Atomfair Difluoromethanesulfinyl chloride CHClF2OS

Description Difluoromethanesulfinyl chloride (CAS No. 1858131-42-6) is a highly specialized organosulfur compound with the molecular formula CHClF2OS . This reagent is a valuable building block in synthetic organic chemistry, particularly for the introduction of the difluoromethanesulfinyl moiety into target molecules. Its unique structure, featuring both sulfinyl and chloro-difluoromethyl functional groups, makes it an ideal candidate for nucleophilic substitution reactions and electrophilic fluorination processes. The compound is supplied as a high-purity liquid, rigorously tested for consistency and quality, ensuring optimal performance in sensitive applications. Proper storage under inert conditions is recommended to maintain stability.

Description

Description

Difluoromethanesulfinyl chloride (CAS No. 1858131-42-6) is a highly specialized organosulfur compound with the molecular formula CHClF2OS. This reagent is a valuable building block in synthetic organic chemistry, particularly for the introduction of the difluoromethanesulfinyl moiety into target molecules. Its unique structure, featuring both sulfinyl and chloro-difluoromethyl functional groups, makes it an ideal candidate for nucleophilic substitution reactions and electrophilic fluorination processes. The compound is supplied as a high-purity liquid, rigorously tested for consistency and quality, ensuring optimal performance in sensitive applications. Proper storage under inert conditions is recommended to maintain stability.

  • CAS No: 1858131-42-6
  • Molecular Formula: CHClF2OS
  • Molecular Weight: 134.53
  • Exact Mass: 133.9404698
  • Monoisotopic Mass: 133.9404698
  • IUPAC Name: difluoromethanesulfinyl chloride
  • SMILES: C(F)(F)S(=O)Cl
  • Synonyms: Difluoromethanesulfinyl chloride, 1858131-42-6, Difluoromethanesulfinylchloride, SCHEMBL15940672, KXTLHJHZGXFCMO-UHFFFAOYSA-N

Application

Difluoromethanesulfinyl chloride is primarily used as a key intermediate in pharmaceutical and agrochemical research, enabling the synthesis of fluorinated analogs with enhanced bioactivity. It serves as a versatile electrophile in the preparation of sulfoxides and sulfinamides, critical motifs in medicinal chemistry. Researchers also employ it in the development of novel fluorinated polymers and materials with tailored properties.

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