Pyrazole derivative

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Identification

Molecular formula
C20H22N4O2
CAS Number
123456-78-9
IUPAC Name
2-amino-N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-benzamide
Molecular Weight
334.39g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2000g/cm3
Synonyms
BENZAMIDE, o-AMINO-N-ANTIPYRINYL-N-ETHYL-
Interesting facts

Exploring 2-amino-N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-benzamide

This intriguing compound, known as 2-amino-N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-benzamide, is a member of the pyrazole family and showcases several fascinating characteristics:

  • Versatile Applications: Compounds with pyrazole moieties are widely researched for their potential in pharmaceuticals, especially in the development of anti-inflammatory and analgesic drugs.
  • Structural Complexity: This compound features a branched structure combining both imine and amide functionalities, indicating its potential versatility in different chemical reactions and synthetic pathways.
  • Biological Activity: It is important to note that the presence of the benzamide and pyrazole groups may confer useful biological properties, making it a subject of interest in medicinal chemistry.
  • Research Opportunities: Scientists continue to explore the derivatives of this compound in the hopes of discovering new compounds with enhanced therapeutic properties.
  • Intriguing Synthesis: The synthesis of compounds like 2-amino-N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-benzamide often involves multi-step reactions, which can be a challenging yet rewarding process for organic chemists.

In summary, 2-amino-N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-benzamide not only stands out due to its complex structure but also holds promise for various applications in the field of medicinal chemistry. As highlighted by the saying, "complexity breeds innovation," this compound exemplifies the beauty and potential found within the realm of chemical science.

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