Interesting facts
Interesting Facts About 5-Ethyl-5-hexyl-hexahydropyrimidine-2,4,6-trione
The compound 5-ethyl-5-hexyl-hexahydropyrimidine-2,4,6-trione is a fascinating example of a pyrimidine derivative, known for its complex structure and potential applications in various fields. Here are some intriguing aspects about this compound:
- Structural Composition: This compound belongs to the class of hexahydropyrimidines, which are heterocyclic compounds containing nitrogen atoms in the ring structure. The presence of ethyl and hexyl groups contributes to its diverse chemical properties.
- Biological Significance: Pyrimidine derivatives play crucial roles in biology, particularly in the synthesis of nucleic acids, such as DNA and RNA. This connection to genetic material makes compounds like this one of keen interest in biochemical research.
- Potential Applications: Compounds similar to 5-ethyl-5-hexyl-hexahydropyrimidine-2,4,6-trione are being explored for their potential as pharmaceuticals, particularly in the development of anti-cancer and anti-viral agents. Their varied substituents can influence biological activity.
- Reactivity and Chemistry: The positions of the keto groups (carbonyls) at the 2, 4, and 6 positions can significantly affect the reactivity of this compound. Understanding the mechanisms behind its reactivity can lead to new synthetic pathways for creating vinyl-based polymers and other useful materials.
- Synthesis: The synthesis of hexahydropyrimidine-2,4,6-triones is typically achieved through a variety of methods, including cyclization reactions. This highlights the versatility of organic synthesis techniques in producing complex compounds with specific functional groups.
As a chemistry student or scientist, exploring compounds like 5-ethyl-5-hexyl-hexahydropyrimidine-2,4,6-trione can immensely broaden your understanding of organic chemistry and its applications in real-world scenarios. The intricate balance between structure and function in such compounds exemplifies the beauty of chemistry.
Synonyms
Ortal
HEXETHAL
77-30-5
5-Ethyl-5-hexylbarbituric acid
Barbituric acid, 5-ethyl-5-hexyl-
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-hexyl-
Acide hexylethylbarbiturique
NSC 32303
62AYA1LUDJ
5-Ethyl-5-hexyl-2,4,6(1H,3H,5H)-pyrimidinetrione
NSC-32303
Hexethal (VAN)
Ortol (VAN)
UNII-62AYA1LUDJ
Acide hexylethylbarbiturique [French]
5-ethyl-5-hexyl-1,3-diazinane-2,4,6-trione
Athyl-n-hexylbarbitursaure
SCHEMBL712742
2,4,6(1H,3H,5H)-Pyrimidinetrione,5-ethyl-5-hexyl-
CHEMBL1797004
DTXSID20871618
DTXSID30227809
PSTVHRSUNBSVIJ-UHFFFAOYSA-N
WLN: T6VMVMV FHJ F6 F2
EX-A5403
NSC32303
Barbituric acid, 5-ethyl-5-n-hexyl-
5-HEXYL-5-ETHYLBARBITURIC ACID
Hexethal (5-ethyl-5-hexylbarbituric acid)
NS00114036
2,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-hexyl-
Q27887323
5-Ethyl-5-hexyl-2-hydroxypyrimidine-4,6(1H,5H)-dione
pyrimidine-2,4,6(1H,3H,5H)-trione, 5-ethyl-5-hexyl-
Solubility of 5-ethyl-5-hexyl-hexahydropyrimidine-2,4,6-trione
The solubility of 5-ethyl-5-hexyl-hexahydropyrimidine-2,4,6-trione in various solvents can be influenced by several factors. Understanding its solubility properties is essential for applications in pharmaceuticals and organic chemistry.
Factors Influencing Solubility:
Although specific experimental data for solubility may be limited, it is common for compounds of this class to exhibit moderate to low solubility in water, while showing higher solubility in organic solvents such as dichloromethane or ethanol.
To illustrate the solubility behavior:
Typical Solvent Categories:
Understanding these solubility characteristics is vital for effective use in practical applications, allowing researchers to select the appropriate solvent for desired chemical reactions or formulations.