| Weight | 357.779 g/mol |
|---|---|
| Formula | C12H12ClN5O4S |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
CHLORSULFURON (112143-77-8, 64902-72-3)
chlorsulfuron, monoammonium salt
Score:
#1624 in Biology
,
#1913 in Chemistry
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- Site of Action of Chlorsulfuron: Inhibition of Valine and Isoleucine Biosynthesis in Plants (Plant Physiology, 1984)
- Metabolism of chlorsulfuron by plants: Biological basis for selectivity of a new herbicide for cereals (Pesticide Biochemistry and Physiology, 1982)
- Cross-Resistance to Herbicides in Annual Ryegrass (Lolium rigidum) : II. Chlorsulfuron Resistance Involves a Wheat-Like Detoxification System (Plant Physiology, 1991)
- Adsorption and degradation of chlorsulfuron and metsulfuron-methyl in soils from different depths (Weed Research, 1989)
- Diverse Mutations in the Acetolactate Synthase Gene Confer Chlorsulfuron Resistance in Kochia (Kochia scoparia) Biotypes1 (Weed Science, 1995)
- The relative movement and persistence in soil of chlorsulfuron, metsulfuronmethyl and triasulfuron (Weed Research, 1989)
-
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 - chlorsulfuron, monoammonium salt
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SMILESCC1=NC(=NC(=N1)OC)NC(=O)NS(=O)(=O)C2=CC=CC=C2Cl
-
InChIKeyVJYIFXVZLXQVHO-UHFFFAOYSA-N
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Synthesis
2-Chlorobenzenesulfonyl chloride
+
Reactant
(Sulfonamide)
Reactant
+
2-Amino-4-methoxy-6-methyl-1,3,5-triazine
(Schotten-Baumann amide from acid)
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CHLORSULFURON
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