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1065124-65-3

1065124-65-3 Structure

1065124-65-3 Structure
IdentificationBack Directory
[Name]

epsilon-momfluorothrin
[CAS]

1065124-65-3
[Synonyms]

ε-momfluorothrin
epsilon-momfluorothrin
Momfluorothrin, (Z,1R,3R)-
4-methoxymethyl-2,3,5,6-tetrafluorobenzyl (1R)-trans-3-((Z)-2-cyano-1-propenyl)-2,2-dimethylcyclopropane carboxylate
Cyclopropanecarboxylic acid, 3-[(1Z)-2-cyano-1-propen-1-yl]-2,2-dimethyl-, [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl ester, (1R,3R)-
[Molecular Formula]

C19H19F4NO3
[MDL Number]

MFCD32062669
[MOL File]

1065124-65-3.mol
[Molecular Weight]

385.35
Chemical PropertiesBack Directory
[Boiling point ]

403.0±45.0 °C(Predicted)
[density ]

1.321±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 5 mg/mL (12.98 mM)
[form ]

Solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
GHS07,GHS08,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302-H371-H410
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P260-P264-P270-P309+P311-P405-P501-P273-P391-P501
Hazard InformationBack Directory
[Uses]

Epsilon-momfluorothrin is a type I synthetic pyrethroid insecticide, activates constitutive androstane receptor (CAR), and induces hepatocellular tumors in rats[1].
[Definition]

ChEBI: Epsilon-momfluorothrin is a carboxylic ester obtained by formal condensation between the carboxy group of (1R,3R)-3-[(1Z)-2-cyanoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylic acid with the benzylic hydroxy group of [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methanol. It has a role as a pyrethroid ester insecticide and an agrochemical. It is a carboxylic ester, a member of cyclopropanes, an ether, an organofluorine insecticide, a tetrafluorobenzene and a nitrile. It is functionally related to a chrysanthemic acid.
[Production Methods]

Epsilon-momfluorothrin is synthesised commercially through a multi-step chemical process involving the esterification of a cyclopropane carboxylic acid derivative with a fluorinated benzyl alcohol
[Mechanism of action]

Axonic poison; keeps sodium channels in the neuronal membranes open, leading to hyperexcitation and paralysis.
[References]

[1] Okuda Y, et al. Editor's Highlight: Mode of Action Analysis for Rat Hepatocellular Tumors Produced by the Synthetic Pyrethroid Momfluorothrin: Evidence for Activation of the Constitutive Androstane Receptor and Mitogenicity in Rat Hepatocytes. Toxicol Sci. 2017 Aug 1;158(2):412-430. DOI:10.1093/toxsci/kfx102
[Pesticide Type]

Insecticide
Spectrum DetailBack Directory
[Spectrum Detail]

epsilon-momfluorothrin(1065124-65-3)1HNMR
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