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CAS 1289386-28-2

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4-Chloro-6-ethoxy-2-(methylsulfinyl)pyrimidine

Description:
4-Chloro-6-ethoxy-2-(methylsulfinyl)pyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is a six-membered ring containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at position 4 and an ethoxy group at position 6 contributes to its chemical reactivity and solubility properties. Additionally, the methylsulfinyl group at position 2 introduces a sulfoxide functionality, which can influence the compound's biological activity and polarity. This compound is typically synthesized through specific organic reactions that involve the introduction of these substituents onto the pyrimidine core. It may exhibit various pharmacological properties, making it of interest in medicinal chemistry. The compound's molecular structure suggests potential applications in agrochemicals or pharmaceuticals, particularly in the development of new therapeutic agents. As with many organic compounds, its stability, reactivity, and interactions with other substances are influenced by the functional groups present.
Formula:C7H9ClN2O2S
InChI:InChI=1S/C7H9ClN2O2S/c1-3-12-6-4-5(8)9-7(10-6)13(2)11/h4H,3H2,1-2H3
InChI key:InChIKey=FYIAPGSVAJFRDH-UHFFFAOYSA-N
SMILES:O(CC)C1=NC(S(C)=O)=NC(Cl)=C1
Synonyms:
  • 4-Chloro-6-ethoxy-2-(methylsulfinyl)pyrimidine
  • Pyrimidine, 4-chloro-6-ethoxy-2-(methylsulfinyl)-
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