1355342-91-4

Upstream product

• 1355345-65-1 1,1-dimethylethyl 3-[[5,6-dichloro-3-[[(2-chloro-4-pyridinyl)carbonyl]amino]-2-pyridinyl]oxy]-1-azetidinecarboxylate 
• 1355345-64-0 1,1-dimethylethyl 3-[(3-amino-5,6-dichloro-2-pyridinyl)oxy]-1-azetidinecarboxylate 
• 1355345-61-7 1,1-dimethylethyl 3-[(3-amino-5-chloro-2-pyridinyl)oxy]-1-azetidinecarboxylate 
• 1355345-60-6 1,1-dimethylethyl 3-[(5-chloro-3-nitro-2-pyridinyl)oxy]-1-azetidinecarboxylate 
• 21427-61-2 5-chloro-3-nitropyridin-2(1H)-one 

Relevant academic research and scientific papers

PESTICIDAL 3-(ARYLOXY)AZACYCLOALKANES

Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, wherein A1 is N or CR7; A2 is N or CR8;A3 is N or CR9; A4 is N or CR10; provided that not more than two of A1, A2, A3 and A4 are N; T is O, S(O)k or NR36; L is -C(R11)=C(R12)-, wherein the carbon atom bonded to R11 is also bonded to CR4R5 and the carbon atom bonded to R12 is also bonded to R6; or 1,4-diphenylene optionally substituted with up to 4 substituents independently selected from R13; or C(R34)(R35)-Z-, wherein the carbon atom bonded to R34 and R35 is also bonded to CR4R5 and Z is bonded to R6; Z is O, S(O)m, NR37 or CR38R39; R1 is a phenyl or 5- or 6-membered heteroaromatic ring optionally substituted with up to 5 substituents independently selected from R14; R6 is a phenyl or 5- or 6-membered heteroaromatic ring optionally substituted with up to 5 substituents independently selected from R22; s is 1, 2 or 3; t is 1 or 2; provided that the sum of s and t is 2, 3 or 4; and R2, R3, R4, R5, R7, R8, R9, R10, R11, R12, R13, R14, R22, R34, R35, R36, R37, R38, R39, W, k, m and n are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.