| Identification | Back Directory | [Name]
(E)-METOMINOSTROBIN | [CAS]
133408-50-1 | [Synonyms]
ssf-126
Metominofen
(E)-MetoMino
(E)-Metominost
Metominostrobin
Metominostrobin (E)
(E)-METOMINOSTROBIN
Metominostrobin [iso]
(E)-Metominostrobin PESTANAL
(E)-Metominostrobin Standard
metominostrobin (bsi, pa iso)
(E)-Metominostrobin Solution, 100ppm
(E)-Metominostrobin@100 μg/mL in Acetonitrile
(E)-Metominostrobin@1000 μg/mL in Acetonitrile
(E)-2-(MethoxyiMino)-N-Methyl-2-(2-phenoxyphenyl)acetaMide
methyl (e)-α-methoxyimino-n-methyl-2-phenoxyphenylacetamide
Benzeneacetamide, α-(methoxyimino)-N-methyl-2-phenoxy-, (αE)- | [Molecular Formula]
C16H16N2O3 | [MDL Number]
MFCD03792728 | [MOL File]
133408-50-1.mol | [Molecular Weight]
284.31 |
| Chemical Properties | Back Directory | [Melting point ]
88℃ | [density ]
1.13±0.1 g/cm3(Predicted) | [storage temp. ]
0-6°C | [pka]
11.37±0.46(Predicted) | [color ]
white crystal solid | [Henry's Law Constant]
2.5×104 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) | [Major Application]
agriculture
environmental | [InChI]
1S/C16H16N2O3/c1-17-16(19)15(18-20-2)13-10-6-7-11-14(13)21-12-8-4-3-5-9-12/h3-11H,1-2H3,(H,17,19)/b18-15+ | [InChIKey]
HIIRDDUVRXCDBN-OBGWFSINSA-N | [SMILES]
CNC(=O)C(=N\OC)\c1ccccc1Oc2ccccc2 | [Uses]
Agricultural chemical. | [CAS DataBase Reference]
133408-50-1 |
| Hazard Information | Back Directory | [Definition]
ChEBI: A monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2E)-(methoxyimino)(2-phenoxyphenyl)acetic acid with the amino group of methylamine. Used for the control of Pyricularia oryzae on rice crops. | [Hazard]
Moderately toxic by ingestion. | [Production Methods]
The industrial production of metominostrobin involves the preparation of methyl (E)-α-methoxyiminoacetic acid, which is then reacted with N-methyl-2-phenoxyphenylamine under controlled conditions to form the active compound. This condensation reaction yields the final molecule: (E)-methyl α-methoxyimino-N-methyl-2-phenoxyphenylacetamide. The synthesis is optimised for stereoselectivity to ensure the biologically active (E)-isomer predominates. | [Mechanism of action]
Systemic with broad-spectrum curative and protectant activity, inhibits respiratory electron transfer. Respiration inhibitor (QoL fungicide). | [Pesticide Type]
Fungicide |
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| Company Name: |
Energy Chemical
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| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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