| Identification | Back Directory | [Name]
Flumorph | [CAS]
211867-47-9 | [Synonyms]
Flumorph
SYP-L190
Ccris 9057
Flumorph [iso]
Flumorph Solution
Flumorph(SYP-L190)
Flumorph Solution, 1000ppm
(EZ)-4-[3-(3,4-Dimethoxyphenyl)-3-(4-fluorophenyl)acryloyl]morpholine
3-(3,4-DiMethoxyphenyl)-3-(4-fluorophenyl)-1-Morpholinoprop-2-en-1-one
4-[3-(3,4-Dimethoxyphenyl)-3-(4-fluorophenyl)-1-oxo-2-propenyl]morpholine
Morpholine,4-[3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)-1-oxo-2-propenyl]-
2-Propen-1-one, 3-(3,4-dimethoxyphenyl)-3-(4-fluorophenyl)-1-(4-morpholinyl)- | [Molecular Formula]
C21H22FNO4 | [MOL File]
211867-47-9.mol | [Molecular Weight]
371.4 |
| Chemical Properties | Back Directory | [Melting point ]
122 - 125°C | [Boiling point ]
556.3±50.0 °C(Predicted) | [density ]
1.208 | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Chloroform (Slightly), Dichloromethane (Slightly), Ethyl Acetate (Slightly) | [form ]
neat | [pka]
-1.20±0.20(Predicted) | [color ]
Pale Yellow to Yellow | [Major Application]
agriculture
environmental | [InChI]
1S/C21H22FNO4/c1-25-19-8-5-16(13-20(19)26-2)18(15-3-6-17(22)7-4-15)14-21(24)23-9-11-27-12-10-23/h3-8,13-14H,9-12H2,1-2H3/b18-14+ | [InChIKey]
BKBSMMUEEAWFRX-NBVRZTHBSA-N | [SMILES]
COc1ccc(cc1OC)\C(=C/C(=O)N2CCOCC2)c3ccc(F)cc3 |
| Hazard Information | Back Directory | [Uses]
Flumorph can be used in analytical study of simultaneous determination of 106 pesticides in nuts by LC-?MS?/MS using freeze-?out combined with dispersive solid-?phase extraction purification. | [Definition]
ChEBI: A mixture comprising approximately equal amounts of (E)- and (Z)-fluomorph. It is used as an agrochemical fungicide for the control oomcyetes such as downey mildew on vegetables and grapes. | [Production Methods]
The industrial production of flumorph begins with the preparation of a substituted cinnamic acid intermediate, typically containing 3,4-dimethoxyphenyl and 4-fluorophenyl groups. This intermediate undergoes amide bond formation with morpholine under controlled conditions to yield the final compound. The synthesis is optimised for stereoselectivity to favour the biologically active isomers. | [Mechanism of action]
Systemic, displays protectant, curative and antisporulant activity, though to disturb the polar deposition of newly synthesized cell wall material | [storage]
Store at -20°C | [Pesticide Type]
Fungicide |
|
|