| Weight | 381.37 g/mol |
|---|---|
| Formula | C14H15N5O6S |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
METSULFURON-METHYL (74223-64-6)
Score:
#1925 in Biology
,
#2336 in Chemistry
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- Adsorption and degradation of chlorsulfuron and metsulfuron-methyl in soils from different depths (Weed Research, 1989)
- Effects of the herbicides clomazone, quinclorac, and metsulfuron methyl on acetylcholinesterase activity in the silver catfish (Rhamdia quelen) (Heptapteridae) (Ecotoxicology and Environmental Safety, 2005)
- Preconcentration and determination of nicosulfuron, thifensulfuron-methyl and metsulfuron-methyl in water samples using carbon nanotubes packed cartridge in combination with high performance liquid chromatography (Analytica Chimica Acta, 2006)
- Molecularly imprinted polymer for metsulfuron-methyl and its binding characteristics for sulfonylurea herbicides (Analytica Chimica Acta, 2002)
- An integrated approach to evaluate the impacts of the herbicides glyphosate, 2,4-D and metsulfuron-methyl on soil microbial communities in the Pampas region, Argentina (Applied Soil Ecology, 2008)
- The relative movement and persistence in soil of chlorsulfuron, metsulfuronmethyl and triasulfuron (Weed Research, 1989)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - 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=C2C(=O)OC
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InChIKeyRSMUVYRMZCOLBH-UHFFFAOYSA-N
- Pubchem - METSULFURON-METHYL
- Wikipedia - metsulfuron-methyl
Metsulfuron-methyl is an organic compound classified as a sulfonylurea herbicide, which kills broadleaf weeds and some annual grasses. It is a systemic compound with foliar and soil activity, that inhibits cell division in shoots and roots. It has residual activity in soils, allowing it to be used infrequently but requiring up to 22 months before planting certain crops (sunflowers, flax, corn, or safflower).
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Alternate Names
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Synthesis
Reactant
+
57683-71-3
(Schotten-Baumann amide from acid)
Methyl 2-(chlorosulfonyl)benzoate
+
Reactant
(Sulfonamide)
Similar Compounds
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METSULFURON-METHYL
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