Skip to main content

Dicyclohexylpentylbarbiturate

ADVERTISEMENT
Identification
Molecular formula
C23H36N2O3
CAS number
312-84-5
IUPAC name
1,3-dicyclohexyl-5-pentyl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, Dicyclohexylpentylbarbiturate appears as a solid due to its high melting point.

Melting point (Celsius)
191.00
Melting point (Kelvin)
464.15
Boiling point (Celsius)
387.00
Boiling point (Kelvin)
660.15
General information
Molecular weight
388.56g/mol
Molar mass
387.5560g/mol
Density
1.1138g/cm3
Appearence

Dicyclohexylpentylbarbiturate is typically a white crystalline powder. Its appearance is characterized by its fine, uniform crystal shape and clean, white color, indicative of its purity and typical of many barbiturate compounds.

Comment on solubility

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

The solubility of 1,3-dicyclohexyl-5-pentyl-hexahydropyrimidine-2,4,6-trione can be somewhat complex due to its unique chemical structure. Here are some key points to consider:

  • Polarity: This compound features a combination of cyclohexyl groups and a pentyl chain, impacting its overall polarity. Generally, non-polar compounds tend to have low solubility in polar solvents like water.
  • Solvent Compatibility: It is expected to be more soluble in non-polar organic solvents such as hexane or chloroform, which can adequately solvate its hydrophobic regions.
  • Hydrogen Bonding: The presence of functional groups capable of hydrogen bonding may allow some interaction with polar solvents, although overall solubility would still lean towards non-polar environments.
  • Temperature Dependence: As with many organic compounds, increasing temperature could enhance its solubility in various solvents; this is a common characteristic of solid compounds becoming more soluble when heated.

In summary, while 1,3-dicyclohexyl-5-pentyl-hexahydropyrimidine-2,4,6-trione is likely to be insoluble or only sparingly soluble in water, its solubility in hydrophobic solvents is expected to be significantly greater. Thus, understanding the appropriate solvent is crucial when working with this compound.

Interesting facts

1,3-Dicyclohexyl-5-pentyl-hexahydropyrimidine-2,4,6-trione

This intriguing compound belongs to the class of hexahydropyrimidines, which are of particular interest in medicinal chemistry and organic synthesis. Its unique structure features multiple cyclic systems, which confer distinctive properties and reactivity.

Key Features:

  • Structural Complexity: The presence of two cyclohexyl groups significantly enhances the compound's steric environment, providing insights into how sterics can influence chemical reactivity.
  • Potential Applications: Compounds like this are often studied for their biological activity, including potential roles in pharmaceuticals where modifications to the pyrimidine ring can lead to novel therapeutic agents.
  • Versatility: The ability to manipulate the functional groups attached to the pyrimidine core allows for the design of compounds with specific properties, making it a subject of interest for synthetic chemists.

As the saying goes, "Chemistry is the art of science," and compounds like 1,3-dicyclohexyl-5-pentyl-hexahydropyrimidine-2,4,6-trione remind us of the intricate dance of elements and bonds in the creation of new materials. Its study might lead to groundbreaking discoveries in understanding molecular interactions and their implications in biological systems.

In addition, the exploration of such compounds also showcases the importance of interdisciplinary approaches in chemistry, bridging gaps between organic synthesis, medicinal chemistry, and biological evaluation. The research surrounding these compounds not only contributes to our understanding of organic chemistry but could also pave the path for innovative drug development.

Synonyms
BRN 0764215
1,3-Dicyclohexyl-5-pentylbarbituric acid
BARBITURIC ACID, 1,3-DICYCLOHEXYL-5-PENTYL-
857-31-8
1,3-Dicyclohexyl-5-pentyl-2,4,6(1H,3H,5H)-pyrimidinetrione
DTXSID40234988
DTXCID70157479
5-24-09-00155 (beilstein handbook reference)