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CAS 851986-00-0

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4,6-Dichloro-5-methoxy-2-methylpyrimidine

Description:
4,6-Dichloro-5-methoxy-2-methylpyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. This compound features two chlorine substituents at the 4 and 6 positions, a methoxy group (-OCH3) at the 5 position, and a methyl group (-CH3) at the 2 position. These substituents contribute to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of chlorine atoms enhances its lipophilicity and may influence its biological activity. The methoxy group can also participate in various chemical reactions, making this compound versatile in synthetic chemistry. Additionally, the compound's structure suggests potential for interactions with biological targets, which may be explored in drug development. As with many pyrimidine derivatives, it may exhibit interesting pharmacological properties, although specific biological activities would need to be investigated through empirical studies.
Formula:C6H6Cl2N2O
InChI:InChI=1S/C6H6Cl2N2O/c1-3-9-5(7)4(11-2)6(8)10-3/h1-2H3
InChI key:InChIKey=QGDCAAAIQWLPLQ-UHFFFAOYSA-N
SMILES:O(C)C=1C(Cl)=NC(C)=NC1Cl
Synonyms:
  • 4,6-Dichloro-5-methoxy-2-methylpyrimidine
  • Pyrimidine, 4,6-dichloro-5-methoxy-2-methyl-
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