| Identification | Back Directory | [Name]
FENAZAFLOR | [CAS]
14255-88-0 | [Synonyms]
nc5016
tarzol
lovozal
Lavozal
oms1243
ent27438
nsc191025
fenzaflor
fenozaflor
FENAZAFLOR
lavozal[qr]
oms1243[qr]
fisonsnc5016
ent27438[qr]
fenzaflor[qr]
nsc191025[qr]
fenoflurazole
Fenazaflor 0.1
fenozaflor[qr]
fenazaflor[qr]
fisonsnc5016[qr]
fenoflurazole[qr]
FEZAFLOR(FENAZAFLOR)
fenazaflor (bsi,esa,iso)
FENAZAFLOR PESTANAL, 100 MG
Fenoflurazole Solution in Acetonitrile, 1000μg/mL
5,6-dichloro-2-trifluoromethylbenzimidazole-1-carboxylate
5,6-dichloro-2-trifluoromethylbenzimidazole-1-carboxylate[qr]
5,6-DICHLORO-1-PHENOXYCARBONYL-2-TRIFLUOROMETHYLBENZIMIDAZOLE
Phenyl 5,6-dichloro-2-trifluoromethyl-1-benzimidazolecarboxylate
phenyl-5,6-dichloro-2-trifluoromethyl-benzimidazole-1-carboxylate
5,6-dichloro-1-phenoxycarbonyl-2-trifluoromethylbenzimidazole[qr]
phenyl-5,6-dichloro-2-(trifluoromethyl)-1-benzimidazolecarboxylate[qr]
phenyl-5,6-dichloro-2-trifluoromethyl-1-benzimidazole-1-carboxylate[qr]
5,6-dichloro-2-(trifluoromethyl)-1h-benzimidazole-1-carboxylicaciphenyl
5,6-dichloro-2-(trifluoromethyl)-1h-benzimidazole-1-carboxylicaciphenyle
5,6-dichloro-2-(trifluoromethyl)-1-benzimidazolecarboxylicaciphenylester
phenyl-5,6-dichloro-2-(trifluoromethyl)-1h-benzimidazole-1-carboxylate[qr]
5,6-Dichloro-2-trifluoromethyl-1H-benzimidazole-1-carboxylic acid phenyl ester
fenazaflor (ISO) phenyl 5,6-dichloro-2-trifluoromethylbenzimidazole-1-carboxylate
1H-Benzimidazole-1-carboxylic acid, 5,6-dichloro-2-(trifluoromethyl)-, phenyl ester | [EINECS(EC#)]
238-134-9 | [Molecular Formula]
C15H7Cl2F3N2O2 | [MDL Number]
MFCD00055497 | [MOL File]
14255-88-0.mol | [Molecular Weight]
375.13 |
| Hazard Information | Back Directory | [Uses]
Fenazaflor is an acaricide. | [Definition]
ChEBI: Fenazaflor is a dichlorobenzene. | [Production Methods]
Fenazaflor is commercially synthesised by esterifying 5,6-dichloro-2-(trifluoromethyl)-1H-benzimidazole-1-carboxylic acid with phenol. The production process begins with the preparation of the benzimidazole core, which is functionalized with dichloro and trifluoromethyl substituents to enhance insecticidal potency. This intermediate is then reacted with phenol or a phenol derivative under acidic or catalytic conditions to form the ester linkage, yielding the active compound. | [Mechanism of action]
Inhibits oxidative phosphorylation. Contact action. | [Pesticide Type]
Insecticide; Acaricide; Miticide |
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| Company Name: |
Energy Chemical
|
| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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