| Weight | 259.103 g/mol |
|---|---|
| Formula | C9H11BrN2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
METOBROMURON (3060-89-7)
3-(p-bromophenyl)-1-methoxy-1-methylurea · Patoran
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- Photochemical versus coupled photochemical-biological flow system for the treatment of two biorecalcitrant herbicides: metobromuron and isoproturon (Applied Catalysis B-environmental, 2000)
- Phototransformation of metobromuron in the presence of TiO2 (Applied Catalysis B-environmental, 2005)
- Metobromuron: acetylation of the aniline moiety as a detoxification mechanism. (Science, 1970)
- Metabolism of 3-(p-bromophenyl)-1-methoxy-1-methylurea (metobromuron) by selected soil microorganisms. (Journal of Agricultural and Food Chemistry, 1970)
- Photolysis of 3-(p-bromophenyl)-1-methoxy-1-methylurea (Journal of Agricultural and Food Chemistry, 1968)
- Behaviour of two sunflower herbicides (metobromuron, aclonifen) in soil (European Journal of Agronomy, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-(p-bromophenyl)-1-methoxy-1-methylurea
- Patoran
-
SMILESCN(C(=O)NC1=CC=C(C=C1)Br)OC
-
InChIKeyWLFDQEVORAMCIM-UHFFFAOYSA-N
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Synthesis
Reactant
+
N,O-Dimethylhydroxylamine
(Schotten-Baumann amide from acid)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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