Customization: | Available |
---|---|
CAS No.: | 107534-96-3 |
Formula: | C16h22cln3o |
Still deciding? Get samples of US$ 1/Piece
Request Sample
|
Suppliers with verified business licenses
Audited by an independent third-party inspection agency
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 |