Isomerism | A chiral molecule existing in the R- and S-forms, the R-isomer is considered to be the most biologically active. |
Chemical formula | C 1 5 H 1 9 N 3 O 3 |
Canonical SMILES | CCC1=CN=C(C(=C1)C(=O)O)C2=NC(C(=O)N2)(C)C(C)C |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | XVOKUMIPKHGGTN-UHFFFAOYSA-N |
International Chemical Identifier (InChI) | InChI=1S/C15H19N3O3/c1-5-9-6-10(13(19)20)11(16-7-9)12-17-14(21)15(4,18-12)8(2)3/h6-8H,5H2,1-4H3,(H,19,20)(H,17,18,21) |
Pesticide type | Herbicide |
Substance group | Imidazolinone |
Minimum active substance purity | - |
Known relevant impurities | - |
Substance origin | Synthetic |
Mode of action | Systemic with contact and residual activity. Inhibits plant amino acid synthesis - acetohydroxyacid synthase AHAS. |
CAS RN | 81335-77-5 |
EC number | - |
CIPAC number | 700 |
US EPA chemical code | 128922 |
PubChem CID | 54740 |
Molecular mass (g mol -1 ) | 289.33 |
PIN (Preferred Identification Name) | - |
IUPAC name | 5-ethyl-2-[( R S )-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]nicotinic acid |
CAS name | 2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1 H -imidazol-2-yl)-5-ethyl-3-pyridinecarboxylic acid |