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Sigma-Aldrich

Potassium trifluoroacetate

98%

Synonym(s):

Trifluoroacetic acid potassium salt

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About This Item

Linear Formula:
CF3COOK
CAS Number:
Molecular Weight:
152.11
Beilstein:
3717603
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

mp

140-142 °C (lit.)

density

1.49 g/mL (lit.)

SMILES string

[K+].[O-]C(=O)C(F)(F)F

InChI

1S/C2HF3O2.K/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1

InChI key

CUNPJFGIODEJLQ-UHFFFAOYSA-M

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General description

Potassium trifluoroacetate is used as a versatile chemical reagent in various organic reactions. It can be employed as a source of trifluoroacetyl anion (CF3CO2-) in reactions involving nucleophilic substitution and acylation reactions.

Application

Potassium trifluoroacetate can be used as a reagent in trifluoromethylation reactions. It is used to synthesize trifluoromethyl thioethers via iron(II) chloride-catalyzed decarboxylation as well as a subsequent trifluoromethylation of organothiocyanates.

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 3

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Young H Lim et al.
ACS nano, 9(2), 1995-2008 (2015-01-27)
The development of well-defined polymeric nanoparticles (NPs) as delivery carriers for antimicrobials targeting human infectious diseases requires rational design of the polymer template, an efficient synthetic approach, and fundamental understanding of the developed NPs, e.g., drug loading/release, particle stability, and

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