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Cyantraniliprole

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Cyantraniliprole
Names
IUPAC name
3-Bromo-1-(3-chloro-2-pyridinyl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-1H-pyrazole-5-carboxamide
Other names
Cyazpyr; Exirel
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.205.162 Edit this at Wikidata
  • 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
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. It is approved for use in the United States, Canada, China, and India.[1] 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 insecticides.[2] Cyantraniliprole is highly toxic to bees, which resulted in registration of its use as a pesticide being delayed in the USA.[3]

References

  1. ^ "Australia to approve DuPont's Exirel insecticide cyantraniliprole". AgroNews. Oct 10, 2013.
  2. ^ Tiwari S, Stelinski LL (Sep 2013). "Effects of cyantraniliprole, a novel anthranilic diamide insecticide, against Asian citrus psyllid under laboratory and field conditions". Pest Manag Sci. 69 (9): 1066–1072. doi:10.1002/ps.3468.
  3. ^ http://chemlinked.com/news/agrochemical-news/statistics-expert-review-icama-registration-h2-2012
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