Allyl Barbituric Acid

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Identification

Molecular formula
C11H16N2O4
CAS Number
131-29-5
IUPAC Name
5-allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione
Molecular Weight
224.25g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2600g/cm3
Synonyms
5-Allyl-1-(4-hydroxycyclohexyl)barbituric acid
Interesting facts

Interesting Facts About 5-Allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione

5-Allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione is a fascinating compound notable for its unique structural features and potential applications. Here are some remarkable facts about this compound:

  • Diverse Functionality: This compound belongs to the pyrimidine family, which is characterized by a six-membered ring containing nitrogen atoms. The incorporation of an allyl group enhances its reactivity and opens doors to various chemical reactions.
  • Hydroxy Group Impact: The presence of a hydroxy group on the cyclohexyl ring contributes to the compound's stability and polarity, making it a potential candidate for biological activities.
  • Biological Relevance: Compounds similar to this have been studied for their therapeutic effects. Their ability to interact with biological systems positions them as candidates for pharmaceutical development.
  • Potential in Organic Synthesis: The unique structural attributes of this compound provide opportunities for innovative synthetic pathways, particularly in the creation of complex organic molecules.

An exciting quote in the field of chemistry states, "Chemistry is the central science; it connects physics with other natural sciences such as geology and biology." This compound exemplifies that connection, bridging synthetic chemistry with potential biological applications.

As research advances, compounds like 5-allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione may unveil new horizons in both materials science and medicinal chemistry, underscoring the ever-evolving landscape of chemical discovery.

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