Chlorantraniliprole

Chlorantraniliprole is an insecticide of the diamide class used for insects found on fruit and vegetable crops as well as ornamental plants.^[1]

Chlorantraniliprole

Chlorantraniliprole 3D molecular model generated using Avogadro software
Names
Preferred IUPAC name 3-Bromo-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide
Other names Rynaxypyr, Coragen, Altacor
Identifiers
CAS Number	500008-45-7
3D model (JSmol)	Interactive image
Beilstein Reference	11247880
ChEBI	CHEBI:67113
ChEMBL	ChEMBL399318
ChemSpider	9446648
ECHA InfoCard	100.112.607
EC Number	610-489-8
KEGG	C18454
PubChem CID	11271640
UNII	622AK9DH9G
CompTox Dashboard (EPA)	DTXSID2044345
InChI InChI=1S/C18H14BrCl2N5O2/c1-9-6-10(20)7-11(17(27)22-2)15(9)24-18(28)13-8-14(19)25-26(13)16-12(21)4-3-5-23-16/h3-8H,1-2H3,(H,22,27)(H,24,28) Key: PSOVNZZNOMJUBI-UHFFFAOYSA-N
SMILES CC1=C(C(=CC(=C1)Cl)C(=O)NC)NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br
Properties
Chemical formula	C18H14BrCl2N5O2
Molar mass	483.15 g·mol−1
Melting point	209 °C (408 °F; 482 K)
Hazards
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H319, H335, H410
Precautionary statements	P261, P264, P271, P273, P280, P304+P340, P305+P351+P338, P312, P337+P313, P391, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Chlorantraniliprole opens muscular calcium channels, in particular the ryanodine receptor, rapidly causing paralysis and ultimately death of sensitive species (IRAC class 28). The differential selectivity chlorantraniliprole has towards insect ryanodine receptors explains its low mammalian toxicity receptor.^[2] Chlorantraniliprole is active on chewing pest insects primarily by ingestion and secondarily by contact.