
CAS 2923-16-2: Acetic acid, 2,2,2-trifluoro-, potassium salt (1:1)
Formula:C2HF3O2·K
InChI:InChI=1S/C2HF3O2.K/c3-2(4,5)1(6)7;/h(H,6,7);
InChI key:InChIKey=SIMZKPFFQPBRPY-UHFFFAOYSA-N
SMILES:C(C(O)=O)(F)(F)F.[K]
Synonyms:- Acetic acid, 2,2,2-trifluoro-, potassium salt (1:1)
- Acetic acid, trifluoro-, potassium salt
- Potasium Trifluoroacetate
- Potassiumtrifluoroacetate
- Trifluoroacetic Acid Potassium
- Trifluoroacetic Acid Potassium Salt
- Potassium trifluoroacetate
- potassium,2,2,2-trifluoroacetate
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Found 6 products.
Potassium trifluoroacetate, 98%
CAS:It is a reagent for preparation of aryl trifluoromethyl sulfides, by heating with the diaryl disulfide. 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.Formula:CF3CO2KPurity:98%Color and Shape:Crystals or powder or crystalline powder or lumps, WhiteMolecular weight:152.12Potassium Trifluoroacetate
CAS:Formula:C2F3KO2Purity:>98.0%(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:152.11Acetic acid, 2,2,2-trifluoro-, potassium salt (1:1)
CAS:Formula:C2F3KO2Purity:98%Color and Shape:SolidMolecular weight:152.1137Potassium Trifluoroacetate
CAS:Controlled ProductStability Very Hygroscopic Applications Potassium trifluoroacetate (cas# 2923-16-2) is a useful research chemical.Formula:C2F3KO2Color and Shape:NeatMolecular weight:152.11Trifluoroacetic acid, potassium salt
CAS:Purity:98.0%Color and Shape:Solid, Crystalline or PowderMolecular weight:152.11399841308594Potassium 2,2,2-trifluoroacetate
CAS:Potassium 2,2,2-trifluoroacetate (PTFAA) is a chemical compound that participates in a variety of reactions. It is used in the preparation of fatty acids and alcohols for analytical chemistry and as an intermediate in the synthesis of pharmaceuticals. PTFAA also has been shown to be effective at removing calcium stearate from samples. The reaction mechanism for PTFA is believed to involve nucleophilic attack by the trifluoroacetic acid on the carbonyl group of the ester substrate, followed by protonation to form the product and release of hydrogen fluoride. This reaction can be catalyzed by palladium-catalyzed coupling reactions with alkylthio groups.Formula:C2F3KO2Purity:Min. 95%Molecular weight:152.11 g/mol