Interesting facts
Interesting Facts About 5-Ethyl-5-Isopropyl-Hexahydropyrimidine-2,4,6-Trione
5-Ethyl-5-isopropyl-hexahydropyrimidine-2,4,6-trione, a fascinating chemical compound, holds a unique position in organic chemistry due to its complex structure and diverse applications. Here are some intriguing insights into this compound:
- Structural Variety: This compound exhibits a remarkable structure characterized by a hexahydropyrimidine ring, showcasing the beauty of heterocyclic chemistry. The presence of multiple substituents, such as ethyl and isopropyl groups, contributes to its unique properties.
- Reactivity: The trione functional groups present in the structure can participate in various chemical reactions, making this compound an interesting subject for synthetic chemistry. It is known to react well with nucleophiles and has the potential to serve as a precursor for more complex molecules.
- Biological Relevance: Compounds with similar structures often exhibit significant biological activity. Research has highlighted that derivatives of pyrimidine are widely studied for their potential as pharmaceuticals. While specific studies on this compound might be scarce, it could inspire further explorations in medicinal chemistry.
- Applications: Due to its potential reactivity, it could find applications in agrochemicals, as intermediates in drug synthesis, or in materials science as a component of polymeric materials.
- Analytical Chemistry: Understanding and characterizing such compounds requires advanced analytical techniques. Spectroscopic methods such as NMR and IR spectroscopy play crucial roles in identifying the distinct functional groups and confirming structure.
"In the realm of organic compounds, the more complex the structure, the greater the potential for discovery."
This compound exemplifies a rich area of study where chemistry intersects with various applications, making it a compelling topic for both scientific research and educational pursuits.
Synonyms
PROBARBITAL
Probarbitone
Ipral
Vasalgin
Irenal
5-Ethyl-5-isopropylbarbituric acid
Ethylisopropylbarbituric acid
76-76-6
Isopropyl ethyl barbituric acid
Barbituric acid, 5-ethyl-5-isopropyl-
NSC 120742
5-ethyl-5-propan-2-yl-1,3-diazinane-2,4,6-trione
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-(1-methylethyl)-
R87TF75S6O
5-Ethyl-5-(1-methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
NSC-120742
BRN 0167241
UNII-R87TF75S6O
5-24-09-00159 (Beilstein Handbook Reference)
SCHEMBL715090
5-ethyl-5-isopropylpyrimidine-2,4,6(1h,3h,5h)-trione
CHEMBL2110696
DTXSID30226897
HHLXJTDUHFBYAU-UHFFFAOYSA-N
NSC120742
AKOS006273375
WLN: T6VMVMV FHJ FY1&1 F2
5-ETHYL-5-ISOPROPYL-BARBITURIC ACID
NS00114089
Q7246894
5-Ethyl-5-isopropyl-2,4,6(1H,3H,5H)-pyrimidinetrione #
2,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-(1-methylethyl)-
5-ETHYL-5-ISOPROPYLHEXAHYDROPYRIMIDINE-2,4,6-TRIONE
pyrimidine-2,4,6(1H,3H,5H)-trione, 5-ethyl-5-isopropyl-
Solubility of 5-ethyl-5-isopropyl-hexahydropyrimidine-2,4,6-trione
The solubility of 5-ethyl-5-isopropyl-hexahydropyrimidine-2,4,6-trione is an intriguing topic due to a variety of factors that govern its behavior in different solvents. Understanding its solubility can aid in predicting its applications and reactivity:
Moreover, in general terms, many complex organic compounds such as 5-ethyl-5-isopropyl-hexahydropyrimidine-2,4,6-trione often exhibit limited aqueous solubility due to their hydrophobic hydrocarbon chains. However, when assessing solubility, it can be advantageous to consider the following:
In conclusion, while specific data on 5-ethyl-5-isopropyl-hexahydropyrimidine-2,4,6-trione's solubility may be limited, understanding the underlying principles can lead to informed and effective use of this compound in various chemical contexts.