ChemicalBook--->CAS DataBase List--->366815-39-6

366815-39-6

366815-39-6 Structure

366815-39-6 Structure
IdentificationBack Directory
[Name]

Fenaminstrobin
[CAS]

366815-39-6
[Synonyms]

SYP1620
SYP-1620
SYP 1620
Fenaminstrobin
Fenaminostrobin
Fenaminstrobin Solution, 100ppm
Fenaminstrobin Solution, 1000ppm
Benzeneacetamide, 2-[[[(E)-[(2E)-3-(2,6-dichlorophenyl)-1-methyl-2-propen-1-ylidene]amino]oxy]methyl]-α-(methoxyimino)-N-methyl-, (αE)-
[Molecular Formula]

C21H21Cl2N3O3
[MDL Number]

MFCD32205822
[MOL File]

366815-39-6.mol
[Molecular Weight]

434.32
Chemical PropertiesBack Directory
[Melting point ]

131-133 °C(Solv: ethanol (64-17-5); ethyl acetate (141-78-6))
[density ]

1.22±0.1 g/cm3(Predicted)
[pka]

11.27±0.46(Predicted)
[Stability:]

Light Sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H335-H302-H319
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Uses]

Fenaminstrobin is used as a fungicide and pesticide.
[Definition]

ChEBI: Fenaminstrobin is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2E)-{2-[({(E)-[(3E)-4-(2,6-dichlorophenyl)but-3-en-2-ylidene]amino}oxy)methyl]phenyl}(methoxyimino)acetic acid with the amino group of methylamine. A broad-spectrum fungicide. It has a role as a mitochondrial cytochrome-bc1 complex inhibitor and an antifungal agrochemical. It is an oxime O-ether, a monocarboxylic acid amide, an olefinic compound, a dichlorobenzene, an amide fungicide and a methoxyiminoacetamide strobilurin antifungal agent.
[Production Methods]

Fenaminstrobin is produced commercially through a strobilurin-type synthetic route that constructs its methoxyiminoacetamide backbone and couples it with a dichlorophenyl-substituted butenylidene fragment. The process begins with preparation of the methoxyiminoacetic acid derivative, which is then condensed with methylamine to form the amide core. In parallel, a 2,6-dichlorophenyl butenylidene intermediate is synthesised via controlled halogenation and olefination steps. These fragments are joined through an oxy-methyl linkage to yield the characteristic strobilurin structure. Industrial production requires strict control of stereochemistry to ensure the biologically active (E,E)-configuration, followed by purification through recrystallization or chromatography to achieve technical-grade material.
[Mechanism of action]

Broad-spectrum. Respiration inhibitor- Quinone Outside Inhibitor (QoI).
[Pesticide Type]

Fungicide
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