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Atomfair (4-Methyl-3-nitrophenyl) trifluoromethanesulfonate C8H6F3NO5S

Description (4-Methyl-3-nitrophenyl) trifluoromethanesulfonate (CAS No. 195455-54-0) is a high-purity organic sulfonate ester with the molecular formula C8H6F3NO5S . This compound features a trifluoromethanesulfonate (triflate) group attached to a 4-methyl-3-nitrophenyl backbone, making it a valuable reagent in synthetic organic chemistry and pharmaceutical research. Its excellent leaving group properties and electron-withdrawing nitro substituent enhance its reactivity in nucleophilic substitution and cross-coupling reactions. Ideal for laboratory use, this product is rigorously tested for purity and stability, ensuring reliable performance in demanding applications. Packaged under inert conditions to maintain integrity, it is suitable for use in advanced chemical synthesis and material science research.

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Description

Description

(4-Methyl-3-nitrophenyl) trifluoromethanesulfonate (CAS No. 195455-54-0) is a high-purity organic sulfonate ester with the molecular formula C8H6F3NO5S. This compound features a trifluoromethanesulfonate (triflate) group attached to a 4-methyl-3-nitrophenyl backbone, making it a valuable reagent in synthetic organic chemistry and pharmaceutical research. Its excellent leaving group properties and electron-withdrawing nitro substituent enhance its reactivity in nucleophilic substitution and cross-coupling reactions. Ideal for laboratory use, this product is rigorously tested for purity and stability, ensuring reliable performance in demanding applications. Packaged under inert conditions to maintain integrity, it is suitable for use in advanced chemical synthesis and material science research.

  • CAS No: 195455-54-0
  • Molecular Formula: C8H6F3NO5S
  • Molecular Weight: 285.20
  • Exact Mass: 284.99187795
  • Monoisotopic Mass: 284.99187795
  • IUPAC Name: (4-methyl-3-nitrophenyl) trifluoromethanesulfonate
  • SMILES: CC1=C(C=C(C=C1)OS(=O)(=O)C(F)(F)F)[N+](=O)[O-]

Application

(4-Methyl-3-nitrophenyl) trifluoromethanesulfonate is widely used as a versatile intermediate in organic synthesis, particularly in the preparation of aryl triflates for palladium-catalyzed cross-coupling reactions. Its robust reactivity makes it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. Researchers also employ it in the study of reaction mechanisms involving sulfonate esters. The electron-withdrawing nitro group further enhances its utility in electrophilic aromatic substitution reactions.

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