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Fenazone

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Identification
Molecular formula
C20H22N3O
CAS number
2009-15-8
IUPAC name
5-benzyl-2-(1-methyl-4-piperidyl)-4-phenyl-1H-pyrazol-3-one
State
State

At room temperature, Fenazone is in a solid state. It appears as a crystalline substance.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
458.00
Boiling point (Kelvin)
731.15
General information
Molecular weight
316.42g/mol
Molar mass
316.4180g/mol
Density
1.2000g/cm3
Appearence

Fenazone appears as a white crystalline powder. The powder is typically very fine and may have a slight white or off-white color. It is often used in its pure form for analytical purposes or in pharmaceuticals.

Comment on solubility

Solubility of 5-benzyl-2-(1-methyl-4-piperidyl)-4-phenyl-1H-pyrazol-3-one

The solubility of 5-benzyl-2-(1-methyl-4-piperidyl)-4-phenyl-1H-pyrazol-3-one is influenced by several factors, making it a fascinating compound to study.

Key Points on Solubility:

  • Polar vs. Non-Polar: The compound contains both polar and non-polar segments, which may result in varied solubility in different solvents.
  • Protic vs. Aprotic Solvents: Its ability to dissolve in protic solvents (like water) may be limited, while it could show better solubility in aprotic solvents (such as DMSO or acetone).
  • Temperature Influence: Increased temperature typically enhances solubility for many organic compounds, and this one may behave similarly.

“Solubility is not just a simple ratio; it's a dynamic interplay of molecular interactions.”

Understanding the solubility of this compound is essential for its applications in medicinal chemistry, where the bioavailability and distribution of a drug can significantly impact its efficacy.

Interesting facts

Exploring 5-benzyl-2-(1-methyl-4-piperidyl)-4-phenyl-1H-pyrazol-3-one

5-benzyl-2-(1-methyl-4-piperidyl)-4-phenyl-1H-pyrazol-3-one is a compound that belongs to the class of pyrazolone derivatives. This intriguing compound has drawn attention for its potential applications in various fields such as medicinal chemistry and pharmacology.

Key Characteristics

  • Structural Complexity: The structure of this compound features a pyrazolone core, which is a five-membered heterocyclic ring that contains nitrogen atoms. This ring is fused with multiple aromatic groups, providing a unique characteristic that can influence its biological activity.
  • Biological Activity: Research has indicated that compounds in the pyrazolone class may exhibit anti-inflammatory, analgesic, and antipyretic properties. As scientists delve deeper, they aim to uncover more about how this specific compound interacts with biological systems.
  • Pharmacophore Potential: The piperidine substituent attached to the pyrazolone structure opens up possibilities for engaging with various biological targets, making it an interesting lead for drug design.

Future Research Directions

With the ongoing exploration of 5-benzyl-2-(1-methyl-4-piperidyl)-4-phenyl-1H-pyrazol-3-one, there are several avenues that researchers might pursue:

  1. Investigating its mechanism of action in biological systems.
  2. Conducting structure-activity relationship studies to optimize its efficacy and selectivity.
  3. Exploring its potential as a therapeutic agent in treating various diseases such as pain, inflammation, or even neurodegenerative disorders.

Conclusion

In summary, 5-benzyl-2-(1-methyl-4-piperidyl)-4-phenyl-1H-pyrazol-3-one is a fascinating compound that bridges the gap between organic synthesis and pharmacology. Its complex structure, coupled with its potential biological activity, makes it an exciting subject for further investigation. As researchers continue to unlock its secrets, the compound may pave the way for new therapeutic agents in the future.

Synonyms
3-Pyrazolin-5-one, 3-benzyl-1-(1-methyl-4-piperidyl)-4-phenyl-
7460-01-7
DTXSID90225568
3-Benzyl-1-(1-methyl-4-piperidyl)-4-phenyl-3-pyrazolin-5-one
1,2-Dihydro-2-(1-methyl-4-piperidinyl)-4-phenyl-5-(phenylmethyl)-3H-pyrazol-3-one
3H-Pyrazol-3-one, 1,2-dihydro-2-(1-methyl-4-piperidinyl)-4-phenyl-5-(phenylmethyl)-