ChemicalBook--->CAS DataBase List--->50594-67-7

50594-67-7

50594-67-7 Structure

50594-67-7 Structure
IdentificationBack Directory
[Name]

ACIFLUORFEN METHYL ESTER
[CAS]

50594-67-7
[Synonyms]

MC-10108
Aciuorfen Methyl
methylacifluorfen
Acifluorfen Methyl Ester-D3
ACIFLUORFEN METHYL ESTER STANDARD
Acifluorfen Methyl Ester@100 μg/mL in MeOH
Aciuorfen methyl, 10 μg /μL in Acetonitrile
Acifluorfen Methyl Ester @1000 μg/mL in MeOH
Benzoic acid, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-, methyl ester
[Molecular Formula]

C15H9ClF3NO5
[MOL File]

50594-67-7.mol
[Molecular Weight]

375.68
Chemical PropertiesBack Directory
[Melting point ]

58-59 °C(Solv: acetone (67-64-1))
[Boiling point ]

392.3±42.0 °C(Predicted)
[density ]

1.472±0.06 g/cm3(Predicted)
[form ]

Solid-Liquid Mixture
[color ]

White to off-white
[EPA Substance Registry System]

Acifluorfen-methyl (50594-67-7)
Safety DataBack Directory
[HS Code ]

29252900
Hazard InformationBack Directory
[Uses]

Acifluorfen-methyl is an intermediate in the synthesis of Acifluorfen-methyl-2-amino (A189975), a derivative of Acifluorfen (A795248), a herbicide.
[Production Methods]

Acifluorfen-methyl is produced by first synthesising technical acifluorfen, which is formed through nitration, ether formation, and coupling steps that build the diphenyl-ether herbicide core. Once the parent acid is available, manufacturers convert it into the methyl ester to improve handling, stability and formulation flexibility. This esterification is carried out by reacting acifluorfen with methanol in the presence of an acid catalyst under controlled temperature, yielding the methyl ester through standard alcoholysis of the carboxylic acid.
[Mechanism of action]

Selective contact action being absorbed by foliage and roots. Inhibition of protoporphyrinogen oxidase (PPO) - cell membrane disruption
[Pesticide Type]

Herbicide
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