| Weight | 355.7 g/mol |
|---|---|
| Formula | C12H13ClF3N3O4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
FLUCHLORALIN (33245-39-5)
Basalin · N-(2-chloroethyl)-2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline
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- Persistence and effect of butachlor and basalin on the activities of phosphate solubilizing microorganisms in wetland rice soil. (Bulletin of Environmental Contamination and Toxicology, 2002)
- Genotoxicity of the herbicide fluchloralin on human lymphocytes in vitro: chromosomal aberration and micronucleus tests. (Mutation Research\/genetic Toxicology, 1995)
- Photochemistry of bioactive compounds. Multiphase photodegradation of basalin. (Journal of Agricultural and Food Chemistry, 1974)
- Metabolism of trifluralin, profluralin, and fluchloralin by rat liver microsomes (Pesticide Biochemistry and Physiology, 1977)
- Metabolism and selectivity of fluchloralin in soybean roots. (Journal of Agricultural and Food Chemistry, 1979)
- Fluchloralin is cytotoxic and genotoxic and induces apoptosis in mammalian cells (Environmental and Molecular Mutagenesis, 1998)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Basalin
- N-(2-chloroethyl)-2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline
-
SMILESCCCN(CCCl)C1=C(C=C(C=C1[N+](=O)[O-])C(F)(F)F)[N+](=O)[O-]
-
InChIKeyMNFMIVVPXOGUMX-UHFFFAOYSA-N
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Synthesis
Propylboronic acid
+
Benzenamine, N-(2-chloroethyl)-2,6-dinitro-4-(trifluoromethyl)-
(Chan-Lam coupling reaction)
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FLUCHLORALIN
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