Cyantraniliprole

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
CAS Number	736994-63-1 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:132300
ChemSpider	9753377
ECHA InfoCard	100.205.162
PubChem CID	11578610
UNII	LO6K6H48FD Y
CompTox Dashboard (EPA)	DTXSID2058174
InChI 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
SMILES CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)C#N
Properties
Chemical formula	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). Infobox references

Cyantraniliprole is an insecticide of the ryanoid class, specifically a diamide insecticide (IRAC MoA group 28). It is approved for use in the United States, Canada, China, and India. 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.

As part of an ongoing court dispute by the Center for Biological Diversity, in November 2022, the U.S. Court of Appeals for the D.C. Circuit ordered the United States Environmental Protection Agency to consider harms to plants and animals under the Endangered Species Act, and put in place appropriate protections.