| Weight | 198.653 g/mol |
|---|---|
| Formula | C9H11ClN2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
MONURON (150-68-5)
monouron · chlorophenyl dimethylurea
Score:
#9 in Botany
,
#529 in Biochemistry
,
#1629 in Biology
,
#1921 in Chemistry
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- Photocatalytic degradation of Monuron in aqueous titanium dioxide dispersions (Environmental Science & Technology, 1993)
- The number of sites sensitive to 3-(3,4-dichlorophenyl)-1,1-dimethylurea, 3-(4-chlorophenyl)-1,1-dimethylurea and 2-chloro-4-(2-propylamino)-6-ethylamino-s-triazine in isolated chloroplasts (Biochimica et Biophysica Acta, 1965)
- Inhibition of spinach chloroplast photosynthetic reactions by p-chlorophenyl-1,1-dimethylurea (Archives of Biochemistry and Biophysics, 1960)
- Kinetics of oxidative degradation/mineralization pathways of the phenylurea herbicides diuron, monuron and fenuron in water during application of the electro-Fenton process (Applied Catalysis B-environmental, 2010)
- Photodecomposition of 3-(p-chlorophenyl)-1,1-dimethylurea (monuron). (Journal of Agricultural and Food Chemistry, 1969)
- A highly sensitive and rapid ELISA for the arylurea herbicides diuron, monuron, and linuron (Journal of Agricultural and Food Chemistry, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - H412: Harmful to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 3 - monouron
- chlorophenyl dimethylurea
-
SMILESCN(C)C(=O)NC1=CC=C(C=C1)Cl
-
InChIKeyBMLIZLVNXIYGCK-UHFFFAOYSA-N
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Synthesis
Reactant
+
Dimethylamine
(Schotten-Baumann amide from acid)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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(94-12-2)
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(99-76-3)
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(8047-99-2, 80-39-7)
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(5471-51-2)
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(99-98-9)
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(101-10-0)
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(1918-18-9)
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(87-25-2)
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(93-55-0)
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274671-61-3
(274671-61-3)
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(93-05-0)
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(7756-96-9)
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(118-61-6, 1321-50-2)
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(101-97-3)
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(70750-03-7, 93-89-0, 70750-02-6, 70750-04-8)
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(7493-63-2)
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(80-40-0)
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(1943-79-9)
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(536-60-7)
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N-METHYLBENZAMIDE
(613-93-4)
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4-Methoxybenzyl acetate
(1331-83-5, 104-21-2)
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(150436-68-3, 4276-74-8, 13794-15-5)
3 alternate names
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(7227-91-0)
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(1322-01-6, 2052-14-4)
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(94-80-4)
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(1197-21-3)
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4 safety hazards
3 suppliers
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(1331-92-6, 78605-96-6, 122-40-7)
3 alternate names
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3 suppliers
2-TERT-BUTYLPHENOL
(88-18-6, 27178-34-3)
3 alternate names
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(1331-92-6, 101365-33-7, 122-40-7)
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(104-28-9)
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(62-75-9, 138-89-6)
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MONURON
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