CAS 150-68-5: 3-(4-Chlorophenyl)-1,1-dimethylurea
Formula:C9H11ClN2O
InChI:InChI=1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)
InChI key:InChIKey=BMLIZLVNXIYGCK-UHFFFAOYSA-N
SMILES:N(C(N(C)C)=O)C1=CC=C(Cl)C=C1
Synonyms:- 1,1-Dimethyl-3-(4-chlorophenyl)urea
- 1,1-Dimethyl-3-(p-chlorophenyl)urea
- 1-(4-Chloro phenyl)-3,3-dimethyluree
- 1-(4-Chlorophenyl)-3,3-Dimethyluree
- 1-(4-Chlorophenyl)-3,3-Dimethyluree(French)
- 1-(4-Chlorophenyl)-3,3-dimethylurea
- 1-(p-Chlorophenyl)-3,3-dimethylurea
- 3-(4-Chlorophenyl)-1,1-dimethylurea
- 3-(p-Chlorophenyl)-1,1-dimethylurea
- CMU
- Chlorfenidim
- See more synonyms
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Found 11 products.
Monuron 10 µg/mL in Acetonitrile
CAS:Formula:C9H11ClN2OColor and Shape:Single SolutionMolecular weight:198.65LC PestiMix 1 10 µg/mL in Acetonitrile
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Color and Shape:MixtureMonuron
CAS:Monuron is an herbicide that is used to control weeds in crops, pastures, and other agricultural settings. It inhibits cell division by binding to the dinucleotide phosphate (DNP) site on the enzyme ribonucleotide reductase. Monuron inhibits the conversion of DNP and DAP into ribonucleotides, which are necessary for DNA synthesis. Monuron has been shown to be carcinogenic in rats and mice in several studies. This may be due to its ability to inhibit DNA synthesis by preventing the uptake of amino acids into cells, which prevents protein synthesis and cell division. The mechanism of action of Monuron is similar to that of other plant growth regulators such as 2,4-Dichlorophenoxyacetic acid which also causes cancerous changes in cells.END>Formula:C9H11ClN2OPurity:Min. 95%Color and Shape:White/Off-White SolidMolecular weight:198.65 g/mol3-(4-Chlorophenyl)-1,1-dimethylurea
CAS:Formula:C9H11ClN2OPurity:>95.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:198.65Monuron 100 µg/mL in Acetonitrile
CAS:Controlled ProductFormula:C9H11ClN2OColor and Shape:Single SolutionMolecular weight:198.65
