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Fluopyram

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Fluopyram
Names
Preferred IUPAC name N-{2-ethyl}-2-(trifluoromethyl)benzamide
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.127.749 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C16H11ClF6N2O/c17-12-7-9(15(18,19)20)8-25-13(12)5-6-24-14(26)10-3-1-2-4-11(10)16(21,22)23/h1-4,7-8H,5-6H2,(H,24,26)Key: KVDJTXBXMWJJEF-UHFFFAOYSA-N
SMILES
  • FC(F)(F)c1ccccc1C(=O)NCCc2ncc(cc2Cl)C(F)(F)F
Properties
Chemical formula C16H11ClF6N2O
Molar mass 396.72 g·mol
Melting point 117.5 °C (243.5 °F; 390.6 K)
Boiling point 318–321 °C (604–610 °F; 591–594 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Fluopyram is a fungicide and nematicide used in agriculture. It is used to control fungal diseases such as gray mold (Botrytis cinerea), powdery mildew, apple scab, Alternaria, Sclerotinia, and Monilinia. It is an inhibitor of succinate dehydrogenase (SDHI fungicide).

Developed and produced by Bayer, it was approved in 2012 by the U.S. Environmental Protection Agency and in 2013 it was approved in the EU for use as an active ingredient in pesticides.

References

  1. ^ "Fluopyram" (PDF). Food and Agriculture Organization of the United Nations.
  2. Grabau, Zane J.; Liu, Chang; Schumacher, Lesley A.; Small, Ian M.; Wright, David L. (February 2021). "In-furrow fluopyram nematicide efficacy for Rotylenchulus reniformis management in cotton production". Crop Protection. 140: 105423. doi:10.1016/j.cropro.2020.105423. S2CID 226354918.
  3. Faske, TR; Hurd, K (December 2015). "Sensitivity of Meloidogyne incognita and Rotylenchulus reniformis to Fluopyram". Journal of Nematology. 47 (4): 316–21. PMC 4755706. PMID 26941460.
  4. ^ "Fluopyram". New Active Ingredient Review. Minnesota Department of Agriculture. April 2012. Archived from the original on 2017-04-26. Retrieved 2015-09-16.
  5. "Durchführungsverordnung (EU) Nr. 802/2013 Der Kommission" (in German). August 2013.
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