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Identification

Molecular formula
C16H14N2O
CAS Number
842-07-9
IUPAC Name
4-(4-aminophenyl)azo-2,6-dimethyl-phenol
Molecular Weight
249.29g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1578g/cm3
Synonyms
21554-20-1
Interesting facts

Interesting Facts about 4-(4-aminophenyl)azo-2,6-dimethyl-phenol

4-(4-aminophenyl)azo-2,6-dimethyl-phenol, often simply referred to as a specific azo compound, is notable for its diverse applications and intriguing chemical properties. Here are some engaging insights into this fascinating molecule:

  • Azo Chemistry: This compound belongs to the class of azo compounds, which are characterized by the presence of the azo group (āˆ’N=Nāˆ’). Azo compounds are well-known for their vibrant colors and are widely used as dyes in various industries.
  • Synthetic Versatility: The synthetic route to creating this compound can be an exemplary illustration of azo coupling reactions. Azo dyes like this compound are formed by the reaction of a diazonium salt with a phenolic compound, which exemplifies key principles of organic synthesis.
  • Biological Relevance: A significant aspect of compounds like 4-(4-aminophenyl)azo-2,6-dimethyl-phenol is their potential biological activity. Certain azo compounds have been researched for their antimicrobial and anticancer properties, making them of interest in pharmaceutical applications.
  • Environmental Concerns: While these compounds have useful applications, their environmental impact and biodegradability are critical topics within chemical research. Studies have suggested that some azo dyes can degrade into potentially harmful amines, underscoring the importance of assessing their environmental fate.
  • Colorimetric Applications: The intensive color of azo compounds makes them essential in colorimetric analysis. This technique can be leveraged in analytical laboratories to quantify different substances in solution, showcasing the compound's practical applications in chemistry.

In summary, 4-(4-aminophenyl)azo-2,6-dimethyl-phenol serves as more than just a chemical formula. It represents a bridge between synthetic chemistry, practical applications in various fields, and ongoing research in green chemistry and toxicology. As we delve deeper into such compounds, we unlock the potential for innovation and discovery!

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