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Trifluoromethanesulfonic anhydride, 98%, Thermo Scientific Chemicals

Alfa Aesar Trifluoromethanesulfonic anhydride, 98%, Quantity: 250g, Boiling Point: 81 deg.C to 83 deg.C, Melting Point: -80 deg.C, Molecular Weight: 282.127, Percent Purity: 98%, Beilstein: 1813600, CAS: 358-23-6, ChEBI: CHEBI:48509, Density: 1.72

£58.79 - £723.60

Chemical Identifiers

CAS 358-23-6
Molecular Formula C2F6O5S2
Molecular Weight (g/mol) 282.127
MDL Number MFCD00000408
InChI Key WJKHJLXJJJATHN-UHFFFAOYSA-N
Synonym trifluoromethanesulfonic anhydride, triflic anhydride, trifluoromethanesulphonic anhydride, trifluoromethanesulfonic acid anhydride, methanesulfonic acid, trifluoro-, anhydride, trifluoromethanesulphonic acid anhydride, unii-8w034lhg1u, tf2o, trifluoromethane sulfonyl trifluoromethanesulfonate, trifluoromethane sulfonic anhydride
PubChem CID 67749
ChEBI CHEBI:48509
IUPAC Name trifluoromethylsulfonyl trifluoromethanesulfonate
SMILES C(F)(F)(F)S(=O)(=O)OS(=O)(=O)C(F)(F)F
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A11767.09
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Description

Description

Trifluoromethanesulfonic anhydride is used to convert phenols and imine into triflic ester and NTf group. It is a strong electrophile used for the introduction of triflyl group in chemical synthesis. It serves as a reagent in the preparation of alkyl and vinyl triflates, and for the stereoselective synthesis of mannosazide methyl uronate donors. It acts as a catalyst for glycosylation with anomeric hydroxy sugars to prepare polysaccharides.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Trifluoromethanesulfonic anhydride is used to convert phenols and imine into triflic ester and NTf group. It is a strong electrophile used for the introduction of triflyl group in chemical synthesis. It serves as a reagent in the preparation of alkyl and vinyl triflates, and for the stereoselective synthesis of mannosazide methyl uronate donors. It acts as a catalyst for glycosylation with anomeric hydroxy sugars to prepare polysaccharides.

Solubility
Miscible with dichloromethane. Immiscible with hydrocarbons.

Notes
Moisture sensitive. Incompatible with water, strong bases, strong oxidizing agents, acids and alcohols.
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