| Weight | 343.213 g/mol |
|---|---|
| Formula | C18H12Cl2N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
Boscalid (188425-85-6)
Score:
#2 in Botany
,
#1041 in Biology
,
#1162 in Chemistry
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- Activity of Boscalid, Fenhexamid, Fluazinam, Fludioxonil, and Vinclozolin on Growth of Sclerotinia minor and S. sclerotiorum and Development of Lettuce Drop (Plant Disease, 2004)
- Resistance to Boscalid Fungicide in Alternaria alternata Isolates from Pistachio in California (Plant Disease, 2007)
- Characterization of Mutations in the Iron-Sulphur Subunit of Succinate Dehydrogenase Correlating with Boscalid Resistance in Alternaria alternata from California Pistachio (Phytopathology, 2008)
- Occurrence of boscalid and other selected fungicides in surface water and groundwater in three targeted use areas in the United States (Chemosphere, 2012)
- Toward a Continuous-Flow Synthesis of Boscalid (Advanced Synthesis & Catalysis, 2010)
- Sensitivity of Botrytis cinerea from vegetable greenhouses to boscalid (Plant Pathology, 2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C(=C1)C2=CC=C(C=C2)Cl)NC(=O)C3=C(N=CC=C3)Cl
-
InChIKeyWYEMLYFITZORAB-UHFFFAOYSA-N
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