5-Bromo-4,6(1H,5H)-pyrimidinedione, with the CAS number 52176-13-3, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both bromine and carbonyl functional groups. This compound typically appears as a crystalline solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its ability to act as a building block in the synthesis of various biologically active molecules. The presence of the bromine atom enhances its reactivity, making it useful in substitution reactions. Additionally, the carbonyl groups contribute to its ability to participate in hydrogen bonding, influencing its solubility and reactivity in different solvents. The compound's stability and reactivity can be affected by environmental conditions such as pH and temperature. Overall, 5-Bromo-4,6(1H,5H)-pyrimidinedione is a valuable compound in organic synthesis and medicinal chemistry, with ongoing research exploring its full potential and applications.

5-Bromo-4,6(1H,5H)-pyrimidinedione

52176-13-3: 4,6(1H,5H)-Pyrimidinedione, 5-bromo-, 5-bromopyrimidine-4,6(1H,5H)-dione, 5-Bromo-4,6(1H,5H)-pyrimidinedione,  5-Bromo-1H,5H-pyrimidine-4,6-dione

5-Bromopyrimidine-4,6(1H,5H)-dione is a novel nucleoside analogue. It can be used as an antiviral agent and an anticancer drug. It inhibits viral DNA replication by competitively binding to the viral DNA polymerase, thereby blocking the incorporation of deoxyribonucleotides into the growing DNA chain. 5-Bromopyrimidine-4,6(1H,5H)-dione also has antitumour activity. It has been shown to inhibit the growth of human cancer cells in vitro and in vivo.

CAS 52176-13-3: 5-Bromo-4,6(1H,5H)-pyrimidinedione

5-Bromopyrimidine-4,6(1H,5H)-dione

Ref: 3D-NB44313

5-bromo-1H,5H-pyrimidine-4,6-dione

Ref: IN-DA00DI2C