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Allylcyclopentenohexahydropyrimidinetrione

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Identification
Molecular formula
C15H21N3O3
CAS number
21351-29-9
IUPAC name
5-allyl-5-cyclopent-2-en-1-yl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, this compound is in a solid state. It is typically handled as a powder or as small crystalline pieces.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.20
Boiling point (Celsius)
267.50
Boiling point (Kelvin)
540.70
General information
Molecular weight
265.32g/mol
Molar mass
265.3210g/mol
Density
1.2500g/cm3
Appearence

The compound is a crystalline solid with a white to off-white appearance. Its texture can range from fine powder to slightly granular.

Comment on solubility

Solubility of 5-allyl-5-cyclopent-2-en-1-yl-hexahydropyrimidine-2,4,6-trione

The solubility characteristics of 5-allyl-5-cyclopent-2-en-1-yl-hexahydropyrimidine-2,4,6-trione are influenced by its unique structural features. This chemical compound exhibits interesting solubility behavior which can be summarized as follows:

  • Polarity: The presence of functional groups significantly affects its polarity, which in turn influences solubility in various solvents.
  • Solvent Compatibility: It is typically more soluble in polar organic solvents such as dimethyl sulfoxide (DMSO) and methanol compared to non-polar solvents.
  • Hydrogen Bonding: The ability to engage in hydrogen bonding enhances solubility in water to some extent, although it may not be highly soluble.
  • Temperature Dependent: Like many compounds, solubility can also be temperature-dependent, with increased temperatures generally leading to higher solubility.

In summary, while 5-allyl-5-cyclopent-2-en-1-yl-hexahydropyrimidine-2,4,6-trione may not be universally soluble, it demonstrates a degree of solubility in specific solvents due to its structural properties. Exploring these solubility patterns can provide valuable insights into its potential applications in various fields.

Interesting facts

Interesting Facts about 5-allyl-5-cyclopent-2-en-1-yl-hexahydropyrimidine-2,4,6-trione

This fascinating compound, a derivative of hexahydropyrimidine, combines the intriguing structural features of both alkenes and cyclic imides. Its unique name hints at a complex molecular structure that brings together various functional groups, which certainly piques the interest of chemists.

Key Characteristics

  • Diverse Functional Groups: The presence of multiple functional groups allows this compound to participate in a variety of reactions, making it a potential candidate for further synthetic applications.
  • Synthetic Utility: This compound may serve as a versatile intermediate in the synthesis of more complex organic molecules, particularly in medicinal chemistry where modifications can lead to new pharmaceutical agents.
  • Structural Insights: The cyclopentene ring introduces intrinsic strain, which often results in enhanced reactivity, a compelling aspect for chemists exploring efficient reaction pathways.
  • Potential Biological Activity: Compounds with similar structural features are often explored for their biological properties, which might suggest pharmacological potential.

Furthermore, the structural complexity of 5-allyl-5-cyclopent-2-en-1-yl-hexahydropyrimidine-2,4,6-trione encourages investigations into its stereochemistry, providing a rich avenue for research. As we continue to explore the myriad applications of organic compounds, this unique structure promises to contribute to various fields, especially in the pursuit of new drugs and materials.

In the words of renowned chemist Linus Pauling: "The nature of the chemical bond is the most important subject in all of chemistry." Indeed, the intriguing nature of this compound exemplifies the beauty and complexity of chemical bonds and structures.

Synonyms
Cyclopentobarbital
Allylpental
Cyclopental
Ciclopal
Cyclopal
Cyclopen
Dormisan
Allylcyclopentenylbarbital
76-68-6
Cyclopentenyl allylbarbituric acid
5-Allyl-5-(2-cyclopenten-1-yl)barbituric acid
5-Allyl-5-(2-cyclopentenyl)barbituric acid
EINECS 200-979-6
BRN 0234280
cyclopentenylallylbarbituric acid
2230XWG55Q
BARBITURIC ACID, 5-ALLYL-5-(2-CYCLOPENTENYL)-
5-cyclopent-2-en-1-yl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione
CYCLOPENTOBARBITAL [MI]
5-24-09-00269 (Beilstein Handbook Reference)
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(2-cyclopenten-1-yl)-5-(2-propenyl)-
5-(2-Cyclopenten-1-yl)-5-(2-propenyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
Cyclopentobarbitone
Cyclopentobarbital (1.0mg/ml in Acetonitrile)
UNII-2230XWG55Q
SCHEMBL713311
DTXSID90871549
CHEBI:134951
NS00041057
Q5198932
5-(Cyclopent-2-en-1-yl)-5-(prop-2-en-1-yl)-1,3-diazinane-2,4,6-trione
5-Allyl-5-(2-cyclopenten-1-yl)-2,4,6(1H,3H,5H)-pyrimidinetrione #
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(2-cyclopenten-1-yl)-5-(2-propen-1-yl)-
200-979-6