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Diallyl Ethylphenylmalonate

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Identification
Molecular formula
C16H20N2O3
CAS number
67957-65-3
IUPAC name
1,3-diallyl-5-ethyl-5-phenyl-hexahydropyrimidine-2,4,6-trione
State
State

The compound is typically in a liquid state at room temperature.

Melting point (Celsius)
18.00
Melting point (Kelvin)
291.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
304.38g/mol
Molar mass
304.3820g/mol
Density
1.1721g/cm3
Appearence

The compound is usually found as a colorless to pale yellow liquid, characterized by a distinct aromatic odor.

Comment on solubility

Solubility of 1,3-Diallyl-5-ethyl-5-phenyl-hexahydropyrimidine-2,4,6-trione

The solubility of 1,3-diallyl-5-ethyl-5-phenyl-hexahydropyrimidine-2,4,6-trione can be understood through the evaluation of its molecular structure and interactions with solvents. This compound features a complex arrangement of functional groups that affect its solubility in various media.

Here are some points to consider when assessing its solubility:

  • Polar vs. Non-Polar Solvents: Due to the presence of multiple functional groups, the compound may exhibit different solubility profiles in polar and non-polar solvents. In general, compounds that are polar tend to dissolve well in polar solvents like water or alcohols.
  • Hydrogen Bonding: The ability to form hydrogen bonds can significantly enhance solubility in polar solvents. If this compound can engage in hydrogen bonding, it is likely to be more soluble in water.
  • Hydrophobic Interactions: Conversely, the presence of phenyl groups may introduce hydrophobic characteristics, which could limit its solubility in highly polar solvents.
  • Temperature Dependence: The solubility can also change with temperature; some compounds become more soluble as the temperature increases, while others may not.

In summary, the solubility of 1,3-diallyl-5-ethyl-5-phenyl-hexahydropyrimidine-2,4,6-trione may vary significantly based on the solvent used and environmental conditions. Determining the specific solubility characteristics requires experimental data, and further investigations are essential to fully understand its behavior in different solvents.

Interesting facts

Interesting Facts about 1,3-Diallyl-5-ethyl-5-phenyl-hexahydropyrimidine-2,4,6-trione

1,3-Diallyl-5-ethyl-5-phenyl-hexahydropyrimidine-2,4,6-trione is a fascinating compound that captures the interest of chemists due to its unique structure and potential applications. This organic compound is part of the pyrimidine family, known for its six-membered ring that contains two nitrogen atoms. Below are some intriguing aspects of this compound:

  • Structural Complexity: The presence of both diallyl and phenyl groups contributes to its structural diversity, allowing for a range of possible chemical reactions and interactions.
  • Bioactivity Potential: Compounds of this type have been studied for their biological properties, particularly in medicinal chemistry. Their ability to interact with biological systems makes them potential candidates for drug development.
  • Versatility: The functional groups attached to this structure enable it to participate in various chemical reactions, including nucleophilic substitutions and additions, making it a versatile molecule in organic synthesis.
  • Research Applications: Its unique reactivity profiles have spurred interest in academic research, leading to investigations into its potential uses in creating advanced materials or pharmaceuticals.

As quoted by leading researchers in organic chemistry, "The beauty of molecules like 1,3-diallyl-5-ethyl-5-phenyl-hexahydropyrimidine-2,4,6-trione lies in their ability to connect curiosity with real-world applications."
This compound exemplifies the bridge between basic chemical research and the quest for innovative solutions in health and material science.

Through ongoing studies, scientists continue to unveil the secrets of this intriguing compound, underscoring the importance of chemical research in understanding and harnessing the properties of complex organic molecules.

Synonyms
1,3-Diallyl-5-ethyl-5-phenylbarbituric acid
16846-63-2
5-ethyl-5-phenyl-1,3-bis(prop-2-enyl)-1,3-diazinane-2,4,6-trione
N,N'-Diallylphenobarbital
BRN 0306817
BARBITURIC ACID, 1,3-DIALLYL-5-ETHYL-5-PHENYL-
DTXSID90937497
1,3-Diallyl-5-ethyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione
5-Ethyl-5-phenyl-1,3-di(prop-2-en-1-yl)-1,3-diazinane-2,4,6-trione