Name | flumorph |
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Synonyms |
X5977
(EZ)-4-[3-(3,4-Dimethoxyphenyl)-3-(4-fluorophenyl)acryloyl]morpholine Flumorph [ISO] 4-[3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)-1-oxo-2-propen-1-yl]morpholine (E)-3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)-1-morpholin-4-ylprop-2-en-1-one (2Ξ)-3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)-1-(morpholin-4-yl)prop-2-en-1-one [50% (E)-isomer, 50% (Z)-isomer] (EZ)-3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)-1-morpholinopropenone [50% (E)-isomer, 50% (Z)-isomer] 3-(3,4-Dimethoxyphenyl)-3-(4-fluorophenyl)-1-morpholinoprop-2-en-1-one Flumorph 4-(3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)-1-oxo-2-propenyl)morpholine (EZ)-4-[3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)acryloyl]morpholine |
Description | Flumorph(SYP-L190) is a carboxylic acid amide (CAA) fungicide.IC50 value:Target: Fungicide agentFlumorph did not inhibit the synthesis of cell wall materials, but disturbed the polar deposition of newly synthesized cell wall materials during cystospore germination and hyphal growth. In flumorph-treated hyphae, the most characteristic change was the development of periodic swelling ("beaded" morphology) and the disruption of tip growth. Upon removing flumorph, normal tip growth and organized F-actin were observed again [1]. Flumorph had induced systemic genotoxicity in mammals as it caused DNA damage in all tested vital organs, especially in brain and spleen [2]. |
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Related Catalog | |
References |
Density | 1.208g/cm3 |
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Boiling Point | 556.3ºC at 760mmHg |
Melting Point | 122-125 °C |
Molecular Formula | C21H22FNO4 |
Molecular Weight | 371.40200 |
Flash Point | 290.3ºC |
Exact Mass | 371.15300 |
PSA | 48.00000 |
LogP | 3.07130 |
Vapour Pressure | 0mmHg at 25°C |
Index of Refraction | 1.565 |
Hazard Codes | Xn |
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RIDADR | NONH for all modes of transport |