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Trifluoromethanesulfonamide, 96%
CAS: 421-85-2 | CH2F3NO2S | 149.09 g/mol
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Catalog number B22112.06
also known as B22112-06
Price (EUR)
254,15
Online Exclusive
299,00Save 44,85 (15%)
Each
Quantity:
5 g
Price (EUR)
254,15
Online Exclusive
299,00Save 44,85 (15%)
Each
Chemical Identifiers
CAS421-85-2
Specifications
Specification Sheet
Specification SheetAssay (Aqueous acid-base Titration)≥95.0 to ≤105.0%
Identification (FTIR)Conforms
Melting Point (clear melt)115.0-124.0?C
FormCrystals or powder or crystalline powder
Appearance (Color)White to pale cream
Trifluoromethanesulfonamide is used as an intermediate in synthetic chemistry. It is used in the preparation of specific inhibitors of mammalian secreted phospholipases A2. It is also involved in the synthesis of ecicosanoids.
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
Trifluoromethanesulfonamide is used as an intermediate in synthetic chemistry. It is used in the preparation of specific inhibitors of mammalian secreted phospholipases A2. It is also involved in the synthesis of ecicosanoids.
Solubility
Soluble in water.
Notes
Light sensitive. Incompatible with strong oxidizing agents, strong acid and bases.
Trifluoromethanesulfonamide is used as an intermediate in synthetic chemistry. It is used in the preparation of specific inhibitors of mammalian secreted phospholipases A2. It is also involved in the synthesis of ecicosanoids.
Solubility
Soluble in water.
Notes
Light sensitive. Incompatible with strong oxidizing agents, strong acid and bases.
RUO – Research Use Only
General References:
- Shainyan, B. A. Mono- and disubstituted highly unsaturated trifluoromethanesulfonamide derivatives. Theoretical analysis. Russ. J. Org. Chem. 2015, 51 (5), 605-609.
- Shainyan, B. A.; Ushakova, I. V.; Danilevich, Y. S. Bromination of highly unsaturated trifluoromethanesulfonamide derivatives. Russ. J. Org. Chem. 2015, 51 (7), 931-935.