Interesting facts
Interesting Facts about 5-Allyl-1-phenyl-hexahydropyrimidine-2,4,6-trione
5-Allyl-1-phenyl-hexahydropyrimidine-2,4,6-trione is a fascinating compound in the realm of organic chemistry, known for its unique structure and potential applications. Below are some engaging insights into this intriguing molecule:
- Structure Diversity: The unique combination of a hexahydropyrimidine ring system with a phenyl group and an allyl substituent contributes to its structural diversity, making it a subject of interest for synthetic chemists.
- Reactivity: The presence of the trione functional groups makes this compound highly reactive. This reactivity can lead to interesting synthetic pathways, which can be used to create more complex molecules.
- Potential Applications: Compounds like 5-Allyl-1-phenyl-hexahydropyrimidine-2,4,6-trione may find applications in pharmaceuticals due to their biological activity and ability to act as intermediates in drug synthesis.
- Natural Product Inspiration: Chemical structures similar to this compound are often inspired by natural products, which can influence biochemical pathways. Exploring such compounds can lead to discoveries in drug design.
- Research Opportunities: This compound presents numerous opportunities for research, especially in:
- Medicinal Chemistry
- Organic Synthesis
- Bioorganic chemistry
To quote a renowned chemist, "Chemistry is not just about reactions; it’s about understanding the subtleties of structure and function." Investigating compounds like 5-Allyl-1-phenyl-hexahydropyrimidine-2,4,6-trione brings us one step closer to unlocking the potential of organic chemistry!
Synonyms
786-56-1
5-Allyl-1-phenylbarbituric acid
BRN 0751165
1-phenyl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione
BARBITURIC ACID, 5-ALLYL-1-PHENYL-
5-Allyl-1-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-allyl-1-phenyl-
SCHEMBL2364824
DTXSID20999881
6-Hydroxy-3-phenyl-5-(prop-2-en-1-yl)pyrimidine-2,4(3H,5H)-dione
Solubility of 5-allyl-1-phenyl-hexahydropyrimidine-2,4,6-trione
The solubility of the compound 5-allyl-1-phenyl-hexahydropyrimidine-2,4,6-trione can present both intriguing possibilities and challenging aspects. Generally, this compound exhibits limited solubility in water, which can be attributed to its larger molecular structure and the presence of hydrophobic regions. However, its solubility may improve in certain organic solvents.
Factors Influencing Solubility:
It is essential to consider that solubility can vary widely depending on the specific solvent used. As a rule of thumb:
In summary, while 5-allyl-1-phenyl-hexahydropyrimidine-2,4,6-trione exhibits limited solubility in aqueous environments, it may release its potential in organic media. Understanding these solubility behaviors is crucial for applications in chemical synthesis and analysis.