| Weight | 527.414 g/mol |
|---|---|
| Formula | C30H23BrO4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 5 |
| Rotatable Bonds | 6 |
Bromadiolone (28772-56-7)
bromodialone
Score:
#79 in Environmental science
,
#567 in Biology
,
#603 in Chemistry
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- Fluorescence spectroscopic study of serum albumin-bromadiolone interaction: fluorimetric determination of bromadiolone. (Journal of Pharmaceutical and Biomedical Analysis, 2005)
- Field evidence of secondary poisoning of foxes (Vulpes vulpes) and buzzards (Buteo buteo) by bromadiolone, a 4-year survey (Chemosphere, 1997)
- Laboratory evaluation of bromadiolone as a rodenticide for use against warfarin-resistant and non-resistant rats and mice. (Journal of Hygiene, 1976)
- Trials of the anticoagulant rodenticides bromadiolone and difenacoum against the house mouse (Mus musculus L.). (Journal of Hygiene, 1981)
- Persistence of bromadiolone anticoagulant rodenticide in Arvicola terrestris populations after field control. (Environmental Research, 2006)
- Simultaneous determination of warfarin and bromadiolone by derivative synchronous fluorescence spectrometry. (Talanta, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - bromodialone
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SMILESC1=CC=C(C=C1)C(CC(C2=CC=C(C=C2)C3=CC=C(C=C3)Br)O)C4=C(C5=CC=CC=C5OC4=O)O
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InChIKeyOWNRRUFOJXFKCU-UHFFFAOYSA-N
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Synthesis
4-Hydroxycoumarin
+
Reactant
(Friedel-Crafts alkylation)
1,4-Dibromobenzene
+
Reactant
(Stille)
Reactant
+
1-Bromo-4-chlorobenzene
(Suzuki)
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Bromadiolone
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