Weight | 328.202 g/mol |
---|---|
Formula | C13H7F3N2O5 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
Fluorodifen (15457-05-3)
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- Sigma-Aldrich - Fluorodifen18.30 USD
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- Metabolism of substituted diphenylether herbicides in plants. I. Enzymatic cleavage of fluorodifen in peas (Pisum sativum L.) (Pesticide Biochemistry and Physiology, 1973)
- Crystallographic and functional characterization of the fluorodifen-inducible glutathione transferase from Glycine max reveals an active site topography suited for diphenylether herbicides and a novel L-site. (Journal of Molecular Biology, 2009)
- Mercapturic acid formation in the metabolism of propachlor, CDAA, and fluorodifen in the rat (Pesticide Biochemistry and Physiology, 1975)
- Metabolism of substituted diphenylether herbicides in plants. II. Identification of a new fluorodifen metabolite, S-(2-nitro-4-trifluoromethylphenyl)-glutathione in peanut (Pesticide Biochemistry and Physiology, 1973)
- Glutathione S-transferases of italian ryegrass (Lolium multiflorum): activity toward some chemicals, safener modulation and persistence of atrazine and fluorodifen in the shoots. (Journal of Agricultural and Food Chemistry, 2011)
- Tobacco plants over-expressing the sweet orange tau glutathione transferases (CsGSTUs) acquire tolerance to the diphenyl ether herbicide fluorodifen and to salt and drought stresses. (Phytochemistry, 2015)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1[N+](=O)[O-])OC2=C(C=C(C=C2)C(F)(F)F)[N+](=O)[O-]
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InChIKeyHHMCAJWVGYGUEF-UHFFFAOYSA-N
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