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CAS 1353973-60-0

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6-Chloro-N-methyl-2-(methylsulfonyl)-4-pyrimidinamine

Description:
6-Chloro-N-methyl-2-(methylsulfonyl)-4-pyrimidinamine 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 a chlorine atom at the 6-position and a methylsulfonyl group at the 2-position contributes to its unique reactivity and solubility properties. The N-methyl substitution enhances its lipophilicity, potentially influencing its biological activity. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological targets. Its molecular structure suggests potential applications in areas such as anti-infective or anti-cancer therapies, although specific biological activities would require empirical investigation. Additionally, the compound's stability, solubility, and reactivity can be influenced by environmental factors, making it important to consider these characteristics in practical applications. Safety and handling protocols should be observed, as with any chemical substance, to mitigate risks associated with its use.
Formula:C6H8ClN3O2S
InChI:InChI=1S/C6H8ClN3O2S/c1-8-5-3-4(7)9-6(10-5)13(2,11)12/h3H,1-2H3,(H,8,9,10)
InChI key:InChIKey=KZNZMBWUAGLCRI-UHFFFAOYSA-N
SMILES:S(C)(=O)(=O)C=1N=C(NC)C=C(Cl)N1
Synonyms:
  • 4-Pyrimidinamine, 6-chloro-N-methyl-2-(methylsulfonyl)-
  • 6-Chloro-N-methyl-2-(methylsulfonyl)-4-pyrimidinamine
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