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Phenazone

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Identification
Molecular formula
C23H22N4O4
CAS number
60-80-0
IUPAC name
N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-4-nitro-benzamide
State
State

At room temperature, the compound is in a solid state.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.00
Boiling point (Celsius)
368.00
Boiling point (Kelvin)
641.00
General information
Molecular weight
244.28g/mol
Molar mass
244.2810g/mol
Density
1.4350g/cm3
Appearence

The compound typically presents as a solid crystalline substance.

Comment on solubility

Solubility of N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-4-nitro-benzamide

The solubility of N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-4-nitro-benzamide in various solvents can be influenced by its structural characteristics. The presence of multiple functional groups within this compound contributes to its solubility behavior:

  • Polarity: The molecule contains both polar and non-polar regions, which may lead to variable solubility in polar solvents (like water) versus non-polar solvents (like hexane).
  • Hydrogen Bonding: Functional groups, such as the amide linkage, can form hydrogen bonds, potentially enhancing solubility in polar solvents.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, suggesting that a thorough investigation at varying temperatures may yield different solubility profiles.

In summary, while N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-4-nitro-benzamide may possess limited solubility in water, it may show improved solubility in organic solvents due to its complex structure. Understanding the solubility characteristics of this compound is crucial for its applications in various chemical processes.

Interesting facts

Interesting Facts about N-(1,5-Dimethyl-3-Oxo-2-Phenyl-Pyrazol-4-Yl)-N-Ethyl-4-Nitro-Benzamide

N-(1,5-Dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-4-nitro-benzamide is a compound that showcases the fascinating interplay between nitrogen-containing heterocycles and functionalized aromatic systems. Here are some interesting aspects of this chemical:

  • Structural Complexity: The compound features both a pyrazole ring and a nitro group, creating opportunities for diverse chemical reactivity. Its intricate structure is indicative of its potential applications in medicinal chemistry.
  • Potential Biological Activity: Compounds like this one are often evaluated for their biological properties, including anti-inflammatory and antitumor activities. Researchers are exploring its efficacy in drug development, particularly within oncology.
  • Versatile Synthesis: The synthesis of N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-4-nitro-benzamide often involves multi-step processes that highlight the creativity and skill of synthetic chemists. Understanding these synthetic pathways can reveal insights into reactivity and selectivity in complex organic transformations.
  • Research Implications: This compound can serve as a model for designing new therapeutic agents, leading to further exploration in drug discovery. Its structural motifs could inspire modifications that enhance desired biological activities.
  • Interdisciplinary Connections: The chemistry of this compound bridges multiple fields, such as pharmacology, organic synthesis, and materials science, demonstrating how a single compound can influence diverse areas of research.

In summary, N-(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)-N-ethyl-4-nitro-benzamide is more than just a chemical formula; it represents a world of scientific inquiry and potential. As noted by experts in the field, "The journey from simple structures to complex molecules opens the door to revolutionary discoveries in chemistry." This compound stands as a testament to that journey.

Synonyms
BENZAMIDE, N-ANTIPYRINYL-N-ETHYL-p-NITRO-
15166-19-5
TA 7
N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-N-ethyl-4-nitrobenzamide
N-Antipyrinyl-N-ethyl-p-nitrobenzamide
BRN 0586631
N-(1,5-dimethyl-3-oxo-2-phenylpyrazol-4-yl)-N-ethyl-4-nitrobenzamide
Oprea1_866766
DTXSID10164844
SR-01000232554
SR-01000232554-1