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AR105900A1 - MOLECULES THAT HAVE PESTICIDE AND INTERMEDIATE UTILITY, COMPOSITIONS AND PROCESSES RELATED TO SUCH MOLECULES - Google Patents

MOLECULES THAT HAVE PESTICIDE AND INTERMEDIATE UTILITY, COMPOSITIONS AND PROCESSES RELATED TO SUCH MOLECULES

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AR105900A1
AR105900A1 ARP160102684A ARP160102684A AR105900A1 AR 105900 A1 AR105900 A1 AR 105900A1 AR P160102684 A ARP160102684 A AR P160102684A AR P160102684 A ARP160102684 A AR P160102684A AR 105900 A1 AR105900 A1 AR 105900A1
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haloalkyl
nrxry
alquilo
het
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A Demeter David
C Sparks Thomas
D Crouse Gary
C Giampietro Natalie
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Dow Agrosciences Llc
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Abstract

La presente descripción se refiere al campo de las moléculas que poseen utilidad plaguicida contra plagas en Phyla Arthropoda, Mollusca, y Nematoda, procesos para producir dichas moléculas, intermediarios utilizados en dichos procesos, composiciones plaguicidas que contienen tales moléculas, y procesos del uso de tales composiciones plaguicidas contra dichas plagas. Estas composiciones plaguicidas se pueden usar, por ejemplo, como acaricidas, insecticidas, miticidas, moluscocidas, y nematicidas. Reivindicación 1: Una molécula que tiene la fórmula (1), donde: (A) Ar¹ se selecciona entre el grupo formado por furanilo, fenilo, piridazinilo, piridilo, pirimidinilo, o tienilo, en donde cada furanilo, fenilo, piridazinilo, piridilo, pirimidinilo, y tienilo pueden ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo, y fenoxi, en donde cada sustituyente de alquilo, haloalquilo, cicloalquilo, alcoxi, haloalcoxi, alquenilo, alquinilo, fenilo y fenoxi puede ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I CN, NO₂, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo, y fenoxi; (B) Het es un anillo heterocíclico saturado o insaturado de 5 ó 6 miembros, que contiene uno o más heteroátomos independientemente seleccionados entre nitrógeno, azufre u oxígeno, y donde Ar¹ y L¹ no son orto entre sí, pero pueden ser meta o para, de modo que, para un anillo de cinco miembros son 1,3 y para un anillo de 6 miembros son 1,3 ó 1,4, en donde cada anillo heterocíclico puede ser opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, oxo, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo, y fenoxi, en donde cada sustituyente de alquilo, haloalquilo, cicloalquilo, alcoxi, haloalcoxi, alquenilo, alquinilo, fenilo y fenoxi puede ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo, y fenoxi; (C) L¹ se selecciona del grupo que consta de O-alquilo C₁₋₄, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-O, O-haloalquilo C₁₋₄, haloalquilo C₁₋₄, haloalquilo C₁₋₄-O, O-cicloalquilo C₃₋₈, cicloalquilo C₃₋₈-O, O-haloalcoxi C₁₋₄, haloalcoxi C₁₋₄-O, O-alquenilo C₂₋₆, alquenilo C₂₋₆-O, O-alquinilo C₂₋₆, y O-alquinilo C₂₋₆, en donde cada alquilo, haloalquilo, cicloalquilo, alquenilo y alquinilo pueden ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, y alquinilo C₂₋₆; (D) Ar² se selecciona entre el grupo formado por furanilo, fenilo, piridazinilo, piridilo, pirimidinilo, o tienilo, en donde cada furanilo, fenilo, piridazinilo, piridilo, pirimidinilo, y tienilo pueden ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I CN, NO₂, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo, y fenoxi, en donde cada sustituyente de alquilo, haloalquilo, cicloalquilo, alcoxi, haloalcoxi, alquenilo, alquinilo, fenilo y fenoxi puede ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(=O)O-alquilo C₁₋₄, fenilo, y fenoxi; (E) R¹⁵ se selecciona entre el grupo formado por H, alquilo C₁₋₄, cicloalquilo C₃₋₈, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, C₍O₎₋NRˣRʸ, C(O)-fenilo, alquilo C₁₋₄-NRˣRʸ, C(O)O-alquilo C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, y alquilo C₁₋₄-OC(=O)O-alquilo C₁₋₄, en donde cada alquilo, cicloalquilo, alquenilo, alquinilo, y fenilo pueden ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, oxo, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄ -O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎ ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo, y fenoxi; (F) Q¹ se selecciona entre el grupo formado por O y S; (G) Q² se selecciona entre el grupo formado por O y S; (H) R¹⁶ se selecciona entre el grupo formado por (K), H, alquilo C₁₋₄, cicloalquilo C₃₋₈, alquenilo C₂₋₆, alquinilo C₂₋₆, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, alquilo C₁₋₄fenilo, alquilo C₁₋₄-O-fenilo, C(O)-(Het-1), Het-1, alquilo C₁₋₄-(Het-1), alquilo C₁₋₄-OC(O)-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)O-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-NRˣRʸ, alquilo C₁₋₄-C(O)-N(Rˣ)-alquilo C₁₋₄-(Het-1), alquilo C₁₋₄-C(O)-(Het-1), alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄(NRˣRʸ)-C(O)OH, alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄-NRˣRʸ, alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄-N(Rˣ)-C(O)O-alquilo C₁₋₄, alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄, (N(Rˣ)-C(O)O-alquilo C₁₋₄)-C(O)OH, alquilo C₁₋₄-C(O)-(Het-1)-C(O)O-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)O-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-cicloalquilo C₃₋₈, alquilo C₁₋₄-OC(O)-(Het-1), alquilo C₁₋₄-OC(O)alquilo C₁₋₄-N(Rˣ)-C(O)O-alquilo C₁₋₄, alquilo C₁₋₄-NRˣRʸ, alquilo C₁₋₄-S(O)ₙ-(Het-1), y alquilo C₁₋₄-O-(Het-1), en donde cada alquilo, cicloalquilo, alquenilo, alquinilo, fenilo, y (Het-1) pueden ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, NRˣRʸ, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎H, C₍O₎OH, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo, fenoxi, Si(alquilo C₁₋₄)₃, S(O)ₙ-NRˣRʸ, y (Het-1); (I) R¹⁷ se selecciona entre el grupo formado por (K), H, alquilo C₁₋₄, cicloalquilo C₃₋₈, alquenilo C₂₋₆, alquinilo C₂₋₆, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, alquilo C₁₋₄fenilo, alquilo C₁₋₄-O-fenilo, C(O)-(Het-1), (Het-1), alquilo C₁₋₄-(Het-1), alquilo C₁₋₄-OC(O)-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)O-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-NRˣRʸ, alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄-(Het-1), alquilo C₁₋₄-C(O)-(Het-1), alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄(NRˣRʸ)-C(O)OH, alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄-NRˣRʸ, alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄-N(Rˣ)-C(O)O-alquilo C₁₋₄, alquilo C₁₋₄-C(O)-N(Rˣ)alquilo C₁₋₄(N(Rˣ)-C(O)O-alquilo C₁₋₄)-C(O)OH, alquilo C₁₋₄-C(O)-(Het-1)-C(O)O-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)O-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-alquilo C₁₋₄, alquilo C₁₋₄-OC(O)-cicloalquilo C₃₋₈, alquilo C₁₋₄-OC(O)-(Het-1), alquilo C₁₋₄-OC(O)-alquilo C₁₋₄-N(Rˣ)-C(O)O-alquilo C₁₋₄, alquilo C₁₋₄-NRˣRʸ, alquilo C₁₋₄S(O)ₙ-(Het-1), y alquilo C₁₋₄-O-(Het-1), en donde cada alquilo, cicloalquilo, alquenilo, alquinilo, fenilo, y (Het-1) pueden ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, NRˣRʸ, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎H, C₍O₎OH, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, alquilo C₁₋₄-O-alquilo C₁₋₄, alquilo C₁₋₄-S(O)ₙ-alquilo C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C(O)O-alquilo C₁₋₄, fenilo fenoxi, Si(alquilo C₁₋₄)₃, S(O)ₙ-NRˣRʸ, y (Het-1); (J) L² se selecciona entre el grupo formado por cicloalquilo C₃₋₈, fenilo, alquilo C₁₋₄fenilo, alquilo C₁₋₄-O-fenilo, alquenil C₂₋₆-O-fenilo, (Het-1), alquilo C₁₋₄-(Het-1), y alquilo C₁₋₄-O-(Het-1), en donde cada alquilo, cicloalquilo, alquenilo, fenilo, y (Het-1) pueden ser opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados entre el grupo formado por H, F, Cl, Br, I, CN, NO₂, NRˣRʸ, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₈, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, S(O)ₙ-alquilo C₁₋₄, S(O)ₙ-haloalquilo C₁₋₄, OSO₂-alquilo C₁₋₄, OSO₂-haloalquilo C₁₋₄, C₍O₎H, C₍O₎₋NRˣRʸ, alquilo C₁₋₄-NRˣRʸ, C(O)-alquilo C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, O-alquilo C₁₋₄, S-alquilo C₁₋₄, alquilo C₁₋₄-O-alquilo C₁₋₄,The present description refers to the field of molecules that have pesticide utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes for producing said molecules, intermediates used in said processes, pesticidal compositions containing such molecules, and processes for the use of such pesticidal compositions against said pests. These pesticidal compositions can be used, for example, as acaricides, insecticides, miticides, molluscides, and nematicides. Claim 1: A molecule having the formula (1), wherein: (A) Ar¹ is selected from the group consisting of furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, or thienyl, wherein each furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, and thienyl can be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO₂, C alquilo alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, alkoxy C₁₋₄, C₁₋₄ haloalkoxy, C₂₋₆ alkenyl, C₂₋₆ alkynyl, S (O) ₙ -C₁₋₄ alkyl, S (O) ₙ -C₁₋₄ haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂- haloalkyl C₁₋₄, C₍O₎₋NRˣRʸ, alkyl C₁₋₄-NRˣRʸ, C (O) -alkyl C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜ ₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄-O-C alquilo alkyl, C₁₋₄-S (O) ₙ-alkyl C₁₋₄, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl, and phenoxy, wherein each substituent of alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, phenyl and phenoxy may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I CN, NO₂, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy , C₁₋₄ haloalkoxy, C₂₋₆ alkenyl, C₂₋₆ alkynyl, S (O) ₙ -C₁₋₄ alkyl, S (O) ₙ -C halo haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋ haloalkyl ₄, C₍O₎₋NRˣRʸ, C₁₋₄-NRˣRʸ alkyl, C (O) -C₁₋₄ alkyl, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒ ₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O ₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄-O-alkyl C alquilo, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl, and phenoxy; (B) Het is a saturated or unsaturated 5 or 6 membered heterocyclic ring, which contains one or more heteroatoms independently selected from nitrogen, sulfur or oxygen, and where Ar¹ and L¹ are not orthopedic, but may be meta or para, so that, for a five-member ring they are 1.3 and for a 6-member ring they are 1.3 or 1.4, where each heterocyclic ring can be optionally substituted with one or more substituents independently selected from the group formed by H, F, Cl, Br, I, CN, NO₂, oxo, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₂₋₆ alkenyl, C₂₋ alkynyl ₆, S (O) ₙ-C₁₋₄ alkyl, S (O) ₙ-C halo haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍O₎₋NRˣRʸ, C₁₋₄- alkyl NRˣRʸ, C (O) -alkyl C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍ O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆ , C₁₋₄-O-C₁₋₄ alkyl, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl, and phenoxy, wherein each substituent of alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, phenyl and phenoxy may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br , I, CN, NO₂, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₂₋₆ haloalkoxy, C₂₋₆ alkynyl, C₂₋₆ alkynyl, S (O) ₙ-C alquilo alkyl ₋₄, S (O) ₙ-C₁₋₄ haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍O₎ ₋NRˣRʸ, C₁₋₄-NRˣRʸ alkyl, C (O) -C₁₋₄ alkyl, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋ ₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄-O alkyl -C₁₋₄ alkyl, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl, and phenoxy; (C) L¹ is selected from the group consisting of O-C₁₋₄ alkyl, C₁₋₄-O-C₁₋₄ alkyl, C₁₋₄-O alkyl, O-haloalkyl C₁₋₄, haloalkyl C₁₋₄, haloalkyl C₁₋₄-O, C₃₋₈-O-cycloalkyl, C₃₋₈-O cycloalkyl, C O-O-haloalkoxy, C₁₋₄-O haloalkoxy, C₂₋₆-O-alkenyl, C₂₋₆-O-alkenyl, O- C₂₋₆ alkynyl, and C₂₋₆ O-alkynyl, wherein each alkyl, haloalkyl, cycloalkyl, alkenyl and alkynyl can be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I , CN, NO₂, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₂₋₆ alkenyl, and C₂₋₆ alkynyl; (D) Ar² is selected from the group consisting of furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, or thienyl, wherein each furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, and thienyl can be optionally substituted with one or more independently selected substituents between the group consisting of H, F, Cl, Br, I CN, NO₂, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₂₋₆ alkenyl, C₂ alkynyl ₋₆, S (O) ₙ-C₁₋₄ alkyl, S (O) ₙ-C halo haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍O₎₋NRˣRʸ, C₁₋₄ alkyl -NRˣRʸ, C (O) -alkyl C₁₋₄, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱ ₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄-O-alkyl C₁₋₄, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl, and phenoxy, wherein each substituent of alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, phenyl and phenoxy may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO₂, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₂₋ alkenyl ₆, C₂₋₆ alkynyl, S (O) ₙ-C₁₋₄ alkyl, S (O) ₙ -C₁₋₄ haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍O₎₋NRˣRʸ, C₁₋₄-NRˣRʸ, C (O) -C₁₋₄ alkyl, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱ ₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋ alkyl ₄-O-C₁₋₄ alkyl, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (= O) O-C₁₋₄ alkyl, phenyl, and phenoxy; (E) R¹⁵ is selected from the group consisting of H, C₁₋₄ alkyl, C₃₋₈ cycloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, S (O) ₙ-C₁₋₄ alkyl, C₍O₎₋NRˣRʸ , C (O) -phenyl, C₁₋₄-NRˣRʸ alkyl, C (O) O-C₁₋₄ alkyl, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O ₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄-O-alkyl-C₁₋₄ alkyl, C₁₋₄-OC (O) alkyl-C₁₋₄ alkyl, C₁₋₄- alkyl S (O) ₙ-C₁₋₄ alkyl, and C₁₋₄-OC (= O) O-C₁₋₄ alkyl, wherein each alkyl, cycloalkyl, alkenyl, alkynyl, and phenyl may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO₂, oxo, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, al C₂₋₆ nyl, C₂₋₆ alkynyl, S (O) ₙ-C₁₋₄ alkyl, S (O) ₙ -C halo haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍O₎ ₋NRˣRʸ, C₁₋₄-NRˣRʸ alkyl, C (O) -C₁₋₄ alkyl, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋ ₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄ -O alkyl -C₁₋₄ alkyl, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎ ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl, and phenoxy; (F) Q¹ is selected from the group consisting of O and S; (G) Q² is selected from the group consisting of O and S; (H) R¹⁶ is selected from the group consisting of (K), H, C₁₋₄ alkyl, C₃₋₈ cycloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄, C₁₋ alkyl ₄-O-C₁₋₄ alkyl, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₁₋₄phenyl alkyl, C₁₋₄-O-phenyl alkyl, C (O) - (Het-1), Het-1, C₁₋₄- (Het-1) alkyl, C₁₋₄-OC (O) alkyl-C₁₋₄ alkyl, C₁₋₄-OC (O) alkyl-C₁₋₄ alkyl, C₁₋₄- alkyl OC (O) O-C₁₋₄ alkyl, C₁₋₄-OC (O) -NRˣRʸ alkyl, C₁₋₄-C (O) -N (Rˣ) -C₁₋₄- (Het-1) alkyl, alkyl C₁₋₄-C (O) - (Het-1), C₁₋₄-C (O) -N (Rˣ) alkyl C₁₋₄ (NRˣRʸ) -C (O) OH, C₁₋₄-C alkyl ( O) -N (Rˣ) C₁₋₄-NRˣRʸ alkyl, C₁₋₄-C (O) -N (Rˣ) alkyl C₁₋₄-N (Rˣ) -C (O) O-C₁₋₄ alkyl, alkyl C₁₋₄-C (O) -N (Rˣ) C₁₋₄ alkyl, (N (Rˣ) -C (O) O-C₁₋₄ alkyl) -C (O) OH, C₁₋₄-C alkyl (O ) - (Het-1) -C (O) O-C₁₋₄ alkyl , C₁₋₄-OC (O) O-C₁₋₄ alkyl, C₁₋₄-OC (O) alkyl-C₁₋₄ alkyl, C₁₋₄-OC (O) alkyl-C alquilo cycloalkyl, C₁₋ alkyl ₄-OC (O) - (Het-1), C₁₋₄-OC (O) alkyl C₁₋₄-N (Rˣ) -C (O) O-C₁₋₄ alkyl, C₁₋₄-NRˣRʸ alkyl, C₁₋₄-S (O) ₙ- (Het-1) alkyl, and C₁₋₄-O- (Het-1) alkyl, wherein each alkyl, cycloalkyl, alkenyl, alkynyl, phenyl, and (Het-1) they may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO₂, NRˣRʸ, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋ alkoxy ₄, C₂₋₆ alkenyl, C₂₋₆ alkynyl, S (O) ₙ-C₁₋₄ alkyl, S (O) ₙ -C halo haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍ O₎H, C₍O₎OH, C₍O₎₋NRˣRʸ, C₁₋₄-NRˣRʸ alkyl, C (O) -C₁₋₄ alkyl, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ ₕₐₗ ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O ₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄-O-alkyl C alquilo, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl, phenoxy, Si (C₁₋₄ alkyl) ₃, S (O) ₙ-NRˣRʸ, and (Het-1); (I) R¹⁷ is selected from the group consisting of (K), H, C₁₋₄ alkyl, C₃₋₈ cycloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄, C₁₋ alkyl ₄-O-C₁₋₄ alkyl, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₁₋₄phenyl alkyl, C₁₋₄-O-phenyl alkyl, C (O) - (Het-1), (Het-1), C₁₋₄- (Het-1) alkyl, C₁₋₄-OC (O) alkyl-C₁₋₄ alkyl, C₁₋₄-OC (O) alkyl-C₁₋₄ alkyl, C₁₋ alkyl ₄-OC (O) O-C₁₋₄ alkyl, C₁₋₄-OC (O) -NRˣRʸ alkyl, C₁₋₄-C (O) -N (Rˣ) C₁₋₄- (Het-1) alkyl, C₁₋₄-C (O) - (Het-1) alkyl, C₁₋₄-C (O) -N (Rˣ) C₁₋₄ (NRˣRʸ) -C (O) OH alkyl, C₁₋₄-C alkyl (O) -N (Rˣ) C₁₋₄-NRˣRʸ alkyl, C₁₋₄-C (O) -N (Rˣ) alkyl C₁₋₄-N (Rˣ) -C (O) O-C₁₋₄ alkyl, C₁₋₄-C (O) -N (Rˣ) alkyl C₁₋₄ (N (Rˣ) -C (O) O-C₁₋₄ alkyl) -C (O) OH, C₁₋₄-C (O) alkyl ) - (Het-1) -C (O) O-C₁₋₄ alkyl, C₁₋₄-OC (O) O-C₁₋₄-alkyl, C₁₋₄-OC (O) -C₁₋₄-alkyl, C₁₋₄-OC (O) -C₃₋₈ -alkyl alkyl, C alquilo-alkyl -OC (O) - (Het-1), C₁₋₄-OC (O) alkyl-C₁₋₄-N (Rˣ) -C (O) O-C₁₋₄ alkyl, C₁₋₄-NRˣRʸ alkyl, C₁₋₄S (O) ₙ- (Het-1) alkyl, and C₁₋₄-O- (Het-1) alkyl, wherein each alkyl, cycloalkyl, alkenyl, alkynyl, phenyl, and (Het-1) may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO₂, NRˣRʸ, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₂₋₆ alkenyl, C₂₋₆ alkynyl, S (O) ₙ-C₁₋₄ alkyl, S (O) ₙ -Chaloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍O₎ H, C₍O₎OH, C₍O₎₋NRˣRʸ, C₁₋₄-NRˣRʸ alkyl, C (O) -C₁₋₄ alkyl, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗ ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O ₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₁₋₄-O-alkyl C alquilo, C₁₋₄-S (O) alkyl ₙ-C₁₋₄ alkyl, C₍O₎₋ₐₗqᵘⁱₗₒ C₁₋₄-C (O) O-C₁₋₄ alkyl, phenyl phenoxy, Si (C₁₋₄ alkyl) ₃, S (O) ˣ-NRˣRʸ, and (Het-1); (J) L² is selected from the group consisting of C₃₋₈ cycloalkyl, phenyl, C₁₋₄phenyl alkyl, C₁₋₄-O-phenyl alkyl, C₂₋₆-O-phenyl alkenyl, (Het-1), C₁₋ alkyl ₄- (Het-1), and C₁₋₄-O- (Het-1) alkyl, wherein each alkyl, cycloalkyl, alkenyl, phenyl, and (Het-1) may be optionally substituted with one or more independently selected substituents between the group consisting of H, F, Cl, Br, I, CN, NO₂, NRˣRʸ, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₂₋₆ alkenyl , C₂₋₆ alkynyl, S (O) ₙ-C₁₋₄ alkyl, S (O) ₙ -C₁₋₄ haloalkyl, OSO₂-C₁₋₄ alkyl, OSO₂-C₁₋₄ haloalkyl, C₍O₎H, C₍ O₎₋NRˣRʸ, C₁₋₄-NRˣRʸ alkyl, C (O) -C₁₋₄ alkyl, C₍O₎O₋ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎O₋ₕₐₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ᶜⁱᶜₗ ₒₐₗqᵘⁱₗₒ C₃₋₈, C₍O₎O₋ᶜⁱᶜₗₒₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, C₍O₎O₋ₐₗqᵘₑₙⁱₗₒ C₂₋₆, O-C₁₋₄ alkyl, S-C₁₋₄ alkyl , C₁₋₄-O-C₁₋₄ alkyl,

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CN112029681A (en) * 2020-08-26 2020-12-04 四川师范大学 Preparation of special liquid composite microbial inoculum for decomposing vinasse
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