Skip to main content

Dodecahydropyrimidine

ADVERTISEMENT
Identification
Molecular formula
C14H23N1O3
CAS number
1197-55-3
IUPAC name
1-allyl-5-(cyclohexen-1-yl)-3,5-dimethyl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, the compound exists in a solid state. It is stable under standard conditions and does not readily evaporate or sublimate.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
406.00
Boiling point (Kelvin)
679.15
General information
Molecular weight
251.37g/mol
Molar mass
251.3720g/mol
Density
1.1501g/cm3
Appearence

The compound appears as a crystalline solid with a white to off-white color. The crystals are typically fine and powdery, with a smooth texture.

Comment on solubility

Solubility of 1-allyl-5-(cyclohexen-1-yl)-3,5-dimethyl-hexahydropyrimidine-2,4,6-trione

The solubility of the compound 1-allyl-5-(cyclohexen-1-yl)-3,5-dimethyl-hexahydropyrimidine-2,4,6-trione can be influenced by various factors, including its molecular structure and the presence of different functional groups. In general, the solubility behaviors of organic compounds can vary significantly depending on the following:

  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents like water, while non-polar groups often favor solubility in organic solvents.
  • Hydrogen Bonding: Compounds that can participate in hydrogen bonding typically exhibit higher solubility in polar solvents. The intricate structure of this compound may allow for potential hydrogen bonding with suitable solvents.
  • Size and Mass: Larger and more complex molecules may experience decreased solubility due to steric hindrance and increased molecular weight. The bulky nature of the cyclohexenyl group in this compound might affect its solubility profile.
  • Temperature: Solubility is often temperature-dependent; increasing temperature can lead to increased solubility for many substances.

In summary, the solubility of 1-allyl-5-(cyclohexen-1-yl)-3,5-dimethyl-hexahydropyrimidine-2,4,6-trione is likely to be influenced by its unique structural characteristics and may require careful consideration of the solvent characteristics and conditions for optimal dissolution.

Interesting facts

Interesting Facts about 1-allyl-5-(cyclohexen-1-yl)-3,5-dimethyl-hexahydropyrimidine-2,4,6-trione

This fascinating compound belongs to the class of pyrimidine derivatives, which are known for their diverse biological activities. Here are some engaging insights:

  • Versatile Applications: Compounds containing the pyrimidine ring structure are widely studied for their roles in pharmaceuticals, including as antiviral, antibacterial, and anticancer agents.
  • Natural Inspiration: The structural components of 1-allyl-5-(cyclohexen-1-yl)-3,5-dimethyl-hexahydropyrimidine-2,4,6-trione resonate with natural products, highlighting the treasure trove of inspiration that nature provides for synthetic chemistry.
  • Structure-Activity Relationship: The intricate arrangement of functional groups in this compound may lead to a variety of biological activities, necessitating in-depth studies to understand how modifications impact its efficacy.
  • Complex Synthesis: The creation of this compound likely involves multiple synthetic steps, reflecting the challenges and intricacies of organic synthesis.
  • Mechanistic Insights: Studying such compounds offers insights into reaction mechanisms and can elucidate the principles of reactivity in organic chemistry, making it an important topic for students and researchers.

As a reminder of the compound's significance, one may consider the quote: "Chemistry is the study of transformation, and compounds like these are the embodiment of transformation in nature."

Overall, 1-allyl-5-(cyclohexen-1-yl)-3,5-dimethyl-hexahydropyrimidine-2,4,6-trione not only expands our understanding of pyrimidine chemistry but also reinforces the essential role of synthetic compounds in advancing medicinal science.

Synonyms
14357-94-9
3-Allyl-5-(1-cyclohexen-1-yl)-1,5-dimethylbarbituric acid
N-Allylhexobarbital
5-(cyclohexen-1-yl)-1,5-dimethyl-3-prop-2-enyl-1,3-diazinane-2,4,6-trione
N-Allylmethylhexabital
BRN 0276994
BARBITURIC ACID, 3-ALLYL-5-(1-CYCLOHEXEN-1-YL)-1,5-DIMETHYL-
5-24-09-00256 (Beilstein Handbook Reference)
DTXSID30931954
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-cyclohexen-1-yl)-3,5-dimethyl-1-(2-propenyl)-
5-(CYCLOHEX-1-EN-1-YL)-1,5-DIMETHYL-3-(PROP-2-EN-1-YL)-1,3-DIAZINANE-2,4,6-TRIONE