CAS 66941-74-0
:5-(2-methylprop-2-en-1-yl)-5-(prop-2-en-1-yl)pyrimidine-2,4,6(1H,3H,5H)-trione
Description:
5-(2-methylprop-2-en-1-yl)-5-(prop-2-en-1-yl)pyrimidine-2,4,6(1H,3H,5H)-trione, with the CAS number 66941-74-0, is a synthetic organic compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing nitrogen atoms. This compound features two alkenyl substituents, specifically isopropenyl groups, at the 5-position of the pyrimidine ring, contributing to its reactivity and potential applications in organic synthesis. The presence of the trione functional groups indicates that it contains three carbonyl groups, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The compound's structure suggests it may exhibit interesting biological activities, making it a candidate for further research in medicinal chemistry. Its stability, solubility, and reactivity would depend on the specific conditions and solvents used in experiments. Overall, this compound represents a unique structure within the realm of pyrimidine derivatives, with potential implications in various fields of chemistry and pharmacology.
Formula:C11H14N2O3
InChI:InChI=1/C11H14N2O3/c1-4-5-11(6-7(2)3)8(14)12-10(16)13-9(11)15/h4H,1-2,5-6H2,3H3,(H2,12,13,14,15,16)
SMILES:C=CCC1(CC(=C)C)C(=NC(=O)N=C1O)O
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Found 4 products.
5-Allyl-5-methallyl-barbituric Acid
CAS:Controlled ProductFormula:C11H14N2O3Color and Shape:NeatMolecular weight:222.245-Allyl-5-methallyl-barbituric Acid (1 mg/ml in Acetonitrile)
CAS:Controlled ProductFormula:C11H14N2O3Color and Shape:Single SolutionMolecular weight:222.245-Allyl-5-methallyl-barbituric acid
CAS:Controlled ProductPlease enquire for more information about 5-Allyl-5-methallyl-barbituric acid including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C11H14N2O3Purity:Min. 95%Molecular weight:222.24 g/mol


