| Identification | Back Directory | [Name]
fluromidine | [CAS]
13577-71-4 | [Synonyms]
NC-4780
fluromidine
Fluoromidine
6-Chloro-2-trifluoromethyl-1H-imidazo[4,5-b]pyridine
6-Chloro-2-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine
3H-Imidazo[4,5-b]pyridine, 6-chloro-2-(trifluoromethyl)- | [Molecular Formula]
C7H3ClF3N3 | [MDL Number]
MFCD00223328 | [MOL File]
13577-71-4.mol | [Molecular Weight]
221.57 |
| Chemical Properties | Back Directory | [Melting point ]
293 °C(Solv: ethanol (64-17-5)) | [Boiling point ]
168.7±50.0 °C(Predicted) | [density ]
1.76±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C(protect from light) | [pka]
2.35±0.20(Predicted) | [Appearance]
Light brown to gray Solid | [EPA Substance Registry System]
Fluromidine (13577-71-4) |
| Hazard Information | Back Directory | [Definition]
ChEBI: Fluoromidine is an imidazopyridine. | [Production Methods]
Commercial production information on fluoromidine is limited in open literature. However, its production can be inferred from its structure and would probably have been produced through a multi step heterocyclic synthesis in which a chlorinated pyridine precursor is condensed with an imidazole forming reagent, followed by introduction of the trifluoromethyl group using a fluorinated intermediate, an approach consistent with broader fluorinated pesticide manufacturing practices. Commercial production generally involved controlled halogenation, cyclisation to form the fused imidazopyridine ring system, and purification steps to meet technical grade specifications before formulation into herbicidal products. | [Mechanism of action]
Uncoupler of the oxidative phosphorylation process | [Pesticide Type]
Herbicide |
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Cochemical Co. Ltd.
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