| Identification | More | [Name]
Fluotrimazol | [CAS]
31251-03-3 | [Synonyms]
1-[(3-TRIFLUOROPHENYL)DIPHENYLMETHYL]-1,2,4-TRIAZOLE
1-[Diphenyl[3-(trifluoromethyl)phenyl]methyl]-1H-1,2,4-triazole
FLUOTRIMAZOL
FLUOTRIMAZOLE
4-triazole,1-(alpha,alpha-diphenyl-m-(trifluoromethyl)benzyl)-1h-2
4-triazole,1-(diphenyl-(3-(trifluoromethyl)phenyl)methyl)-1h-2
b6660
persulon
persulon6660
FLUOTRIMAZOL PESTANAL, 250 MG
fluotrimazole (bsi,iso)
Bay 6683
BUE 0602
Persolon | [EINECS(EC#)]
250-534-5 | [Molecular Formula]
C22H16F3N3 | [MDL Number]
MFCD00078697 | [Molecular Weight]
379.38 | [MOL File]
31251-03-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
132°C | [Boiling point ]
485.6±55.0 °C(Predicted) | [density ]
1.21±0.1 g/cm3(Predicted) | [form ]
neat | [pka]
2.15±0.10(Predicted) | [BRN ]
8395848 | [Major Application]
agriculture
environmental | [InChI]
1S/C22H16F3N3/c23-22(24,25)20-13-7-12-19(14-20)21(28-16-26-15-27-28,17-8-3-1-4-9-17)18-10-5-2-6-11-18/h1-16H | [InChIKey]
LXMQMMSGERCRSU-UHFFFAOYSA-N | [SMILES]
FC(F)(F)c1cccc(c1)C(c2ccccc2)(c3ccccc3)n4cncn4 | [CAS DataBase Reference]
31251-03-3(CAS DataBase Reference) | [NIST Chemistry Reference]
Fluotrimazol(31251-03-3) |
| Safety Data | Back Directory | [WGK Germany ]
2 | [RTECS ]
XZ4803020 | [HS Code ]
29339900 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Aquatic Chronic 4 |
| Hazard Information | Back Directory | [Chemical Properties]
The pure product is white crystal. mp132℃, the solubility at 20℃ is: dichloromethane 40%, cyclohexanone 20%, toluene 10%, propylene glycol 5%, water 1.5mg/L. It is decomposed in 0.2mol/L sulfuric acid solution and stable in 0.1mol/L sodium hydroxide solution. | [Uses]
Fluotrimazol is a fluoride-containing azole fungicide. It is characterized by high biological activity and low toxicity, and has special effects on powdery mildews such as cucumbers, peaches, barley, and grapes. | [Definition]
ChEBI: Fluotrimazole is a triazole fungicide. | [Synthesis]
Using m-bromotrifluorotoluene as the starting material, the Grignard reagent is formed, followed by nucleophilic addition with benzophenone. Then it is hydrolyzed with ammonium chloride and reacted with 1,2,4-triazole under the protection of nitrogen to obtain Fluotrimazol. |
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