Barbituric acid derivative
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- Molecular formula
- C12H22N2O3
- CAS Number
- 125-32-2
- IUPAC Name
- 5,5-dibutylhexahydropyrimidine-2,4,6-trione
- Molecular Weight
- 252.34g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2200g/cm3
- Synonyms
- 5, 5-Dibutylbarbituric acid
Identification
Interesting facts
Interesting Facts about 5,5-Dibutylhexahydropyrimidine-2,4,6-trione
5,5-Dibutylhexahydropyrimidine-2,4,6-trione is a fascinating compound in organic chemistry due to its unique structure and potential applications. Here are some intriguing aspects worth exploring:
- Structural Complexity: This compound features a hexahydropyrimidine ring, which is a characteristic structure that contributes to its reactivity and stability. Its formulation includes dibutyl groups, which greatly influence its physical and chemical properties.
- Diverse Applications: Compounds like 5,5-dibutylhexahydropyrimidine-2,4,6-trione are often studied for their potential use in pharmaceuticals and agrochemicals, making them important in both medicinal chemistry and agricultural science.
- Research Interest: Scientists are intrigued by its potential biological activities. Research indicates that compounds of similar structural frameworks may exhibit important roles such as antibacterial or antifungal properties.
- Synthetic Pathways: Understanding the synthetic routes to create this compound is essential, as it can underscore methods of functionalization and introduce innovative approaches in synthetic organic chemistry.
- Functional Groups: The presence of the ketone groups in the trione structure presents opportunities for further reactions, such as nucleophilic attacks, which are fundamental in the formation of more complex substances.
As we continue to explore the realm of chemical compounds like 5,5-dibutylhexahydropyrimidine-2,4,6-trione, we uncover their potential implications across various scientific fields. Understanding these molecules not only enriches our knowledge but also opens doors to future innovations.