CAS 918162-02-4
:Fenoxystrobin
Description:
Fenoxystrobin is a broad-spectrum fungicide belonging to the strobilurin class of compounds, which are derived from natural sources. It is primarily used in agriculture to control a variety of fungal diseases in crops, including cereals, fruits, and vegetables. The chemical structure of fenoxystrobin features a methoxyimino group, which contributes to its mode of action by inhibiting mitochondrial respiration in fungi, effectively disrupting their energy production. This compound is characterized by its systemic properties, allowing it to be absorbed and translocated within plants, providing protective and curative effects against pathogens. Fenoxystrobin is known for its low toxicity to mammals and beneficial organisms when used according to recommended guidelines. Additionally, it has a relatively low environmental persistence, making it a preferred choice in integrated pest management strategies. However, like all pesticides, it should be used with caution to minimize potential resistance development in target pathogens and to protect non-target species.
Formula:C19H16ClF3O4
InChI:InChI=1S/C19H16ClF3O4/c1-25-11-15(18(24)26-2)14-6-4-3-5-12(14)10-27-17-8-7-13(9-16(17)20)19(21,22)23/h3-9,11H,10H2,1-2H3
InChI key:InChIKey=MBHXIQDIVCJZTD-UHFFFAOYSA-N
SMILES:C(C(OC)=O)(=COC)C1=C(COC2=C(Cl)C=C(C(F)(F)F)C=C2)C=CC=C1
Synonyms:- SYP 3759
- Fujunmanzhi
- Benzeneacetic acid, 2-[[2-chloro-4-(trifluoromethyl)phenoxy]methyl]-α-(methoxymethylene)-, methyl ester
- Fenoxystrobin
- Flufenoxystrobin
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Flufenoxystrobin
CAS:Controlled Product<p>Applications Flufenoxystrobin is used as a pesticide.<br>References Yang, J., et al.: Xiandai Nongyao, 14, 1 (2015), Yang, Y., et al.: Nongyao, 50, 223 (2011)<br></p>Formula:C19H16ClF3O4Color and Shape:NeatMolecular weight:400.78Flufenoxystrobin
CAS:<p>Flufenoxystrobin is a synthetic fungicide, which is derived from the strobilurin class of compounds known for their antifungal properties. It operates by inhibiting mitochondrial respiration in fungal cells, specifically blocking the electron transport chain at the Qo site of cytochrome b. This disruption in energy production is lethal to the targeted fungi.</p>Formula:C19H16ClF3O4Purity:Min. 95%Molecular weight:400.8 g/mol


