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Atomfair S-(Trifluoromethyl) benzenesulfonothioate C7H5F3O2S2
Description S-(Trifluoromethyl) benzenesulfonothioate (CAS No. 15398-96-6) is a high-purity organosulfur compound with the molecular formula C7H5F3O2S2. This specialty chemical, also known by its IUPAC name trifluoromethylsulfanylsulfonylbenzene , features a unique trifluoromethylthio (-SCF3) group bonded to a benzenesulfonyl moiety, making it a valuable building block in synthetic organic chemistry and materials science. The compound is supplied as a stable, crystalline solid with ??95% purity (GC), ideal for research applications requiring precise electrophilic or nucleophilic reactivity. Its distinct molecular architecture offers exceptional potential as a fluorinated synthon for pharmaceutical intermediates, agrochemical development, and advanced material modification. Proper storage at 2-8??C under inert…
Description
Description
S-(Trifluoromethyl) benzenesulfonothioate (CAS No. 15398-96-6) is a high-purity organosulfur compound with the molecular formula C7H5F3O2S2. This specialty chemical, also known by its IUPAC name trifluoromethylsulfanylsulfonylbenzene, features a unique trifluoromethylthio (-SCF3) group bonded to a benzenesulfonyl moiety, making it a valuable building block in synthetic organic chemistry and materials science. The compound is supplied as a stable, crystalline solid with ??95% purity (GC), ideal for research applications requiring precise electrophilic or nucleophilic reactivity. Its distinct molecular architecture offers exceptional potential as a fluorinated synthon for pharmaceutical intermediates, agrochemical development, and advanced material modification. Proper storage at 2-8??C under inert atmosphere is recommended to maintain optimal stability.
- CAS No: 15398-96-6
- Molecular Formula: C7H5F3O2S2
- Molecular Weight: 242.2
- Exact Mass: 241.96830623
- Monoisotopic Mass: 241.96830623
- IUPAC Name: trifluoromethylsulfanylsulfonylbenzene
- SMILES: C1=CC=C(C=C1)S(=O)(=O)SC(F)(F)F
- Synonyms: S-(Trifluoromethyl) benzenesulfonothioate, 15398-96-6, Benzenethiosulfonic acid S-(trifluoromethyl) ester, SCHEMBL11130216, VJKJRLIFMWSBNO-UHFFFAOYSA-N
Application
S-(Trifluoromethyl) benzenesulfonothioate serves as a versatile reagent for introducing trifluoromethylthio groups into organic molecules, a critical modification in drug discovery for enhancing metabolic stability and lipophilicity. Researchers utilize this compound in nucleophilic substitution reactions to create novel fluorinated compounds with potential bioactivity. The sulfonothioate moiety also finds application in polymer chemistry as a chain transfer agent or crosslinking modifier for specialty materials. Its unique reactivity profile makes it particularly valuable in developing PET radiotracers and other fluorine-containing imaging agents.
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