Weight | 293.548 g/mol |
---|---|
Formula | C9H10BrClN2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
CHLORBROMURON (13360-45-7)
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- Chlorbromuron urea herbicide removal by electro-Fenton reaction in aqueous effluents. (Water Research, 2009)
- Direct determination of monolinuron, linuron and chlorbromuron residues in potato samples by gas chromatography with nitrogenphosphorus detection (Journal of Chromatography A, 2003)
- Degradation of chlorbromuron and related compounds by the fungus Rhizoctonia solani. (Applied and Environmental Microbiology, 1972)
- Phototransformation of linuron and chlorbromuron in aqueous solution (Pesticide Science, 1997)
- Photodegradation of Chlorbromuron, Atrazine, and Alachlor in Aqueous Systems under Solar Irradiation (International Journal of Photoenergy, 2006)
- Soil metabolism of the herbicide chlorbromuron in rape celery crops (Soil Biology & Biochemistry, 1988)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Maloran
-
SMILESCN(C(=O)NC1=CC(=C(C=C1)Br)Cl)OC
-
InChIKeyNLYNUTMZTCLNOO-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
N,O-Dimethylhydroxylamine
(Schotten-Baumann amide from acid)
Methylboronic acid
+
Reactant
(Chan-Lam coupling reaction)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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2 alternate names
4 safety hazards
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propanil
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diuron
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chlorpropham
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(99-93-4)
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(15165-67-0)
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(94-13-3)
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m-Cumenyl methylcarbamate
(64-00-6)
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(22259-30-9)
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2,4,5-t Isobutyl ester
(4938-72-1)
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(3399-22-2, 94-60-0, 3399-21-1)
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