Weight | 77.058 g/mol |
---|---|
Formula | C2H4FNO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
FLUOROACETAMIDE (640-19-7)
Score:
#495 in Biochemistry
,
#1566 in Biology
,
#1836 in Chemistry
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- Sigma-Aldrich - FLUOROACETAMIDE85.30 USD
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- The genetic analysis of regulation of amidase synthesis in Aspergillus nidulans. II. Mutants resistant to fluoroacetamide. (Molecular Genetics and Genomics, 1970)
- Enzymatic defluorination and metabolism of fluoroacetate, fluoroacetamide, fluoroethanol, and (-)-erythro-fluorocitrate in rats and mice examined by 19F and 13C NMR. (Chemical Research in Toxicology, 1989)
- Isolation of Bacteria able to metabolize Fluoroacetate or Fluoroacetamide (Nature, 1965)
- The enantioselective fluoroacetamide acetal Claisen rearrangements of N-fluoroacetyl-trans-(2R-5R)-2,5-dimethylpyrrolidine (Tetrahedron Letters, 1991)
- Selective destruction in testes induced by fluoroacetamide (Cellular and Molecular Life Sciences, 1964)
- Specific Effect of Fluoroacetamide on Spermiogenesis (Biology of Reproduction, 1970)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H300: Fatal if swallowed
Danger Acute toxicity, oral - Category 1, 2 - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 -
SMILESC(C(=O)N)F
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- Pubchem - FLUOROACETAMIDE
- Wikipedia - fluoroacetamide
Fluoroacetamide is an organic compound based on acetamide with one fluorine atom replacing hydrogen on the methyl group. it is a metabolic poison which disrupts the citric acid cycle and was used as a rodenticide.
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