Aminophenazone

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Identification

Molecular formula
C13H17N3O
CAS Number
58-15-1
IUPAC Name
4-amino-1,5-dimethyl-2-phenyl-pyrazol-3-one
Molecular Weight
231.30g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1870g/cm3
Synonyms
4-Aminoantipyrine
Interesting facts

Exploring 4-amino-1,5-dimethyl-2-phenyl-pyrazol-3-one

4-amino-1,5-dimethyl-2-phenyl-pyrazol-3-one is a fascinating compound that belongs to the class of pyrazolone derivatives. This compound not only showcases unique chemical properties but also finds various applications in different fields of science.

Key Highlights:

  • Structure and Stability: The presence of the pyrazolone ring gives this compound its characteristic stability and reactivity, making it an important scaffold in organic synthesis.
  • Biological Relevance: Compounds of this class have been studied for their potential pharmacological properties, including anti-inflammatory and analgesic effects. They might serve as candidates for developing new medicinal agents.
  • Synthetic Versatility: The synthetic pathways leading to this compound are particularly interesting; chemists often tweak the structure for improved activity or selectivity, showcasing the adaptability of organic synthesis techniques.
  • Research Applications: In the field of materials science, derivatives of 4-amino-1,5-dimethyl-2-phenyl-pyrazol-3-one are being explored for usage in dyes, pigments, and other functional materials.

Overall, 4-amino-1,5-dimethyl-2-phenyl-pyrazol-3-one stands out as a compound of great interest to both synthetic chemists and pharmacologists alike. As research continues, the potential applications and derivatives stemming from this unique pyrazolone may lead to important breakthroughs in various scientific domains. As one researcher aptly stated, "The beauty of organic synthesis lies in its limitless potential to innovate."

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