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CAS 4840-69-1

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5-Fluoro-3-methyl-1H-pyrimidine-2,4-dione

Description:
5-Fluoro-3-methyl-1H-pyrimidine-2,4-dione, with the CAS number 4840-69-1, is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a fluorine atom and a methyl group. This compound features two carbonyl groups at the 2 and 4 positions of the pyrimidine ring, contributing to its diketone structure. The presence of the fluorine atom enhances its reactivity and can influence its biological activity, making it of interest in medicinal chemistry. The methyl group at the 3 position can affect the compound's steric and electronic properties, potentially impacting its interactions with biological targets. Typically, compounds of this nature exhibit moderate to high solubility in polar solvents and may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Its unique structure allows for potential applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. As with many heterocycles, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature.
Formula:C5H5FN2O2
InChI:InChI=1/C5H5FN2O2/c1-8-4(9)3(6)2-7-5(8)10/h2H,1H3,(H,7,10)
SMILES:Cn1c(=O)c(cnc1O)F
Synonyms:
  • 2,4(1H,3H)-pyrimidinedione, 5-fluoro-3-methyl-
  • 5-Fluoro-3-methylpyrimidine-2,4(1H,3H)-dione
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