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CAS 4269-93-6

:

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

Description:
6-Bromopyrimidine-2,4(1H,3H)-dione, with the CAS number 4269-93-6, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is substituted with a bromine atom and two carbonyl groups. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents. The presence of the bromine atom introduces notable reactivity, making it a useful intermediate in various organic synthesis reactions, particularly in the development of pharmaceuticals and agrochemicals. The diketone functional groups contribute to its ability to participate in nucleophilic addition reactions and can also influence its biological activity. Additionally, the compound may exhibit tautomerism due to the keto-enol equilibrium, which can affect its chemical behavior and interactions. Overall, 6-bromopyrimidine-2,4(1H,3H)-dione is a valuable compound in synthetic organic chemistry, with applications in medicinal chemistry and material science.
Formula:C4H3BrN2O2
InChI:InChI=1/C4H3BrN2O2/c5-2-1-3(8)7-4(9)6-2/h1H,(H2,6,7,8,9)
SMILES:c1c(Br)nc(nc1O)O
Synonyms:
  • 2,4(1H,3H)-pyrimidinedione, 6-bromo-
  • 6-Bromopyrimidine-2,4(1H,3H)-dione
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