Customization: | Available |
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CAS No.: | 43121-43-3 |
Formula: | C14h16cln3o2 |
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Isomerism | A chiral molecule with one chiral centre. There is little notable difference in the biological activities of the different enantiomeric forms |
Chemical formula | C14H16ClN3O2 |
Canonical SMILES | CC(C)(C)C(=O)C(N1C=NC=N1)OC2=CC=C(C=C2)Cl |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | WURBVZBTWMNKQT-UHFFFAOYSA-N |
International Chemical Identifier (InChI) | InChI=1S/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3 |
Pesticide type | Fungicide, Metabolite |
Metabolite Type | Soil |
Substance group | Triazole |
Minimum active substance purity | - |
Known relevant impurities | - |
Substance origin | Synthetic |
Mode of action | Systemic with protective, curative and eradicant action. Disrupts membrane function. Sterol biosynthesis inhibitor. |
CAS RN | 43121-43-3 |
EC number | 256-103-8 |
CIPAC number | 352 |
US EPA chemical code | 109901 |
PubChem CID | 39385 |
Molecular mass (g mol-1) | 293.8 |
PIN (Preferred Identification Name) | rac-(1R)-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one |
IUPAC name | (RS)-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one |
CAS name | 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanone |