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About This Item
Linear Formula:
FCH2CONH2
CAS Number:
Molecular Weight:
77.06
Beilstein:
1739054
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
form
solid
Quality Level
mp
106-108 °C (lit.)
functional group
amide
fluoro
SMILES string
NC(=O)CF
InChI
1S/C2H4FNO/c3-1-2(4)5/h1H2,(H2,4,5)
InChI key
FVTWJXMFYOXOKK-UHFFFAOYSA-N
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General description
Fluoroacetamide is a rodenticide that can be assayed by gas chromatography/mass spectrometry.
Application
Reactant involved in:
Used in mass databases for screening of pesticide residues via fast liquid chromatography TOF mass spectrometry
- C-N coupling to amides and nitrogen-containing heterocycles
- Substitution in aryl triflates
Used in mass databases for screening of pesticide residues via fast liquid chromatography TOF mass spectrometry
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 2 Oral
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Xiaowei Zhu et al.
International journal of molecular sciences, 20(11) (2019-06-13)
Cuticular wax is a mixture of very long chain fatty acids (VLCFAs) and their derivatives, which determines vital roles for plant growth. In cabbage, the cuticular wax content of leaf blades is an important trait influencing morphological features of the
U Taitelman et al.
Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement, 6, 228-231 (1983-01-01)
Two cases are reported of severe acute fluoroacetamide poisoning in man, with successful treatment of the life-threatening cardiac arrhythmias by the administration of calcium chloride. The arrhythmias were preceded by prolongation of the QT interval in the ECG. Calcium chloride
Arun K Ghosh et al.
The Journal of organic chemistry, 74(10), 3689-3697 (2009-04-14)
Synthesis and reactivity of N-methoxy-N-methyl-(1,3-benzothiazol-2-ylsulfonyl)fluoroacetamide, a building block for Julia olefination, is reported. This reagent undergoes condensation reactions with aldehydes and cyclic ketones to give alpha-fluorovinyl Weinreb amides. Olefination reactions proceed under mild, DBU-mediated conditions, or in the presence of
P J Kostyniak et al.
Toxicology letters, 22(2), 217-222 (1984-08-01)
2,4-Dinitrofluorobenzene (DNFB) reacts with glutathione to form a stable product similar to that formed with the model glutathione-S-transferase (GST) substrate, 1-chloro-2,4-dinitrobenzene (CDNB). DNFB is approx. 40 times als reactive as CDNB in this chemical reaction. The enzymatic defluorination of DNFB
Sergey V Kuznetsov et al.
Journal of applied toxicology : JAT, 27(6), 538-550 (2007-03-14)
A study was conducted of acute intoxication of infant and adult Wistar rats with fluoroacetamide (FAA), an inhibitor of oxidative metabolism. FAA was administered orally to adult rats at 1/2 LD(50) and subcutaneously to infant rats at LD(100) or 1/10
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