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Methyprylon

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Identification
Molecular formula
C14H18N2O3
CAS number
125-97-3
IUPAC name
5-ethyl-5-phenyl-1-(1-piperidylmethyl)hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, Methyprylon is in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
72.50
Melting point (Kelvin)
345.60
Boiling point (Celsius)
390.60
Boiling point (Kelvin)
663.80
General information
Molecular weight
290.35g/mol
Molar mass
290.3520g/mol
Density
1.1450g/cm3
Appearence

Methyprylon is a crystalline powder that is typically white or off-white in color. It is relatively stable under normal conditions of storage and handling.

Comment on solubility

Solubility of 5-ethyl-5-phenyl-1-(1-piperidylmethyl)hexahydropyrimidine-2,4,6-trione

The solubility of 5-ethyl-5-phenyl-1-(1-piperidylmethyl)hexahydropyrimidine-2,4,6-trione is influenced by several factors due to its complex structure. This compound, which contains both hydrophobic and hydrophilic groups, tends to exhibit varying solubility characteristics in different solvents.

Key points regarding its solubility include:

  • Polar solvents: The presence of the piperidyl group may enhance solubility in polar solvents like water and methanol.
  • Nonpolar solvents: However, the extensive hydrophobic regions, particularly from the ethyl and phenyl substituents, can limit solubility in nonpolar solvents such as hexane or benzene.
  • Temperature dependence: The solubility might increase with temperature, as is common with many organic compounds, but this requires empirical validation.

In summary, the solubility of this compound can be described as moderate to variable, particularly depending on the solvent environment. Understanding these solubility trends is crucial for applications in pharmaceuticals and materials science, where the bioavailability of compounds can be heavily influenced by their solubility characteristics.

Interesting facts

Interesting Facts about 5-Ethyl-5-phenyl-1-(1-piperidylmethyl)hexahydropyrimidine-2,4,6-trione

This fascinating compound is a member of the pyrimidine family, which is characterized by a six-membered ring containing two nitrogen atoms. Its structure gives rise to numerous interesting chemical and biological properties that make it a subject of study in various fields.

Key Features

  • Molecular Complexity: The presence of multiple functional groups and a piperidine moiety adds layers of complexity to its reactivity and interactions.
  • Pharmaceutical Potential: Compounds like this one can serve as starting points for drug development, particularly in medicinal chemistry owing to their ability to interact with biological systems.
  • Diverse Applications: The structure hints at potential applications in neuropharmacology, perhaps acting on neurotransmitter systems due to the presence of the piperidine group.

Moreover, the specific arrangement of ethyl and phenyl groups in its structure may also influence its binding affinity and selectivity toward various biological targets. This could lead to exciting discoveries in the realm of new therapies or synthetic routes to complex molecules.

As chemists delve into the exploration of such compounds, the alignment of theoretical predictions with practical outcomes is crucial. As J.D. Watson once said, "Science is a way of thinking much more than it is a body of knowledge," highlighting the importance of both understanding and experimentation in the field of chemistry.

Conclusion

With its intriguing characteristics and possible applications, 5-ethyl-5-phenyl-1-(1-piperidylmethyl)hexahydropyrimidine-2,4,6-trione continues to be a compound worthy of exploration. Its contribution to the fields of chemistry and pharmacology could lead to innovations in therapeutic agents, making it a valuable subject of ongoing research.

Synonyms
5-ethyl-5-phenyl-1-(piperidin-1-ylmethyl)pyrimidine-2,4,6(1H,3H,5H)-trione
Oprea1_612690
STK040800
AKOS005383489
SR-01000232577
SR-01000232577-1