ChemicalBook--->CAS DataBase List--->77501-60-1

77501-60-1

77501-60-1 Structure

77501-60-1 Structure
IdentificationMore
[Name]

Benzofluorfen
[CAS]

77501-60-1
[Synonyms]

BENZOFLUORFEN
carboxymethyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate
COMPETE
Ethoxy-2-oxoethyl (5-2-chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoate
ethoxycarbonylmethyl-5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate
FLUOROGLYCOFEN-ETHYL
Fluoroglycofen ethyl ester
Super Blazer[R]
Benzoic acid, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-, carboxymethyl ester
[Molecular Formula]

C18H13ClF3NO7
[MDL Number]

MFCD01632760
[Molecular Weight]

447.75
[MOL File]

77501-60-1.mol
Chemical PropertiesBack Directory
[Boiling point ]

517.8±50.0 °C(Predicted)
[density ]

1.575±0.06 g/cm3(Predicted)
[pka]

2.60±0.10(Predicted)
[CAS DataBase Reference]

77501-60-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Dimethyl sulfoxide
[Preparation Products]

Fluoroglycofen-ethyl E.C.
Hazard InformationBack Directory
[Description]

Fluoroglycofen is a nitrophenyl ether compound normally used as the ethyl ester. Data for the acid is scant. It is moderately toxic to mammals via the oral route.
[Uses]

Fluoroglycofen is a herbicide used in vineyards to eradicate weeds[1].
[Definition]

ChEBI: Fluoroglycofen is a nitrobenzoic acid.
[Production Methods]

Fluoroglycofen is produced commercially as the ethyl ester and involves a carefully controlled chemical synthesis process. It begins by mixing acifluorfen, toluene, and a catalyst, then heating the mixture to initiate the reaction. Potassium carbonate is added next, and the temperature is raised to promote further chemical transformation. Ethyl chloroacetate is then introduced, and the mixture is heated to 90–105 DegC to complete the esterification reaction. Once the reaction concludes, the mixture is slowly cooled and extracted using a toluene-water solution to isolate the organic layer. This layer is then distilled to remove any remaining solvents or impurities, yielding high-purity fluoroglycofen-ethyl.
[Mechanism of action]

Induces the accumulation of tetrapyroles which attack plant cells. Inhibition of protoporphyrinogen oxidase (PPO) - cell membrane disruption
[References]

[1] WeiTan, et al. Photosynthesis and growth responses of grapevine to acetochlor and fluoroglycofen. Pesticide Biochemistry and Physiology. Volume 103, Issue 3, July 2012, Pages 210-218.
[Pesticide Type]

Herbicide
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