Weight | 302.201 g/mol |
---|---|
Formula | C14H17Cl2NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
Fenhexamid (126833-17-8)
Score:
#5 in Botany
,
#121 in Microbiology
,
#1292 in Biology
,
#1499 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)
- Genetic Analysis of Fenhexamid-Resistant Field Isolates of the Phytopathogenic Fungus Botrytis cinerea (Antimicrobial Agents and Chemotherapy, 2008)
- The hydroxyanilide fenhexamid, a new sterol biosynthesis inhibitor fungicide efficient against the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea) (Pest Management Science, 2001)
- Rapid gas chromatographic method for the determination of famoxadone, trifloxystrobin and fenhexamid residues in tomato, grape and wine samples (Journal of Chromatography A, 2007)
- Postharvest Decay Management for Stone Fruit Crops in California Using the "Reduced-Risk" Fungicides Fludioxonil and Fenhexamid (Plant Disease, 2007)
- Metallothionein induction, antioxidative responses, glycogen and growth changes in Tubifex tubifex (Oligochaete) exposed to the fungicide, fenhexamid. (Environmental Pollution, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 - H411: Toxic to aquatic life with long lasting effects
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SMILESCC1(CCCCC1)C(=O)NC2=C(C(=C(C=C2)O)Cl)Cl
-
InChIKeyVDLGAVXLJYLFDH-UHFFFAOYSA-N
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