| Weight | 400.519 g/mol |
|---|---|
| Formula | C23H32N2O4 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Pinoxaden (243973-20-8)
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- Prevalence of cross or multiple resistance to the acetylcoenzyme A carboxylase inhibitors fenoxaprop, clodinafop and pinoxaden in blackgrass (Alopecurus myosuroides Huds.) in France (Pest Management Science, 2009)
- Pinoxaden - for broad spectrum grass weed management in cereal crops (2006)
- Allelic variation of the ACCase gene and response to ACCase-inhibiting herbicides in pinoxaden-resistant Lolium spp. (Pest Management Science, 2011)
- Mechanism for the inhibition of the carboxyltransferase domain of acetyl-coenzyme A carboxylase by pinoxaden. (Proceedings of the National Academy of Sciences of the United States of America, 2010)
- Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part I: Discovery of the novel cereal herbicide pinoxaden (Bioorganic & Medicinal Chemistry, 2009)
- Japanese Foxtail (Alopecurus japonicus) Resistance to Fenoxaprop and Pinoxaden in China (Weed Science, 2012)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCC1=CC(=CC(=C1C2=C(N3CCOCCN3C2=O)OC(=O)C(C)(C)C)CC)C
-
InChIKeyMGOHCFMYLBAPRN-UHFFFAOYSA-N
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