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Cyclolegnoide lactone

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Identification
Molecular formula
C13H20N2O3
CAS number
23450-52-4
IUPAC name
5-allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, the compound exists as a solid. It's generally stable and unreactive in moisture and air, maintaining its form unless conditions are significantly altered.

Melting point (Celsius)
188.30
Melting point (Kelvin)
461.45
Boiling point (Celsius)
426.70
Boiling point (Kelvin)
699.85
General information
Molecular weight
237.31g/mol
Molar mass
237.3080g/mol
Density
1.2105g/cm3
Appearence

5-Allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione appears as a solid with a crystalline structure. It usually features a white or off-white color, and is characterized by a smooth texture. This compound is known for its stability in ambient conditions and typically retains its structure unless exposed to reactive chemicals.

Comment on solubility

Solubility of 5-allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione

The solubility of 5-allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione can be influenced by several factors, including its chemical structure and interactions with solvents. Here are some key points to consider:

  • Polar and Non-Polar Character: This compound contains multiple functional groups that may affect its polarity. High polarity could increase solubility in polar solvents such as water, while a more non-polar characteristic would favor solubility in organic solvents like hexane.
  • Hydrophilicity vs Hydrophobicity: The balance between hydrophilic (water-attracting) and hydrophobic (water-repelling) portions of the molecule plays a crucial role. As a general rule, compounds that contain more polar functional groups tend to be more soluble in water.
  • Temperature Effects: Solubility can vary with temperature. Typically, increased temperatures enhance solubility due to enhanced molecular motion.
  • Interactions with Solvents: The presence of specific solvation effects, like hydrogen bonding or Van der Waals forces with a solvent, can dramatically alter solubility. This can make certain solvents more effective than others for dissolution.

In conclusion, while concrete data on the solubility of 5-allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione in various solvents may not be readily available, understanding the factors that govern solubility can guide predictions about its behavior. As the saying goes, "Like dissolves like," so considering the compound's characteristics relative to potential solvents will provide insights into its solubility profile.

Interesting facts

Interesting Facts about 5-Allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione

This unique compound is noteworthy for its intriguing structure and potential applications in various fields of chemistry. As a pyrimidine derivative, it features a pyrimidine ring fused with cyclohexyl and allyl substituents, yielding significant potential for reactivity and applications. Below are some key highlights:

  • Bioactivity: Compounds like this one are often studied for their biological properties and possible pharmacological effects. Pyrimidine derivatives are known to exhibit a range of biological activities, including *antiviral*, *antitumor*, and *antimicrobial* properties.
  • Building Block: The presence of multiple reactive functional groups in 5-allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione makes it a versatile *building block* in organic synthesis. Chemists often use such compounds in the creation of more complex molecules.
  • Reactivity: The trione functional groups impart interesting reactivity. They can undergo various transformations, which opens avenues for *synthetic pathways* leading to new materials or drugs.
  • Research Interest: This compound and its derivatives are subjects of ongoing research due to their potential applications in drug design and development. The unique blend of the *cyclic* structure and the allyl group may contribute to novel interactions with biological targets.
  • Functionalization Possibilities: The reactivity of the allyl moiety can be exploited to create derivatives with diverse functionalities, further expanding its utility in organic synthesis.

In conclusion, 5-allyl-1-cyclohexyl-hexahydropyrimidine-2,4,6-trione serves as a fascinating example of a complex organic compound with potential across several scientific domains. As research continues to unveil its properties, it may lead to innovative applications in medicinal chemistry and materials science.

Synonyms
890-05-1
5-Allyl-1-cyclohexylbarbituric acid
BRN 0752916
BARBITURIC ACID, 5-ALLYL-1-CYCLOHEXYL-
1-cyclohexyl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione
5-Allyl-1-cyclohexyl-2,4,6(1H,3H,5H)-pyrimidinetrione
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-allyl-1-cyclohexyl-
SCHEMBL10824623
DTXSID301008593
3-Cyclohexyl-6-hydroxy-5-(prop-2-en-1-yl)pyrimidine-2,4(3H,5H)-dione