The same is true of the use of anthrax compounds or compounds containing anthrax compounds to control invertebrate pests. In addition, methods of using these compounds. Requirement 1: one part of the compound of general formula (1), wherein A1,...A3 and a830808 are n or CH, but up to January 2, A1,...A3 and a8308sean n； B1 is n or CH； G is a formula group (2), where q is O, n (r8313)； 74919, or chemical link； r7501 is selected from hydrogen, halogen, cyanogen, nitrogen SNA, sf832525；1. Lease land No. c833218331 and 832626；C₁₋₆ haloalkyl,C₁₋₆ alkoxy-C₁₋₆ alkyl,C₂₋₆ alkenyl,C₂₋₆ haloalkenyl,1. C 83228331 asphalt；C₂₋₆ haloalkynyl,C₃₋₈ cycloalkyl,Halogenated ring 12-Yes (r830808) 8322； R3,-Or831222,-OSO₂R⁸,-831222,-S (O) R-S (O) N (R) R-N (R) R-C (3DO) N (R) R-C (3DS) N (R) R-C (3DO) OR-C (O) R1. Phenyl which can be replaced by 1,2,3,4 or 5 R1 83044；1. 2, 3, 4 or 5 R1 830404 replaceable reference；And a saturated, partially or completely unsaturated acyclic ring composed of 3, 4, 5, 6 or 7 members, including 1, 2 or 3 heteroatoms or groups selected from n, O, s, no, so and so；a. As a member of the ring, the heterocycle of the ring can be replaced by one or more r183044 type radicals；Rʰ is selected from the group consisting of hydrogen, cyano, C₁₋₆ alkyl,C₁₋₆ haloalkyl,C₁₋₆ alkoxy,C₁₋₆ haloalkoxy,1. C8332121 asphalt；Halogenated tar c83217c831832626；C₁₋₆ alkylsulfinyl,C₁₋₆ haloalkylsulfinyl,C₁₋₆ alkylsulfonyl,1. Halogen glycol c83216c83183226；C₃₋₈ cycloalkyl,C83238c83287287c83218c833183248aje - lessor c83321218c8331248c83324；Halogenated ring 12C₂₋₆ alkenyl,C₂₋₆ haloalkenyl,1. C 83228331 asphalt；C₂₋₆ haloalkynyl,-Yes (r830808) 8322； R3,-831222,-S (O) R-S (O) N (R) R-N (R) R-N = CR¹⁵R¹⁶,-C (3DO) R-C (3DO) N (R) R-C (3DS) N (R) R-C (3DO) OR1. Phenyl which can be replaced by 1,2,3,4 or 5 R1 83044；And a saturated, partially or completely unsaturated acyclic ring composed of 3, 4, 5, 6 or 7 members, including 1, 2 or 3 heteroatoms or groups selected from n, O, s, no, so and so；a
