Name | triflumizole |
Synonyms | Triumizole Triflumizole triflumizole Triflumizole [iso] Triumizole Solution, 1000ppm (E)-1-(1-((4-Chloro-2-(trifluoromethyl)phenyl)imino)-2-propoxyethyl)-1H-imidazole 4-Chloro-N-[(E)-1-(1H-imidazol-1-yl)-2-propoxyethylidene]-2-(trifluoromethyl)aniline 4-chloro-N-[(1E)-1-(1H-imidazol-1-yl)-2-propoxyethylidene]-2-(trifluoromethyl)aniline (E)-N-[4-Chloro-2-(trifluoromethyl)phenyl]-1-(1H-imidazol-1-yl)-2-(propyloxy)ethanimine (E)-4-CHLORO-ALPHA,ALPHA,ALPHA-TRIFLUORO-N-(1-IMIDAZOL-1-YL-2-PROPOXYETHYLIDENE)-O-TOLUIDINE |
CAS | 99387-89-0 |
InChI | InChI=1/C15H15ClF3N3O/c1-2-7-23-9-14(22-6-5-20-10-22)21-13-4-3-11(16)8-12(13)15(17,18)19/h3-6,8,10H,2,7,9H2,1H3 |
Molecular Formula | C15H15ClF3N3O |
Molar Mass | 345.75 |
Water Solubility | 12.5 x 103 mg l-1(20 °C ) |
Vapor Presure | 1.86 x 10-4 Pa (25 °C ) |
pKa | 3.7 (base) |
Storage Condition | 2-8℃ |
Refractive Index | 1.533 |
UN IDs | 3077 |
Hazard Class | 9 |
Packing Group | III |
pure white crystals, tasteless. Melting point 63.5 °c, vapor pressure (25 °c) 1.4 x 10-5 Pa. Solubility at 25 ° C: xylene 639G/L, chloroform 2. 22kg/L, acetone 1.44/L, acetonitrile 1. 03kg/L, hexane 17g/L; Water solubility is 12. 5mg/L.
N-(N-propoxymethylformyl) was obtained by reacting 4-chloro-a, a, orotylamine with a-N-propoxyacetic acid in the presence of phosphorus pentachloride.-4-chloro-a,a,a--fluoromethylaniline, the resulting amide compound reacts with phosgene in the presence of triethylamine, and finally condenses with imidazole to obtain fluromazole.
broad-spectrum fungicide, sterol demethylation inhibitor. With internal absorption, protection, treatment, eradication. Mainly for cereals, vegetables, fruit trees and other crops to control powdery mildew, rust and so on. Can control wheat stripe disease, smut; Rice seedling disease, rice blast, flax leaf blight, can also control the tea tree anthracnose, peach brown rot, melon and vegetable blight, anthracnose and so on.
oral LD50>715mg/kg in male rats and 695mg/kg in female; Oral LD50 of 560mg/kg in male mice and 510mg/kg in female; intraperitoneal injection of LD50 was 895mg/kg in male rats and 710mg/kg in female; Intraperitoneal injection of LD50 was 710mg/kg in male mice and 530mg/kg in female, mouse subcutaneous injection LD50>5000mg/kg; Rat, mouse percutaneous LD50>5000mg/kg; Rat inhalation LC50>3.2mg/L; Carp LC50>1. 26mg/L( 48h), the oral LD50 of quail was 2 46% 7 mg/kg. Safe for bees. There was no irritation to rabbit skin, but mild irritation to eye mucosa. No carcinogenic, teratogenic and mutagenic effects were found in animal experiments.