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CAS 179260-78-7

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4-Methyl-2-(trifluoromethanesulfonyl)Oxypyridine

Description:
4-Methyl-2-(trifluoromethanesulfonyl)oxypyridine is a chemical compound characterized by its pyridine ring structure, which is substituted at the 2-position with a trifluoromethanesulfonyl group and at the 4-position with a methyl group. This compound is notable for its strong electron-withdrawing trifluoromethanesulfonyl group, which enhances its reactivity and potential applications in various chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals. The presence of the methyl group contributes to its hydrophobic characteristics, influencing its solubility and interaction with biological systems. Additionally, the trifluoromethanesulfonyl moiety is known for its stability and ability to participate in nucleophilic substitution reactions. Overall, 4-Methyl-2-(trifluoromethanesulfonyl)oxypyridine is a versatile compound with significant implications in organic synthesis and medicinal chemistry, although handling precautions are necessary due to the toxicity associated with trifluoromethanesulfonyl derivatives.
Formula:C7H6F3NO3S
InChI:InChI=1/C7H6F3NO3S/c1-5-2-3-11-6(4-5)14-15(12,13)7(8,9)10/h2-4H,1H3
SMILES:Cc1ccnc(c1)OS(=O)(=O)C(F)(F)F
Synonyms:
  • 4-Methyl-2-pyridyl Trifluoromethanesulfonate
  • Trifluoromethanesulfonic Acid 4-Methyl-2-pyridyl Ester
  • 4-Methylpyridin-2-Yl Trifluoromethanesulfonate
  • 4-Methyl-2-(trifluoromethanesulfonyl)Oxypyridine ISO 9001：2015 REACH
  • Methanesulfonic acid, 1,1,1-trifluoro-, 4-methyl-2-pyridinyl ester
  • Methanesulfonic acid, trifluoro-, 4-Methyl-2-pyridinyl ester
  • 4-Methyl-2-pyridylTrifluoromethanesulfonate&gt
  • 4-Methyl-2-(trifluoromethanesulfonyl)Oxypyridine
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