Famoxadone

Famoxadone
Names
IUPAC name
(RS)-5-Methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione
Other names
Famoxate; FMX
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.114.714 Edit this at Wikidata
UNII
  • InChI=1S/C22H18N2O4/c1-22(16-12-14-19(15-13-16)27-18-10-6-3-7-11-18)20(25)24(21(26)28-22)23-17-8-4-2-5-9-17/h2-15,23H,1H3 checkY
    Key: PCCSBWNGDMYFCW-UHFFFAOYSA-N checkY
  • InChI=1/C22H18N2O4/c1-22(16-12-14-19(15-13-16)27-18-10-6-3-7-11-18)20(25)24(21(26)28-22)23-17-8-4-2-5-9-17/h2-15,23H,1H3
    Key: PCCSBWNGDMYFCW-UHFFFAOYAG
  • O=C2OC(C(=O)N2Nc1ccccc1)(c4ccc(Oc3ccccc3)cc4)C
Properties
C22H18N2O4
Molar mass 374.396 g·mol−1
Melting point 140.3-141.8 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Famoxadone is a fungicide to protect agricultural products against various fungal diseases on fruiting vegetables, tomatoes, potatoes, curcurbits, lettuce and grapes.[1] It is used in combination with cymoxanil.[1][2] Famoxadone is a QoI, albeit with a chemistry different from most QoIs. (It is an oxazolidine-dione while most are strobilurins.)[3][4][5] It is commonly used against Plasmopara viticola,[3] Alternaria solani,[3][4] Phytophthora infestans,[3][4] and Septoria nodorum.[3][4]

  1. ^ a b Famoxadone Pesticide Fact Sheet, United States Environmental Protection Agency
  2. ^ Phillip Brannen. "Fungicide resistance management for powdery and downy mildews" (PDF).
  3. ^ a b c d e Knight, S. C.; Anthony, V. M.; Brady, A. M.; Greenland, A. J.; Heaney, S. P.; Murray, D. C.; Powell, K. A.; Schulz, M. A.; Spinks, C. A.; Worthington, P. A.; Youle, D. (1997). "Rationale and Perspectives on the Development of Fungicides". Annual Review of Phytopathology. 35 (1). Annual Reviews: 349–372. doi:10.1146/annurev.phyto.35.1.349. ISSN 0066-4286.
  4. ^ a b c d Schepers, Huub T. A. M.; Cooke, Louise R. (2015). "Potato Pathogens in Northern and Western Europe". In Ishii H., Hollomon D. (ed.). Fungicide Resistance in Plant Pathogens. Tokyo: Springer Japan. pp. 355–378. ISBN 978-4-431-55641-1.
  5. ^ FRAC (Fungicide Resistance Action Committee) (March 2021). "FRAC Code List ©*2021: Fungal control agents sorted by cross resistance pattern and mode of action (including coding for FRAC Groups on product labels)" (PDF). pp. 1–17. Archived from the original (PDF) on 2021-11-05. Retrieved 2021-07-12.