Weight | 376.178 g/mol |
---|---|
Formula | C16H8Cl2FN5O |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 0 |
Aromatic Rings | 4 |
Rotatable Bonds | 2 |
Fluquinconazole (136426-54-5)
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- Sensitivity distributions and cross-resistance patterns of Mycosphaerella graminicola to fluquinconazole, prochloraz and azoxystrobin over a period of 9 years (Crop Protection, 2005)
- Removal of famoxadone, fluquinconazole and trifloxystrobin residues in red wines: Effects of clarification and filtration processes (Journal of Environmental Science and Health Part B-pesticides Food Contaminants and Agricultural Wastes, 2007)
- Fungal communities on roots of wheat and barley and effects of seed treatments containing fluquinconazole applied to control takeall (Plant Pathology, 2001)
- Sensitivity of fungi from cereal roots to fluquinconazole and their suppressiveness towards take-all on plants with or without fluquinconazole seed treatment in a controlled environment (Plant Pathology, 2000)
- Take-all and grain yields in sequences of winter wheat crops testing fluquinconazole seed treatment applied in different combinations of years (Annals of Applied Biology, 2004)
- Dissipation kinetics of fluquinconazole and pyrimethanil residues in apples intended for baby food production. (Food Chemistry, 2013)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 -
SMILESC1=CC2=C(C=C1F)C(=O)N(C(=N2)N3C=NC=N3)C4=C(C=C(C=C4)Cl)Cl
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