Interesting facts
Interesting Facts about 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione
The compound 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione is a fascinating example of a synthetic organic molecule that showcases the complexity and creativity of modern chemistry. Here are some intriguing facts:
- Chemical Structure: This compound belongs to the class of hexahydropyrimidines, which are notable for their six-membered rings containing nitrogen atoms. The diverse substitutions on the pyrimidine ring contribute to its unique reactivity and potential applications.
- Bridging Compounds: The incorporation of the bromoallyl group enhances the molecule's ability to participate in various chemical reactions, such as nucleophilic substitutions, making it a valuable intermediate in organic synthesis.
- Potential Applications: Compounds like this one can serve as precursors for pharmaceuticals. Their structural features may lend themselves to bioactivity, potentially influencing *enzyme inhibition* or *antimicrobial activity*.
- Research Implications: Understanding the reactivity and synthesis of compounds such as this can contribute to the development of new methodologies in synthetic organic chemistry, paving the way for innovative *drug design* and *material science*.
- Chemical Stability: The stable nature of the hexahydropyrimidine ring makes it a subject of research for dynamic equilibrium and reaction pathways, providing insights into thermodynamics and kinetics in chemical reactions.
The study of compounds like 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione not only deepens our understanding of complex organic chemistry but also opens doors to future discoveries and applications in various scientific fields.
Synonyms
Sigmodal
1216-40-6
5-(2-Bromoallyl)-5-(1-methylbutyl)-1H,3H,5H-pyrimidine-2,4,6-trione
5-(2-bromoprop-2-enyl)-5-pentan-2-yl-1,3-diazinane-2,4,6-trione
8N609W64JZ
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(2-bromo-2-propenyl)-5-(1-methylbutyl)-
5-(.beta.-Bromoallyl)-5-(1-methylbutyl)barbituric acid
Recton
UNII-8N609W64JZ
EINECS 214-932-2
Barbituric acid, 5-(2-bromoallyl)-5-(1-methylbutyl)-
DTXSID90874338
5-(2-BROMOALLYL)-5-(1-METHYLBUTYL) BARBITURIC ACID
NS00010480
Q7512448
5-(2-Bromoallyl)-5-sec-pentyl-1H,3>H,5H-pyrimidine-2,4,6-trione
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 5-(2-BROMO-2-PROPEN-1-YL)-5-(1-METHYLBUTYL)-
5-(2-Bromo-2-propenyl)-5-(1-methylbutyl)-2,4,6(1H,3H,5H)-pyrimidinetrione #
Solubility of 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione
The solubility of 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione in various solvents can significantly influence its applications in chemical processes. Understanding the solubility behavior of this compound is crucial for its effective utilization.
Key Points on Solubility:
As stated, “Like dissolves like.” Thus, the solubility of this compound is highly dependent on the solvent's polarity. Experimentation and characterization through various solubility tests will provide valuable insights into its behavior in different environments.