| Identification | Back Directory | [Name]
N-methyl-alpha-methoxy-2-[(2,5-dimethylphenoxy)methyl]phenylacetamide | [CAS]
173662-97-0 | [Synonyms]
MANDESTROBIN
Mandestrobin Standard
Benzeneacetamide, 2-[(2,5-dimethylphenoxy)methyl]-α-methoxy-N-methyl-
Benzeneacetamide, 2-[(2,5-dimethylphenoxy)methyl]-α-methoxy-N-methyl-
2-(2-((2,5-dimethylphenoxy)methyl)phenyl)-2-methoxy-N-methylacetamide
N-methyl-alpha-methoxy-2-[(2,5-dimethylphenoxy)methyl]phenylacetamide | [Molecular Formula]
C19H23NO3 | [MOL File]
173662-97-0.mol | [Molecular Weight]
313.39 |
| Hazard Information | Back Directory | [Uses]
Mandestrobin is a novel fungicide having a methoxyacetamid structure. Mandestrobin also shows safer profiles for human health and the environment. | [Definition]
ChEBI:2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of {2-[(2,5-dimethylphenoxy)methyl]phenyl}(methoxy)acetic acid with the amino group of methylamine. It is a monocarboxylic acid amide and an aromatic ether. | [Production Methods]
Mandestrobin is produced commercially through a strobilurin-type synthetic route that assembles its methoxyacrylate fungicide framework. Industrial synthesis begins with preparation of a substituted benzyl alcohol intermediate, which is functionalised via etherification to introduce the oxymethyl linkage. In parallel, a methoxyiminoacetic acid derivative is synthesised to provide the characteristic methoxyacrylate moiety. These fragments are then coupled under controlled esterification conditions to yield the final mandestrobin structure. | [Mechanism of action]
Quinone Outside Inhibitor (QoI). | [Pesticide Type]
Fungicide |
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Struchem Co., Ltd.
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http://www.beidapharma.com |
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