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Cycloate

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Identification
Molecular formula
C13H24N2O3
CAS number
1134-23-2
IUPAC name
1,3-dicyclohexyl-5-ethyl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, cycloate is typically a solid and can exist in a crystalline form under standard conditions.

Melting point (Celsius)
31.50
Melting point (Kelvin)
304.65
Boiling point (Celsius)
242.00
Boiling point (Kelvin)
515.15
General information
Molecular weight
340.49g/mol
Molar mass
339.4820g/mol
Density
1.0990g/cm3
Appearence

Cycloate appears as a white crystalline solid. It may also have forms that are pale-yellow depending on its purity and conditions of crystallization.

Comment on solubility

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

The solubility of 1,3-dicyclohexyl-5-ethyl-hexahydropyrimidine-2,4,6-trione can vary significantly depending on the solvent used and the temperature conditions. This compound features multiple functional groups that can influence its interaction with solvents. Here are some key points regarding its solubility:

  • Polar solvents: The presence of nitrogen and carbonyl groups in the structure may allow for some degree of solubility in polar solvents such as methanol or ethanol.
  • Nonpolar solvents: Due to the bulky cyclohexyl groups, this compound is likely to exhibit better solubility in nonpolar solvents such as hexane or toluene.
  • Temperature influence: Like many organic compounds, solubility can increase with temperature, so heating the solvent may enhance the dissolution process.
  • Hydrophobicity: The high hydrophobic character from the cyclohexyl rings may limit its overall solubility in water, making it more favorable to organic solvents.

In conclusion, while 1,3-dicyclohexyl-5-ethyl-hexahydropyrimidine-2,4,6-trione might exhibit limited solubility in water, it can achieve reasonable solubility in appropriately chosen organic solvents, making it versatile for various chemical applications.

Interesting facts

Interesting Facts about 1,3-Dicyclohexyl-5-ethyl-Hexahydropyrimidine-2,4,6-trione

This fascinating compound, 1,3-dicyclohexyl-5-ethyl-hexahydropyrimidine-2,4,6-trione, belongs to a class of chemicals known for their unique structural properties and potential applications in various fields. Below are some interesting aspects to consider:

  • Diverse Applications: Due to its structural characteristics, this compound may find uses in pharmaceuticals, agrochemicals, and materials science. The pyrimidine ring often serves as a key structure in drug discovery.
  • Structure-Activity Relationship (SAR): Compounds with similar polycyclic structures have demonstrated significant biological activity, making SAR studies vital for understanding how modifications to the compound's structure affect its function.
  • Catalytic Properties: Compounds containing trione functional groups often exhibit interesting catalytic properties in organic synthesis. Exploring the reactivity of this compound could lead to new synthetic pathways.
  • Cyclic Chemistry: The cyclic nature of the cyclohexyl groups introduces steric effects that can influence the compound's reactivity and interaction with other molecules. This opens avenues for studying molecular recognition and binding.

In the words of chemist Robert H. Grubbs, "Advances in chemistry often come from the unexpected interactions of seemingly simple compounds."
As we delve deeper into the study of 1,3-dicyclohexyl-5-ethyl-hexahydropyrimidine-2,4,6-trione, we may unearth valuable insights that extend beyond the compound itself.

With continued research, compounds like this one stand to contribute significantly to the development of innovative solutions in science, making them a captivating subject for chemists and researchers alike.

Synonyms
BRN 0694287
1,3-Dicyclohexyl-5-ethylbarbituric acid
BARBITURIC ACID, 1,3-DICYCLOHEXYL-5-ETHYL-
851-35-4
1,3-Dicyclohexyl-5-ethyl-2,4,6(1H,3H,5H)-pyrimidinetrione
2,4,6(1H,3H,5H)-Pyrimidinetrione, 1,3-dicyclohexyl-5-ethyl-
5-24-09-00122 (Beilstein Handbook Reference)
DTXSID80234220
DTXCID80156711