Weight | 242.061 g/mol |
---|---|
Formula | C10H5Cl2NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
Quinclorac (84087-01-4, 113875-40-4)
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- Effects of the herbicides clomazone, quinclorac, and metsulfuron methyl on acetylcholinesterase activity in the silver catfish (Rhamdia quelen) (Heptapteridae) (Ecotoxicology and Environmental Safety, 2005)
- Binding interaction of quinclorac with bovine serum albumin: A biophysical study (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2009)
- Resistance to acetolactate synthase inhibitors and quinclorac in a biotype of false cleavers (Galium spurium) (Weed Science, 1998)
- The mechanism of quinclorac selectivity in grasses (Pesticide Biochemistry and Physiology, 2000)
- Evidence for a Causative Role of Cyanide, Derived from Ethylene Biosynthesis, in the Herbicidal Mode of Action of Quinclorac in Barnyard Grass (Pesticide Biochemistry and Physiology, 1995)
- Mechanism of resistance to quinclorac in smooth crabgrass (Digitaria ischaemum) (Pesticide Biochemistry and Physiology, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H317: May cause an allergic skin reaction
Warning Sensitization, Skin - Category 1 -
SMILESC1=CC(=C(C2=NC=C(C=C21)Cl)C(=O)O)Cl
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InChIKeyFFSSWMQPCJRCRV-UHFFFAOYSA-N
- Pubchem - Quinclorac
- Wikipedia - quinclorac
Quinclorac is a selective herbicide used primarily to control weeds in rice crops, but is also used on other agricultural crops and is found in some household herbicides for lawn use. Most lawn maintenance companies use the product for the control of annual grass weeds like crabgrass. Quinclorac is considered a synthetic auxin.
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methyl quinoline-3-carboxylate
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