| Weight | 292.334 g/mol |
|---|---|
| Formula | C19H16O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
COUMATETRALYL (5836-29-3)
coumateralyl
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- Exposure of Raptors and Waterbirds to Anticoagulant Rodenticides (Difenacoum, Bromadiolone, Coumatetralyl, Coumafen, Brodifacoum): Epidemiological Survey in Loire Atlantique (France) (Bulletin of Environmental Contamination and Toxicology, 2007)
- Some rodenticidal properties of coumatetralyl (Journal of Hygiene, 1969)
- Coumarins and the vitamin K-K epoxide cycle. Lack of resistance to coumatetralyl in warfarin-resistant rats (Biochemical Pharmacology, 1976)
- X-ray structures of the anticoagulants coumatetralyl and chlorophacinone. Theoretical calculations and SAR investigations on thirteen anticoagulant rodenticides (Journal of Molecular Structure, 1999)
- Susceptibility to the anticoagulants bromadiolone and coumatetralyl in wild Norway rats (Rattus norvegicus) from the UK and Germany (International Journal of Pest Management, 2007)
- Determination of Warfarin and Coumatetralyl in Serum by HPLC Coupled with Electrospray Ionization Mass Spectrometry (Journal of Liquid Chromatography & Related Technologies, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H300: Fatal if swallowed
Danger Acute toxicity, oral - Category 1, 2 - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 - coumateralyl
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SMILESC1CC(C2=CC=CC=C2C1)C3=C(C4=CC=CC=C4OC3=O)O
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InChIKeyULSLJYXHZDTLQK-UHFFFAOYSA-N
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