CAS 2518-72-1
:5-Ethyl-2,4,6(1H,3H,5H)-pyrimidinetrione
Description:
5-Ethyl-2,4,6(1H,3H,5H)-pyrimidinetrione, identified by its CAS number 2518-72-1, is a heterocyclic organic compound featuring a pyrimidine ring with three carbonyl groups and an ethyl substituent. This compound is characterized by its trione structure, which contributes to its reactivity and potential applications in various chemical reactions. The presence of the ethyl group enhances its lipophilicity, influencing its solubility and interaction with biological systems. Pyrimidinetriones are known for their ability to participate in hydrogen bonding due to the carbonyl functionalities, which can affect their stability and reactivity. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Additionally, its structural features allow for potential modifications, leading to derivatives with varied properties. Overall, 5-Ethyl-2,4,6(1H,3H,5H)-pyrimidinetrione is a versatile compound with implications in both synthetic chemistry and medicinal applications.
Formula:C6H8N2O3
InChI:InChI=1S/C6H8N2O3/c1-2-3-4(9)7-6(11)8-5(3)10/h3H,2H2,1H3,(H2,7,8,9,10,11)
InChI key:InChIKey=FMTLDVACNZDTQL-UHFFFAOYSA-N
SMILES:C(C)C1C(=O)NC(=O)NC1=O
Synonyms:- 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-
- 5-Ethyl-1,3-Diazinane-2,4,6-Trione
- 5-Ethyl-2,4,6(1H,3H,5H)-pyrimidinetrione
- 5-ethylpyrimidine-2,4,6(1H,3H,5H)-trione
- Barbituric acid, 5-ethyl-
- NSC 27274
- NSC 66908
- 5-Ethylbarbituric acid
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Found 3 products.
5-ethyl-6-hydroxy-1,2,3,4-tetrahydropyrimidine-2,4-dione
CAS:Formula:C6H8N2O3Color and Shape:SolidMolecular weight:156.13935-Ethylbarbituric Acid
CAS:Controlled Product<p>Applications 5-Ethylbarbituric Acid is an non-nucleoside inhibitors of HIV-1 reverse transcriptase.<br>References Mitchell, M. L., et al.: Bioorg. Med. Chem. Lett., 20, 1589 (2010); Al-Turkistani, A., et al.: Molecules., 16, 4764 (2011);<br></p>Formula:C6H8N2O3Color and Shape:NeatMolecular weight:156.14


