| Weight | 461.776 g/mol |
|---|---|
| Formula | C19H15ClF3NO7 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 7 |
LACTOFEN (77501-63-4)
Score:
#1956 in Biology
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- Suppression of Sclerotinia stem rot of soybean by lactofen herbicide treatment (Phytopathology, 1999)
- The Diphenylether Herbicide Lactofen Induces Cell Death and Expression of Defense-Related Genes in Soybean (Plant Physiology, 2005)
- Influence of Soil Properties on the Enantioselective Dissipation of the Herbicide Lactofen in Soils (Journal of Agricultural and Food Chemistry, 2009)
- Enantioselective Degradation in Sediment and Aquatic Toxicity to Daphnia magna of the Herbicide Lactofen Enantiomers (Journal of Agricultural and Food Chemistry, 2010)
- Lactofen induces isoflavone accumulation and glyceollin elicitation competency in soybean (Phytochemistry, 2003)
- Induction of hepatic peroxisome proliferation in mice by lactofen, a diphenyl ether herbicide (Toxicology and Applied Pharmacology, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)C(C)OC(=O)C1=C(C=CC(=C1)OC2=C(C=C(C=C2)C(F)(F)F)Cl)[N+](=O)[O-]
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InChIKeyCONWAEURSVPLRM-UHFFFAOYSA-N
- Pubchem - LACTOFEN
- Wikipedia - lactofen
Lactofen is a complex ester of acifluorfen and is a nitrophenyl ether selective herbicide. It is used in postemergence applications to certain crops which are resistant to its action. The name "Lactofen" is approved by the American National Standards Institute and the Weed Science Society of America, and is also approved in China ().
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