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Atomfair 1-(Trifluoromethylsulfonyl)piperidine C6H10F3NO2S
Description 1-(Trifluoromethylsulfonyl)piperidine (CAS No. 51029-15-3) is a high-purity organosulfur compound with the molecular formula C6H10F3NO2S . This specialized chemical features a piperidine ring substituted with a trifluoromethylsulfonyl group, offering unique reactivity and stability for advanced synthetic applications. With a molecular weight of 217.21 g/mol, this reagent is particularly valuable in pharmaceutical research, agrochemical development, and materials science due to its electron-withdrawing properties and ability to act as a versatile intermediate. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers under inert atmosphere to maintain integrity. Ideal for nucleophilic substitution reactions, catalysis studies, and…
Description
Description
1-(Trifluoromethylsulfonyl)piperidine (CAS No. 51029-15-3) is a high-purity organosulfur compound with the molecular formula C6H10F3NO2S. This specialized chemical features a piperidine ring substituted with a trifluoromethylsulfonyl group, offering unique reactivity and stability for advanced synthetic applications. With a molecular weight of 217.21 g/mol, this reagent is particularly valuable in pharmaceutical research, agrochemical development, and materials science due to its electron-withdrawing properties and ability to act as a versatile intermediate. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers under inert atmosphere to maintain integrity. Ideal for nucleophilic substitution reactions, catalysis studies, and as a building block for fluorinated compounds.
- CAS No: 51029-15-3
- Molecular Formula: C6H10F3NO2S
- Molecular Weight: 217.21
- Exact Mass: 217.03843422
- Monoisotopic Mass: 217.03843422
- IUPAC Name: 1-(trifluoromethylsulfonyl)piperidine
- SMILES: C1CCN(CC1)S(=O)(=O)C(F)(F)F
- Synonyms: 1-(trifluoromethylsulfonyl)piperidine, 51029-15-3, 1-((Trifluoromethyl)sulfonyl)piperidine, 1-[(trifluoromethyl)sulfonyl]piperidine, 1-(trifluoromethanesulfonyl)piperidine
Application
1-(Trifluoromethylsulfonyl)piperidine serves as a key intermediate in the synthesis of biologically active molecules, particularly in medicinal chemistry where the trifluoromethylsulfonyl moiety enhances metabolic stability. The compound finds utility as a precursor for N-containing heterocycles in pharmaceutical development, especially for CNS-targeting drugs. Its strong electron-withdrawing characteristics make it valuable in catalyst systems and as a reagent for introducing trifluoromethylsulfonyl groups in organic synthesis pipelines.
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