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Atomfair 3-Fluoroprop-1-yl toluene-4-sulphonate C10H13FO3S

Description 3-Fluoropropyl p-toluenesulfonate (CAS 312-68-5) is a high-purity sulfonate ester compound with the molecular formula C10H13FO3S. This specialized chemical is widely utilized in organic synthesis, particularly as an alkylating agent or intermediate in pharmaceutical and materials science research. The compound features a fluoropropyl group linked to a toluenesulfonate moiety, offering unique reactivity for nucleophilic substitution reactions. Our product is rigorously tested to ensure >98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging under inert atmosphere to maintain stability. Ideal for researchers developing fluorinated compounds or investigating sulfonate chemistry.

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Description

Description

3-Fluoropropyl p-toluenesulfonate (CAS 312-68-5) is a high-purity sulfonate ester compound with the molecular formula C10H13FO3S. This specialized chemical is widely utilized in organic synthesis, particularly as an alkylating agent or intermediate in pharmaceutical and materials science research. The compound features a fluoropropyl group linked to a toluenesulfonate moiety, offering unique reactivity for nucleophilic substitution reactions. Our product is rigorously tested to ensure >98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging under inert atmosphere to maintain stability. Ideal for researchers developing fluorinated compounds or investigating sulfonate chemistry.

  • CAS No: 312-68-5
  • Molecular Formula: C10H13FO3S
  • Molecular Weight: 232.27
  • Exact Mass: 232.05694361
  • Monoisotopic Mass: 232.05694361
  • IUPAC Name: 3-fluoropropyl 4-methylbenzenesulfonate
  • SMILES: CC1=CC=C(C=C1)S(=O)(=O)OCCCF
  • Synonyms: 3-Fluoroprop-1-yl toluene-4-sulphonate, 695-356-2, 3-fluoropropyl 4-methylbenzenesulfonate, 312-68-5, 3-Fluoropropyl p-toluenesulfonate

Application

3-Fluoropropyl p-toluenesulfonate serves as a versatile building block in medicinal chemistry for introducing fluoropropyl groups into target molecules. Researchers employ this compound in the synthesis of fluorinated analogs for drug development and PET tracer candidates. The sulfonate ester functionality makes it particularly valuable for creating prodrugs or modifying biomolecules through selective alkylation reactions.

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