IUPAC name
2-(4-bromo-2-chloro-phenyl)azopropanedinitrile
State
State

At room temperature, Disperse Orange 11 is in a solid state.

Melting point (Celsius)
242.00
Melting point (Kelvin)
515.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
321.51g/mol
Molar mass
321.5400g/mol
Density
1.6700g/cm3
Appearence

Disperse Orange 11 is an orange crystalline powder.

Comment on solubility

Solubility of 2-(4-bromo-2-chloro-phenyl)azopropanedinitrile

2-(4-bromo-2-chloro-phenyl)azopropanedinitrile is an intriguing compound with unique solubility characteristics. When exploring its solubility, several factors come into play:

  • Polarity: The presence of multiple functional groups, particularly nitrile groups, influences its polarity. This can affect how well the compound dissolves in different solvents.
  • Solvent Choices: Common solvents like water may show limited solubility due to the compound's hydrophobic characteristics. On the other hand, organic solvents such as acetone or ethanol might enhance dissolvability.
  • Temperature Effects: As with many organic compounds, increasing the temperature can elevate solubility levels, allowing more of the compound to dissolve.
  • Concentration Factors: At higher concentrations, one may observe a saturation point that could limit further dissolution.

In summary, the solubility of 2-(4-bromo-2-chloro-phenyl)azopropanedinitrile can be influenced by its polarity, the choice of solvent, temperature adjustments, and concentration levels. Understanding these factors is crucial for effective applications in chemical processes.

Interesting facts

Interesting Facts about 2-(4-bromo-2-chloro-phenyl)azopropanedinitrile

2-(4-bromo-2-chloro-phenyl)azopropanedinitrile, a fascinating organic compound, serves as a prime example of modern synthetic chemistry. This compound features a complex structure that showcases the intricacies of aromatics and nitriles, leading to numerous applications in various fields.

Key Highlights

  • Synthetic Potential: The construction of this compound involves innovative methods of coupling reactions, exemplifying the power of synthetic organic chemistry.
  • Applications: Due to its distinctive structure, it can be utilized in material science, especially in the development of polymers and dyes.
  • Biological Activity: Compounds with similar structures have been studied for their antimicrobial and antifungal properties, suggesting potential therapeutic applications.

In the realm of chemistry education, this compound can be particularly valuable for students, as it serves as a case study in functional group analysis and reaction mechanisms. The presence of both bromo and chloro substituents allows for discussions surrounding nucleophilic substitution reactions and electrophilic aromatic substitution.

Importance in Research

In research laboratories, the utility of 2-(4-bromo-2-chloro-phenyl)azopropanedinitrile extends beyond academics; it can be instrumental in the design of new compounds that may lead to breakthroughs in various chemical industries. As scientists continue to explore its properties, this compound is expected to reveal even more intriguing facets of its chemistry.

By understanding compounds like this, researchers can pave the way for future innovations that harness the potential of chemistry to solve real-world problems. The ongoing quest for understanding the mechanisms and modifications of such compounds keeps the field dynamic and exciting.

Synonyms
((4-Bromo-2-chlorophenyl)azo)malononitrile
6017-38-5
2-Chlor-4-brom-phenyl-azo-malonitril [German]
2-Chlor-4-brom-phenyl-azo-malonitril
MALONONITRILE, ((4-BROMO-2-CHLOROPHENYL)AZO)-