Weight | 248.188 g/mol |
---|---|
Formula | C12H6F2N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
Fludioxonil (131341-86-1)
Score:
#126 in Microbiology
,
#394 in Biochemistry
,
#1357 in Biology
,
#1585 in Chemistry
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- Characterization of mutations in the two-component histidine kinase gene that confer fludioxonil resistance and osmotic sensitivity in the os-1 mutants of Neurospora crassa (Pest Management Science, 2001)
- Determination of photosynthetic and enzymatic biomarkers sensitivity used to evaluate toxic effects of copper and fludioxonil in alga Scenedesmus obliquus. (Aquatic Toxicology, 2005)
- Solid-phase microextraction-gas chromatographic-mass spectrometric method for the determination of the fungicides cyprodinil and fludioxonil in white wines. (Journal of Chromatography A, 2002)
- Calcineurin, Mpk1 and Hog1 MAPK pathways independently control fludioxonil antifungal sensitivity in Cryptococcus neoformans (Microbiology, 2006)
- Activity of Boscalid, Fenhexamid, Fluazinam, Fludioxonil, and Vinclozolin on Growth of Sclerotinia minor and S. sclerotiorum and Development of Lettuce Drop (Plant Disease, 2004)
- Comparative Efficacy of the New Postharvest Fungicides Azoxystrobin, Fludioxonil, and Pyrimethanil for Managing Citrus Green Mold (Plant Disease, 2007)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C2C(=C1)OC(O2)(F)F)C3=CNC=C3C#N
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InChIKeyMUJOIMFVNIBMKC-UHFFFAOYSA-N
- Pubchem - Fludioxonil
- Wikipedia - fludioxonil
Fludioxonil is a non-systemic fungicide, introduced in 1993 by Ciba-Geigy (now Syngenta). It is used for the treatment crops (particularly cereals, fruits and vegetables, and oramental plants; often in combination with another fungicide such as cyprodinil). Brand names from Syngenta include Celest (seed treatment) and Switch (fludioxonil + cyprodinil for spraying on crops).
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