| Weight | 419.385 g/mol |
|---|---|
| Formula | C15H16F3N5O4S |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
Prosulfuron (94125-34-5)
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- Laboratory investigations into the effects of the pesticides mancozeb, chlorothalonil, and prosulfuron on nitrous oxide and nitric oxide production in fertilized soil (Soil Biology & Biochemistry, 2005)
- Impact of an herbicide combination of bromoxynil and prosulfuron on soil microorganisms. (Current Microbiology, 2006)
- Effects of soil pH and soil water content on prosulfuron dissipation. (Journal of Agricultural and Food Chemistry, 2002)
- Syntheses of TiO2 photocatalysts by the molten salts method: Application to the photocatalytic degradation of Prosulfuron (Applied Catalysis B-environmental, 2004)
- Hydrolysis of prosulfuron at pH 5: Evidence for a resonance-stabilized triazine cleavage product (Pesticide Science, 1997)
- Losses of atrazine, metolachlor, prosulfuron and triasulfuron in subsurface drain water. I. Field results (Agronomie, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESCC1=NC(=NC(=N1)OC)NC(=O)NS(=O)(=O)C2=CC=CC=C2CCC(F)(F)F
-
InChIKeyLTUNNEGNEKBSEH-UHFFFAOYSA-N
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Synthesis
SCHEMBL13026224
+
Reactant
(Thiourea)
Reactant
+
2-Amino-4-methoxy-6-methyl-1,3,5-triazine
(Schotten-Baumann amide from acid)
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Prosulfuron
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