CAS 58713-03-4
:5-acetyl-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione
Description:
5-Acetyl-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione, with the CAS number 58713-03-4, is a heterocyclic organic compound characterized by a pyrimidine ring substituted with acetyl and dimethyl groups. This compound features a trione functional group, indicating the presence of three carbonyl (C=O) groups within its structure, which contributes to its reactivity and potential applications in organic synthesis. The presence of the acetyl group enhances its electrophilic character, making it useful in various chemical reactions, including condensation and acylation processes. The dimethyl substitutions on the pyrimidine ring can influence the compound's solubility and stability, as well as its interaction with biological systems. Typically, compounds of this nature may exhibit biological activity, making them of interest in medicinal chemistry. Overall, 5-acetyl-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione is a versatile compound with potential applications in pharmaceuticals and organic synthesis, owing to its unique structural features and functional groups.
Formula:C8H10N2O4
InChI:InChI=1/C8H10N2O4/c1-4(11)5-6(12)9(2)8(14)10(3)7(5)13/h5H,1-3H3
SMILES:CC(=O)C1C(=O)N(C)C(=O)N(C)C1=O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
5-Acetyl-1,3-dimethylbarbituric Acid
CAS:Formula:C8H10N2O4Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow powder to crystallineMolecular weight:198.185-acetyl-6-hydroxy-1,3-dimethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
CAS:Controlled Product<p>Applications 5-acetyl-6-hydroxy-1,3-dimethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (cas# 58713-03-4) is a useful research chemical.<br></p>Formula:C8H10N2O4Color and Shape:NeatMolecular weight:198.185-Acetyl-1,3-dimethylbarbituric
CAS:Formula:C8H10N2O4Purity:98%Color and Shape:SolidMolecular weight:198.176


