Customization: | Available |
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CAS No.: | 107534-96-3 |
Formula: | C9h10cln5o2 |
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Isomerism | Isomeric - existing as both the E- and Z- forms however many commerical products are comprised of almost entirely the (E)-isomer |
Chemical formula | C9H10ClN5O2 |
Canonical SMILES | C1CN(C(=N1)N[N+](=O)[O-])CC2=CN=C(C=C2)Cl |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | YWTYJOPNNQFBPC-UHFFFAOYSA-N |
International Chemical Identifier (InChI) | InChI=1S/C9H10ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-2,5H,3-4,6H2,(H,11,13) |
Pesticide type | Insecticide, Veterinary substance |
Substance group | Neonicotinoid |
Minimum active substance purity | 970 g/kg |
Known relevant impurities | EU dossier - None declared |
Substance origin | Synthetic |
Mode of action | Systemic with contact and stomach action. Acetylcholine receptor (nAChR) agonist. |
CAS RN | 138261-41-3 |
EC number | - |
CIPAC number | 582 |
US EPA chemical code | 129099 |
PubChem CID | 86418 |
Molecular mass (g mol-1) | 255.66 |
PIN (Preferred Identification Name) | - |
IUPAC name | (E)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine |
CAS name | (2E)-1-((6-chloro-3-pyridinyl)methyl)-N-nitro-2-imidazolidinimine |
Other status information | NOTE ban or usage restriction may be in place for use on flowering crops in some Member States |
Isomerism | A chiral molecule. The technical material is an isomeric mixture of the (S-) and (R-) isomers. The R-form is more biologically active than the S-form. |
Chemical formula | C16H22ClN3O |
Canonical SMILES | CC(C)(C)C(CCC1=CC=C(C=C1)Cl)(CN2C=NC=N2)O |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | PXMNMQRDXWABCY-UHFFFAOYSA-N |
International Chemical Identifier (InChI) | InChI=1S/C16H22ClN3O/c1-15(2,3)16(21,10-20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7,11-12,21H,8-10H2,1-3H3 |
Pesticide type | Fungicide, Plant growth regulator |
Substance group | Triazole |
Minimum active substance purity | 950 g/kg |
Known relevant impurities | EU dossier - None declared |
Substance origin | Synthetic |
Mode of action | Systemic with protective, curative and eradicant action. Disrupts membrane function. Sterol biosynthesis inhibitor. |
CAS RN | 107534-96-3 |
EC number | 403-640-2 |
CIPAC number | 494 |
US EPA chemical code | 128997 |
PubChem CID | 86102 |
Molecular mass (g mol-1) | 307.82 |
PIN (Preferred Identification Name) | rac-(3R)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol |
IUPAC name | (RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol |
CAS name | α-(2-(4-chlorophenyl)ethyl)-α-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol |