Weight | 131.053 g/mol |
---|---|
Formula | C2H4F3NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Ammonium trifluoroacetate (3336-58-1)
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- New applications of the Mannich reaction. Use of dimethyl(methylene)ammonium trifluoroacetate for regiospecific carbanion quenching. A new route to .alpha.-methylene-.gamma.-butyrolactone (Journal of the American Chemical Society, 1977)
- 4,4-Dimethyl-4-silapentane-1-ammonium trifluoroacetate (DSA), a promising universal internal standard for NMR-based metabolic profiling studies of biofluids, including blood plasma and serum (Metabolomics, 2008)
- Electron Spin Resonance of an Irradiated Single Crystal of Ammonium Trifluoroacetate (Journal of Chemical Physics, 1967)
- Onium ions. XVI. Hydrogen--deuterium exchange accompanying the cleavage of ammonium (tetradeuterioammonium) trifluoroacetate by lithium deuteride (hydride) indicating Sn2 like nucleophilic displacement at quaternary nitrogen through pentacoordinated NH$sub 5$ (Journal of the American Chemical Society, 1975)
- Onium ions. XVI. Hydrogen-deuterium exchange accompanying the cleavage of ammonium (tetradeuterioammonium) trifluoroacetate by lithium deuteride (hydride) indicating SN2 like nucleophilic displacement at quaternary nitrogen through pentacoordinated ammonium hydride (Journal of the American Chemical Society, 1975)
- Applications of ammonium trifluoroacetate as an additive for elution of chiral acids and bases from derivatized polysaccharide stationary phases. (Chirality, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=O)(C(F)(F)F)[O-].[NH4+]
-
InChIKeyYCNIBOIOWCTRCL-UHFFFAOYSA-N
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