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Allylbarbituric acid

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Identification
Molecular formula
C10H14N2O3
CAS number
77-26-9
IUPAC name
5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, Allylbarbituric acid is found in a solid state. It has a crystalline structure, and depending on its processing, it can be a fine to a coarse powder.

Melting point (Celsius)
66.00
Melting point (Kelvin)
339.15
Boiling point (Celsius)
322.00
Boiling point (Kelvin)
595.15
General information
Molecular weight
225.23g/mol
Molar mass
225.2600g/mol
Density
1.1700g/cm3
Appearence

Allylbarbituric acid typically appears as a white to off-white crystalline powder. Its solid form often displays a dull sheen or matte finish. This compound is often formulated into tablets or capsules for its applications, where its appearance may vary with additives.

Comment on solubility

Solubility of 5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione

The solubility of 5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione can be quite intriguing due to its structural characteristics. Understanding its solubility behavior involves several factors:

  • Polar vs Non-Polar: The compound possesses amino and carbonyl groups, which may enhance its polarity, potentially increasing solubility in polar solvents like water.
  • Functional Groups: The presence of the amino group specifically can lead to hydrogen bonding, further aiding solubility in aqueous environments.
  • Solvent Compatibility: It is likely to be more soluble in more polar aprotic solvents, such as methanol or dimethyl sulfoxide, than in nonpolar solvents.

It is important to note that the specific solubility may also depend on factors such as:

  • Temperature: Typically, an increase in temperature may enhance solubility.
  • pH of the solution: Changes in pH can alter the ionization state of the amino group, which may affect solubility significantly.

In conclusion, the solubility of 5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione is likely high in polar solvents but may require empirical testing for precise quantification. As with many compounds, “the key to understanding solubility lies in the balance of molecular interactions.”

Interesting facts

Interesting Facts about 5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione

5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione is a fascinating compound in the realm of organic chemistry, particularly notable for its structural configuration and potential applications. Here are some engaging insights about this compound:

  • Versatile Structure: The unique hexahydropyrimidine ring system gives rise to various possible isomers and derivatives. This versatility enables chemists to explore modifications that can lead to compounds with tailored properties.
  • Biological Significance: Compounds with similar structures are often investigated for their biological activity. The presence of the aminopropyl group hints at potential interactions within biological systems, possibly influencing enzyme activity or receptor binding.
  • Synthetic Pathways: The synthesis of this compound can involve several intriguing chemical reactions, including cyclization and substitution reactions. Understanding these pathways is essential for developing efficient synthetic strategies in organic chemistry.
  • Potential Applications: Due to its structural characteristics, 5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione might find its place in medicinal chemistry, particularly in the development of pharmaceuticals that target specific biological pathways.
  • Research Interests: Ongoing studies on compounds of this nature contribute to the broader knowledge base in fields such as drug development, agrochemicals, and synthetic material science.

Emphasizing the importance of structure-function relationships in chemical compounds, it’s intriguing to consider how a small change in molecular architecture can lead to significant differences in activity or application. As the renowned chemist Linus Pauling once said, "The nature of the chemical bond is a great subject of science that has implications far beyond the realm of chemistry." Understanding compounds like 5-allyl-5-(2-aminopropyl)hexahydropyrimidine-2,4,6-trione paves the way for innovative discoveries and advancements in various scientific fields.

Synonyms
14321-29-0
BARBITURIC ACID, 5-ALLYL-5-(2-AMINOPROPYL)-
Kwasu 5-allilo-5-(beta-aminopropylo)-barbiturowego [Polish]
Kwasu 5-allilo-5-(beta-aminopropylo)-barbiturowego
DTXSID60931780
5-(2-Aminopropyl)-4,6-dihydroxy-5-(prop-2-en-1-yl)pyrimidin-2(5H)-one