Cyantraniliprole

Source: Wikipedia, the free encyclopedia.
Cyantraniliprole
Names
Preferred IUPAC name
4-Bromo-1-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(N-methylcarbamoyl)phenyl]-1H-pyrazole-5-carboxamide
Other names
Cyazypyr; Exirel
Identifiers
3D model (
JSmol
)
ChEBI
ChemSpider
ECHA InfoCard
 100.205.162 Edit this at Wikidata
UNII
  • InChI=1S/C19H14BrClN6O2/c1-10-6-11(9-22)7-12(18(28)23-2)16(10)25-19(29)14-8-15(20)26-27(14)17-13(21)4-3-5-24-17/h3-8H,1-2H3,(H,23,28)(H,25,29)
    Key: DVBUIBGJRQBEDP-UHFFFAOYSA-N
  • InChI=1/C19H14BrClN6O2/c1-10-6-11(9-22)7-12(18(28)23-2)16(10)25-19(29)14-8-15(20)26-27(14)17-13(21)4-3-5-24-17/h3-8H,1-2H3,(H,23,28)(H,25,29)
    Key: DVBUIBGJRQBEDP-UHFFFAOYAE
  • CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)C#N
Properties
C19H14BrClN6O2
Molar mass 473.72 g·mol−1
Melting point 217-219 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Cyantraniliprole is an insecticide of the ryanoid class, specifically a diamide insecticide (IRAC MoA group 28).[1] It is approved for use in the United States, Canada, China, and India.[2] Because of its uncommon mechanism of action as a ryanoid, it has activity against pests such as Diaphorina citri that have developed resistance to other classes of insecticides.[3]

As part of an ongoing court dispute by the

Endangered Species Act, and put in place appropriate protections.[4]

References

  1. ^ IRAC International MoA Working Group (March 2020). "IRAC Mode of Action Classification Scheme Version 9.4". Insecticide Resistance Action Committee.
  2. ^ "Australia to approve DuPont's Exirel insecticide cyantraniliprole". AgroNews. Oct 10, 2013.
  3. PMID 23371893
    .
  4. ^ Legal Victory: Court Orders EPA to Protect Endangered Wildlife From Toxic Pesticide
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