6-Phenyl-2,4(1H,3H)-pyrimidinedione, also known by its CAS number 13345-09-0, is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a phenyl group and two carbonyl groups. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents. Its structure features a bicyclic system that contributes to its potential biological activity, making it of interest in medicinal chemistry. The presence of the phenyl group can enhance lipophilicity, potentially influencing its pharmacokinetic properties. Additionally, the carbonyl functionalities may participate in hydrogen bonding and other interactions, which can affect its reactivity and binding affinity in biological systems. 6-Phenyl-2,4(1H,3H)-pyrimidinedione may also exhibit various chemical properties, including the ability to undergo tautomerization and participate in electrophilic substitution reactions. Overall, this compound's unique structural features make it a subject of interest for further research in drug development and synthetic chemistry.

6-Phenyl-2,4(1H,3H)-pyrimidinedione

13345-09-0: 2,4(1H,3H)-Pyrimidinedione, 6-phenyl-, 2,4-Dihydroxy-6-phenylpyrimidine, 6-Phenyl-2,4(1H,3H)-pyrimidinedione, 6-Phenylpyrimidin-2,4-diol, 6-phenylpyrimidine-2,4(1H,3H)-dione, Ai3-26585, NSC 49019, Uracil, 6-phenyl-, 6-Phenyluracil

6-Phenylpyrimidine-2,4(1H,3H)-dione

6-Phenyl-pyrimidine-2,4-diol is a cyclobutane that can be found in acidic solutions. It can also be found as an enantiomeric mixture of the two stereoisomers, which are the result of a dimerisation reaction. The hydrated form of this molecule has been shown to react with nucleic acids and nucleobases. 6-Phenyl-pyrimidine-2,4-diol can be used as a precursor to form other molecules.

CAS 13345-09-0: 6-Phenyl-2,4(1H,3H)-pyrimidinedione

6-Phenylpyrimidine-2,4(1H,3H)-dione

Ref: IN-DA007NFB

6-Phenyl-pyrimidine-2,4-diol

Ref: 3D-NAA34509

6-Phenyl-pyrimidine-2,4-diol

Ref: 10-F316927

6-Phenyl-pyrimidine-2,4-diol

Ref: 54-OR346181