1-Phenylpyrimidine-2,4,6(1H,3H,5H)-trione, with the CAS number 15018-50-5, is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a phenyl group and three carbonyl groups at positions 2, 4, and 6. This compound exhibits properties typical of pyrimidine derivatives, including potential biological activity and applications in medicinal chemistry. The presence of multiple carbonyl groups contributes to its reactivity, making it a candidate for various chemical transformations. It may also participate in hydrogen bonding due to the presence of nitrogen atoms in the ring, influencing its solubility and interaction with other molecules. The compound's structure suggests potential uses in the synthesis of pharmaceuticals or agrochemicals, as well as in research related to nucleic acid chemistry. Its stability and reactivity can vary depending on the conditions, such as pH and solvent, which are important considerations for its practical applications. Overall, 1-phenylpyrimidine-2,4,6(1H,3H,5H)-trione is a versatile compound with significant implications in organic synthesis and medicinal chemistry.

1-phenylpyrimidine-2,4,6(1H,3H,5H)-trione

15018-50-5: 1-Phenylpyrimidine-2,4,6(1H,3H,5H)-trione, with the CAS number 15018-50-5, is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a phenyl group and three carbonyl groups at positions 2, 4, and 6. This compound exhibits properties typical of pyrimidine derivatives, including potential biological activity and applications in medicinal chemistry. The presence of multiple carbonyl groups contributes to its reactivity, making it a candidate for various chemical transformations. It may also participate in hydrogen bonding due to the presence of nitrogen atoms in the ring, influencing its solubility and interaction with other molecules. The compound's structure suggests potential uses in the synthesis of pharmaceuticals or agrochemicals, as well as in research related to nucleic acid chemistry. Its stability and reactivity can vary depending on the conditions, such as pH and solvent, which are important considerations for its practical applications. Overall, 1-phenylpyrimidine-2,4,6(1H,3H,5H)-trione is a versatile compound with significant implications in organic synthesis and medicinal chemistry.

1-Phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione

CAS 15018-50-5

1-phenylpyrimidine-2,4,6(1H,3H,5H)-trione

1-Phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione

Ref: 54-OR1002495

1-Phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione

Ref: 10-F612805