| Identification | Back Directory | [Name]
Furconazole | [CAS]
112839-33-5 | [Synonyms]
Furconazole
2-(2,4-Dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-4-(2,2,2-trifluoroethoxy)tetrahydrofuran
1H-1,2,4-Triazole, 1-[[2-(2,4-dichlorophenyl)tetrahydro-5-(2,2,2-trifluoroethoxy)-2-furanyl]methyl]- | [Molecular Formula]
C15H14Cl2F3N3O2 | [MDL Number]
MFCD02661435 | [MOL File]
112839-33-5.mol | [Molecular Weight]
396.19 |
| Hazard Information | Back Directory | [Production Methods]
No publicly available industrial or patent literature describes a commercial manufacturing process for furconazole. However, its commercial synthesis would have followed the standard two part route used for this chemical class: (1) construction of a substituted aromatic or heteroaromatic alcohol or halide intermediate, and (2) nucleophilic substitution or coupling with a 1,2,4 triazole moiety under basic conditions to form the characteristic triazolyl alkyl ether or amide linkage. Industrial production would have used batch reactors, controlled halogenation or alkylation steps, and solvent based purification, mirroring the processes used for contemporary triazole fungicides such as propiconazole and triadimefon. | [Mechanism of action]
Sterol demethlyation inhibitor. Systemic with both protective and curative action | [Pesticide Type]
Fungicide |
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