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Atomfair 4-Fluorophenyl 4-methylbenzene-1-sulfonate C13H11FO3S

Description 4-Fluorophenyl 4-methylbenzene-1-sulfonate (CAS No. 1582-01-0) is a high-purity sulfonate ester compound with the molecular formula C13H11FO3S . This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique reactivity as a sulfonating agent. The compound features a fluorophenyl group and a toluenesulfonate moiety, offering versatile applications in cross-coupling reactions and as a building block for advanced intermediates. Our product is rigorously tested to ensure ??95% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for researchers seeking reliable, high-quality reagents for method development and scale-up processes.

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Description

Description

4-Fluorophenyl 4-methylbenzene-1-sulfonate (CAS No. 1582-01-0) is a high-purity sulfonate ester compound with the molecular formula C13H11FO3S. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique reactivity as a sulfonating agent. The compound features a fluorophenyl group and a toluenesulfonate moiety, offering versatile applications in cross-coupling reactions and as a building block for advanced intermediates. Our product is rigorously tested to ensure ??95% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for researchers seeking reliable, high-quality reagents for method development and scale-up processes.

  • CAS No: 1582-01-0
  • Molecular Formula: C13H11FO3S
  • Molecular Weight: 266.29
  • Exact Mass: 266.04129354
  • Monoisotopic Mass: 266.04129354
  • IUPAC Name: (4-fluorophenyl) 4-methylbenzenesulfonate
  • SMILES: CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=C(C=C2)F
  • Synonyms: SCHEMBL4126119, 4-fluorophenyl 4-methylbenzene-1-sulfonate, EN300-7078411

Application

4-Fluorophenyl 4-methylbenzene-1-sulfonate serves as a key intermediate in the synthesis of fluorinated aromatic compounds and sulfonamide derivatives. It is particularly valuable in pharmaceutical research for constructing bioactive molecules with enhanced metabolic stability. The compound’s sulfonate group also facilitates polymerization reactions in specialty material science applications.

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