132101
Sodium trifluoroacetate
98%
Synonym(s):
Trifluoroacetic acid sodium salt
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About This Item
Linear Formula:
CF3COONa
CAS Number:
Molecular Weight:
136.01
Beilstein:
3597949
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.22
grade:
for analytical purposes
form:
powder
Recommended Products
grade
for analytical purposes
Quality Level
Assay
98%
form
powder
mp
205-207 °C (dec.) (lit.)
density
1.49 g/mL (lit.)
functional group
fluoro
SMILES string
[Na+].[O-]C(=O)C(F)(F)F
InChI
1S/C2HF3O2.Na/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1
InChI key
UYCAUPASBSROMS-UHFFFAOYSA-M
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General description
Sodium trifluoroacetate is a trifluoromethylating agent for compounds like aromatic halides, aldehydes and ketones.
Application
Sodium trifluoroacetate can be used:
- As a trifluoromethylating agent in nucleophilic trifluoromethylation of aldehydes using copper(I) halide catalyst.
- As a difluorocarbene precursor in gem-difluorocyclopropanation of different alkenes using azobisisobutyronitrile (AIBN) as a catalyst.
- In the synthesis of trifluoromethylthio-substituted aromatic compounds via copper-mediated oxidative trifluoromethylthiolation of aryl boronic acids in the presence of elemental sulfur.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Sodium trifluoroacetate: an efficient difluorocarbene precursor for alkenes
Chang Y and Cai C
Chemistry Letters (Jpn), 34(10), 1440-1441 (2005)
Sodium trifluoroacetate: an efficient precursor for the trifluoromethylation of aldehydes
Chang Y and Cai C
Tetrahedron Letters, 46(18), 3161-3164 (2005)
Michelle Piotrowski et al.
Journal of the American Society for Mass Spectrometry, 30(3), 489-500 (2018-12-16)
A method is developed to determine the position of ion formation along the flight axis of a MALDI TOFMS instrument using the image of the laser on the sample surface. Previous work (JASMS 2018, 29, 422-434) showed that misalignment of
Copper-mediated oxidative trifluoromethylthiolation of aryl boronic acids with CF3CO2Na and elemental sulfur
Zhai L et al.
Tetrahedron, 69(48), 10262-10266 (2013)
Ruichan Lv et al.
Scientific reports, 7(1), 15753-15753 (2017-11-18)
We report here the design and multiple functions of a new hierarchical nanotheronostic platform consisting of an upconversion nanoparticle (UCNP) core: shell with an additional mesoporous silica (mSiO
Global Trade Item Number
SKU | GTIN |
---|---|
132101-25G | 4061838728821 |
132101-100G | 4061838728814 |
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