Customization: | Available |
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CAS No.: | 86763-47-5 |
Formula: | C15h22clno2 |
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Isomerism | A chiral molecule with two enantiomers - S- and R-. The technical material is an isomeric mixture but it is the R-isomer that exhibits the strongest herbicidal activity. |
Chemical formula | C15H22ClNO2 |
Canonical SMILES | CCC1=CC=CC(=C1N(COC(C)C)C(=O)CCl)C |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | KZNDFYDURHAESM-UHFFFAOYSA-N |
International Chemical Identifier (InChI) | InChI=1S/C15H22ClNO2/c1-5-13-8-6-7-12(4)15(13)17(14(18)9-16)10-19-11(2)3/h6-8,11H,5,9-10H2,1-4H3 |
Pesticide type | Herbicide |
Substance group | Chloroacetanilide |
Minimum active substance purity | 943 g/kg |
Known relevant impurities | EU dossier - none declared |
Substance origin | Synthetic |
Mode of action | Inhibits protein synthesis and so blocks cell division, selective, absorbed by shoots of germinating plants. Inhibition of VLCFA (inhibition of cell division). |
CAS RN | 86763-47-5 |
EC number | - |
CIPAC number | - |
US EPA chemical code | - |
PubChem CID | 167454 |
Molecular mass (g mol-1) | 283.80 |
PIN (Preferred Identification Name) | 2-chloro-N-(2-ethyl-6-methylphenyl)-N-[(propan-2-yloxy)methyl]acetamide |
IUPAC name | 2-chloro-6'-ethyl-N-isopropoxymethylacet-ortho-toluidide |
CAS name | 2-chloro-N-(2-ethyl-6-methylphenyl)-N-((1-methylethoxy)methyl)acetamide |
Other status information | Chemical subject to PIC regulations |
Relevant Environmental Water Quality Standards | - |
Herbicide Resistance Classification (HRAC) | K3 |
Herbicide Resistance Classification (WSSA) | 15 |