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Mephobarbital

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Identification
Molecular formula
C13H14N2O3
CAS number
115-38-8
IUPAC name
5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, Mephobarbital is in a solid state.

Melting point (Celsius)
181.00
Melting point (Kelvin)
454.00
Boiling point (Celsius)
398.30
Boiling point (Kelvin)
671.30
General information
Molecular weight
274.31g/mol
Molar mass
274.3140g/mol
Density
1.1580g/cm3
Appearence

Mephobarbital typically appears as a white crystalline powder.

Comment on solubility

Solubility of 5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione

The solubility of 5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione (C13H14N2O3) is an intriguing aspect of this compound. Understanding its solubility behavior is essential for applications across various fields. Here are some key points about its solubility:

  • Solvent Influence: This compound exhibits variable solubility depending on the solvent used. Common solvents such as alcohols and dimethyl sulfoxide (DMSO) can enhance its solubility.
  • Temperature Effect: Increasing the temperature typically enhances solubility. As with many organic compounds, warm solvents can dissolve more solute.
  • pH Sensitivity: The solubility can also be affected by the pH of the solution. Understanding the ionic environment can lead to better solubility characteristics.

In summary, the solubility of 5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione is influenced by the choice of solvent, temperature, and pH levels. It is clear that a comprehensive investigation can reveal the optimal conditions for achieving the highest degree of solubility, thereby enhancing its usability in practical applications.

Interesting facts

Interesting Facts about 5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione

5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione is a fascinating compound with significant implications in medicinal chemistry and drug design. Here are some noteworthy points about this intriguing molecule:

  • Structure and Function: The structure of this compound features a hexahydropyrimidine ring which contributes to its biological activity. Its unique design allows it to interact with various biological targets, making it a subject of interest for pharmaceuticals.
  • Derivatives and Similar Compounds: This compound belongs to a class of molecules known as pyrimidines. Pyrimidine derivatives often exhibit a wide range of biological activities, including antimicrobial, anti-inflammatory, and anticancer properties.
  • Research Potential: Current research is exploring the potential of 5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione as a lead compound for the development of new therapeutic agents. This compound serves as a valuable scaffold for synthesizing new derivatives that may enhance efficacy.
  • Mechanistic Studies: Scientists are investigating the mechanisms of action of this compound to understand how it interacts with biological macromolecules, such as proteins and nucleic acids. Such studies can elucidate the pathways through which this compound exerts its effects.
  • Environmental Considerations: The stability and degradation pathways of this compound are important for assessing its environmental impact. Researchers are interested in understanding how such compounds behave in various ecological contexts.

As the field of medicinal chemistry advances, the intriguing properties of compounds like 5-methyl-5-(4-phenoxyphenyl)hexahydropyrimidine-2,4,6-trione will continue to inspire researchers. The exploration of its full therapeutic potential may lead to the discovery of novel and effective treatments for various diseases.

Synonyms
5-methyl-5-(4-phenoxy-phenyl)-pyrimidine-2,4,6-trione
288102-94-3
5-methyl-5-(4-phenoxyphenyl)-1,3-diazinane-2,4,6-trione
CHEMBL176467
HQQ
5-methyl-5-(4-phenoxyphenyl)barbituric acid
CHEBI:43179
DTXSID10274336
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-methyl-5-(4-phenoxyphenyl)-
4MPM14604G
5-methyl-5-(4-phenoxyphenyl) pyrimidine-2,4,6-trione
5-methyl-5-(4-phenoxyphenyl)pyrimidine-2,4,6(1H,3H,5H)-trione
1g4k
UNII-4MPM14604G
SCHEMBL4321603
DTXCID40225816
BDBM50099118
DB03368
PD007046
NS00069143
Q27094311