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CAS 56177-80-1

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2-Ethoxy-5-fluoro-4(3H)-pyrimidinone

Description:
2-Ethoxy-5-fluoro-4(3H)-pyrimidinone is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of an ethoxy group at the 2-position and a fluorine atom at the 5-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar organic solvents due to the ethoxy group, which enhances its solubility profile. The fluorine substituent can influence the compound's reactivity and biological activity, making it of interest in pharmaceutical research. Additionally, the presence of the pyrimidinone moiety suggests potential applications in medicinal chemistry, particularly in the development of antiviral or anticancer agents. Its molecular structure allows for various chemical reactions, including nucleophilic substitutions and potential interactions with biological targets. As with many fluorinated compounds, it may exhibit enhanced metabolic stability and altered pharmacokinetics compared to its non-fluorinated counterparts.
Formula:C6H7FN2O2
InChI:InChI=1S/C6H7FN2O2/c1-2-11-6-8-3-4(7)5(10)9-6/h3H,2H2,1H3,(H,8,9,10)
InChI key:InChIKey=XREDGJFKPWBNRQ-UHFFFAOYSA-N
SMILES:O(CC)C=1NC(=O)C(F)=CN1
Synonyms:
  • 2-Ethoxy-5-fluoro-1,4-dihydropyrimidin-4-one
  • 2-Ethoxy-5-fluoro-1H-pyrimidin-4-one
  • 2-Ethoxy-5-fluoro-1H-pyrimidin-6-one
  • 2-Ethoxy-5-fluoro-3,4-dihydropyrimidin-4-one
  • 2-Ethoxy-5-fluoropyrimidin-4-ol
  • 2-Ethoxy-5-fluorouracil
  • 2-ethoxy-5-fluoropyrimidin-4(3H)-one
  • 4(1H)-Pyrimidinone, 2-ethoxy-5-fluoro-
  • 4(3H)-Pyrimidinone, 2-ethoxy-5-fluoro-
  • 2-Ethoxy-5-fluoro-4(3H)-pyrimidinone
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