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CAS 898044-55-8

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4-Chloro-5-fluoro-6-methylpyrimidine

Description:
4-Chloro-5-fluoro-6-methylpyrimidine is a heterocyclic organic compound characterized by a pyrimidine ring substituted with chlorine, fluorine, and a methyl group. The presence of these halogen and alkyl substituents influences its chemical reactivity and physical properties. Typically, compounds of this nature exhibit moderate polarity due to the electronegative halogen atoms, which can also enhance their reactivity in nucleophilic substitution reactions. The methyl group contributes to the overall hydrophobic character of the molecule. This compound is often utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules, as the pyrimidine ring is a common scaffold in many drugs. Its unique substitution pattern can affect biological activity, making it a subject of interest in medicinal chemistry. Additionally, it may exhibit specific solubility characteristics in various solvents, which is crucial for its application in drug formulation. Safety data should be consulted for handling, as halogenated compounds can pose health risks.
Formula:C5H4ClFN2
InChI:InChI=1S/C5H4ClFN2/c1-3-4(7)5(6)9-2-8-3/h2H,1H3
InChI key:InChIKey=GHMKXPYBLNJQIK-UHFFFAOYSA-N
SMILES:FC=1C(C)=NC=NC1Cl
Synonyms:
  • Pyrimidine, 4-chloro-5-fluoro-6-methyl-
  • 4-Chloro-5-fluoro-6-methylpyrimidine
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