AR114040A1 - BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES - Google Patents

BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES

Info

Publication number
AR114040A1
AR114040A1 ARP180103823A ARP180103823A AR114040A1 AR 114040 A1 AR114040 A1 AR 114040A1 AR P180103823 A ARP180103823 A AR P180103823A AR P180103823 A ARP180103823 A AR P180103823A AR 114040 A1 AR114040 A1 AR 114040A1
Authority
AR
Argentina
Prior art keywords
alkyl
group
alkoxy
cycloalkyl
phenyl
Prior art date
Application number
ARP180103823A
Other languages
Spanish (es)
Original Assignee
Basf Se
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Basf Se filed Critical Basf Se
Publication of AR114040A1 publication Critical patent/AR114040A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/081,2,5-Oxadiazoles; Hydrogenated 1,2,5-oxadiazoles
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647Triazoles; Hydrogenated triazoles
    • A01N43/6531,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/713Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/82Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D249/14Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D257/00Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04Five-membered rings
    • C07D257/06Five-membered rings with nitrogen atoms directly attached to the ring carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/101,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
    • C07D271/1131,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

Compuestos de benzamida de la fórmula (1), en donde las variables se definen en las reivindicaciones y la descripción, los N-óxidos y sus sales, y composiciones que las comprenden. También el uso de los compuestos de benzamida, o de las composiciones que comprenden tales compuestos para controlar la vegetación no deseada, y un método para controlar la vegetación no deseada mediante la aplicación de dichos compuestos o composiciones. Reivindicación 1: Un compuesto caracterizado por la fórmula (1), en donde Q es un compuesto de fórmula Q¹ o Q² o Q³ o Q⁴, del grupo de fórmulas (2), en donde # representa el punto de unión con el resto de la molécula; R¹ se selecciona del grupo que consiste en ciano, halógeno, nitro, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₂₋₈-alquenilo, C₂₋₈-alquinilo, C₁₋₄-alcoxi-C₁₋₄-alquilo, C₁₋₄-haloalcoxi-C₁₋₄-alquilo, C₁₋₈-alcoxi, C₁₋₆-haloalcoxi, C₁₋₄-alcoxi-C₁₋₄-alcoxi-Z¹ y R¹ᵇ-S(O)ₖ-Z¹; R² se selecciona del grupo que consiste en fenil-Z⁴-S(O)ₙ-Z², heterociclil-Z⁴-S(O)ₙ-Z², Cyc-Z⁴-S(O)ₙ-Z² y Het-Z²ᵃ, en donde los grupos cíclicos de los cuatro radicales antes mencionados son no sustituidos o sustituidos con 1, 2, 3 ó 4 sustituyentes seleccionados, independientemente entre sí, del grupo que consiste en halógeno, nitro, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi, C₁₋₄-haloalcoxi, C₁₋₄-alquilsulfonilo, C₁₋₄-haloalquilsulfonilo, fenilo y oxo; en donde Cyc es C₃₋₆-cicloalquilo o C₃₋₆-cicloalquilo fusionado a un anillo de benceno; en donde el heterociclilo es un heterociclo monocíclico de 3, 4, 5 ó 6 miembros o bicíclico de 7, 8, 9 ó 10 miembros saturado, parcialmente insaturado o totalmente insaturado que contiene 1, 2, 3 ó 4 heteroátomos seleccionados del grupo que consiste en O, N y S(O)ₙ como miembros del anillo; y en donde Het es un heterociclo de 5 ó 6 miembros saturado que contiene 1 ó 2 grupos S(O)ₙ como miembros del anillo; R³ se selecciona del grupo que consiste en hidrógeno, ciano, tiocianato, halógeno, nitro, hidroxi-Z³, C₁₋₈-alquilo, C₁₋₄-cianoalquilo, C₁₋₈-haloalquilo, C₂₋₈-alquenilo, C₂₋₈-haloalquenilo, C₂₋₈-alquinilo, C₃₋₈-haloalquinilo, C₃₋₁₀-cicloalquil-Z³, C₃₋₆-cicloalquenil-Z³, C₃₋₁₀-cicloalcoxi-Z³, C₃₋₁₀-cicloalquil-C₁₋₂-alcoxi, en donde los grupos cíclicos de los cuatro radicales antes mencionados son no sustituidos o parcial o totalmente halogenados; C₁₋₈-alcoxi-Z³, C₁₋₈-haloalcoxi-Z³, C₁₋₄-alcoxi-C₁₋₄-alcoxi-Z³, C₁₋₄-haloalcoxi-C₁₋₄-alcoxi-Z³, C₂₋₈-alqueniloxi-Z³, C₂₋₈-haloalqueniloxi-Z³, C₂₋₈-alquiniloxi-Z³, C₃₋₈-haloalquiniloxi-Z³, R³ᵇ-S(O)ₖ-Z³, R³ᶜ-C(O)-Z³, R³ᵈO-C(O)-Z³, R³ᵈO-N=CH-Z³, R³ᵉR³ᶠN-C(O)-Z³, R³ᵍR³ʰN-Z³, R²²C(O)O-Z³, R²⁵OC(O)O-Z³, (R²²)₂NC(O)O-Z³, R²⁵S(O)₂O-Z³, R²²OS(O)₂-Z³, (R²²)₂NS(O)₂-Z³, R²⁵OC(O)N(R²²)-Z³, (R²²)₂NC(O)N(R²²)-Z³, (R²²)₂NS(O)₂N(R²²)-Z³, (OH)₂P(O)-Z³, (C₁₋₄-alcoxi)₂P(O)-Z³, fenil-Z³ᵃ y heterociclil-Z³ᵃ, en donde el heterociclilo es un heterociclo monocíclico de 3, 4, 5 ó 6 miembros o bicíclico de 8, 9 ó 10 miembros saturado, parcialmente insaturado o aromático que contiene 1, 2, 3 ó 4 heteroátomos seleccionados del grupo que consiste en O, N y S como miembros del anillo; en donde los grupos cíclicos en fenil-Z³ᵃ y heterociclil-Z³ᵃ son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos R²¹ que son idénticos o diferentes; en donde R³ no es nitro si R² es fenil-S(O)ₙ-Z² o C₃₋₆-cicloalquil-S(O)ₙ-Z²; R⁴ se selecciona del grupo que consiste en hidrógeno, halógeno, nitro, ciano-Z¹, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₃₋₇-cicloalquil-C₁₋₄-alquilo, en donde los grupos C₃₋₇-cicloalquilo en los dos radicales antes mencionados son no sustituidos o parcial o totalmente halogenados; C₂₋₈-alquenilo, C₂₋₈-alquinilo, C₁₋₃-alquilamino, di-(C₁₋₃-alquil)-amino, C₁₋₃-alquilamino-S(O)ₖ, C₁₋₃-alquilcarbonilo, C₁₋₈-alcoxi, C₁₋₆-haloalcoxi, C₁₋₄-alcoxi-C₁₋₄-alquilo, C₁₋₄-haloalcoxi-C₁₋₄-alquilo, C₁₋₄-alcoxi-C₁₋₄-alcoxi-Z¹, C₁₋₄-haloalcoxi-C₁₋₄-alcoxi-Z¹, C₁₋₄-alquitio-C₁₋₄-alquiltio-Z¹, C₂₋₆-alqueniloxi, C₂₋₆-alquiniloxi, R¹ᵇ-S(O)ₖ-Z¹, fenoxi-Z¹ y heterocicliloxi-Z¹, en donde heterocicliloxi es un heterociclo monocíclico de 5 ó 6 miembros o bicíclico de 8, 9 ó 10 miembros saturado unido a oxígeno que contiene 1, 2, 3 ó 4 heteroátomos seleccionados del grupo que consiste en O, N y S como miembros del anillo; en donde los grupos cíclicos en fenoxi y heterocicliloxi son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos R¹¹ que son idénticos o diferentes; cada R⁵ se selecciona independientemente del grupo que consiste en C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₃₋₇-cicloalquil-C₁₋₄-alquilo, en donde los grupos C₃₋₇-cicloalquilo de los dos radicales antes mencionados son no sustituidos o parcial o totalmente halogenados; C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₄-alcoxi-C₁₋₄-alquilo, C₁₋₄-haloalcoxi-C₁₋₄-alquilo, Rᵇ-S(O)ₙ-C₁₋₃-alquilo, fenilo y bencilo, en donde fenilo y bencilo son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; en donde R⁵ no es C₁₋₄-alcoxi-C₁₋₄-alquilo si R² es C₃₋₆-cicloalquil-S(O)ₙ-Z²; R¹¹ y R²¹ se seleccionan, independientemente, entre sí, del grupo que consiste en ciano, halógeno, nitro, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₃₋₇-halocicloalquilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₁₋₆-alcoxi-C₁₋₄-alquilo, C₁₋₄-haloalcoxi-C₁₋₄-alquilo, C₁₋₄-alquiltio-C₁₋₄-alquilo, C₁₋₄-alcoxi-C₁₋₄-alcoxi y C₃₋₇-cicloalcoxi, o dos radicales R²¹ unidos al mismo átomo de carbono de heterociclilo juntos pueden formar un grupo =O; Z¹ y Z³ se seleccionan, independientemente entre sí, del grupo que consiste en un enlace covalente y C₁₋₄-alcandiilo; Z² es C₁₋₃-alcandiilo que es no sustituido o sustituido con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en C₁₋₄-alquilo y C₁₋₄-haloalquilo; Z²ᵃ es un enlace covalente o C₁₋₃-alcandiilo que es no sustituido o sustituido con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en C₁₋₄-alquilo y C₁₋₄-haloalquilo; Z³ᵃ se selecciona del grupo que consiste en un enlace covalente, C₁₋₄-alcandiilo, O-C₁₋₄-alcandiilo, C₁₋₄-alcandiil-O y C₁₋₄-alcandiil-O-C₁₋₄-alcandiilo; Z⁴ es un enlace covalente o C₁₋₃-alcandiilo; Rᵇ, R¹ᵇ y R³ᵇ se seleccionan, independientemente entre sí, del grupo que consiste en C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, fenilo y heterociclilo, en donde heterociclilo es un heterociclo monocíclico de 5 ó 6 miembros saturado, parcialmente insaturado o aromático que contiene 1, 2, 3 ó 4 heteroátomos seleccionados del grupo que consiste en O, N y S como miembros del anillo, en donde fenilo y heterociclilo son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; R³ᶜ se selecciona del grupo que consiste en hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₃₋₇-cicloalquil-C₁₋₄-alquilo, en donde los grupos C₃₋₇-cicloalquilo en los dos radicales antes mencionados son no sustituidos o parcial o totalmente halogenados; C₁₋₈-alcoxi, C₁₋₆-haloalcoxi, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₄-alcoxi-C₁₋₄-alquilo, C₁₋₄-alquil-S(O)ₙ-C₁₋₄-alquilo, C₁₋₄-alquilamino-C₁₋₄-alquilo, di-(C₁₋₄-alquil)-amino-C₁₋₄-alquilo, C₁₋₆-cianoalquilo, fenilo, bencilo y heterociclilo, en donde el heterociclilo es un heterociclo monocíclico de 5 ó 6 miembros saturado, parcialmente insaturado o aromático que contiene 1, 2, 3 ó 4 heteroátomos seleccionados del grupo que consiste en O, N y S como miembros del anillo, en donde fenilo, bencilo y heterociclilo son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; R³ᵈ se selecciona del grupo que consiste en hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₃₋₇-cicloalquil-C₁₋₄-alquilo, en donde los grupos C₃₋₇-cicloalquilo en los dos radicales antes mencionados son no sustituidos o parcial o totalmente halogenados; C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₄-alcoxi-C₁₋₄-alquilo, C₁₋₄-alquil-S(O)ₙ-C₁₋₄-alquilo, C₁₋₄-alquilamino-C₁₋₄-alquilo, di-(C₁₋₄-alquil)-amino-C₁₋₄-alquilo, C₁₋₆-cianoalquilo, fenilo y bencilo, en donde fenilo y bencilo son no sustituido o sustituidos con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; R³ᵉ y R³ᶠ se seleccionan, independientemente entre sí, del grupo que consiste en hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₃₋₇-cicloalquil-C₁₋₄-alquilo, en donde los grupos C₃₋₇-cicloalquilo en donde los dos radicales antes mencionados son no sustituidos o parcial o totalmente halogenados; C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₄-alcoxi-C₁₋₄-alquilo, fenilo y bencilo, en donde fenilo y bencilo son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; o R³ᵉ y R³ᶠ, junto con el átomo de nitrógeno al que están unidos, pueden formar un radical heterocíclico saturado o insaturado de 4, 5, 6 ó 7 miembros, que puede contener como miembro del anillo otro heteroátomo seleccionado del grupo que consiste en O, S y N y que es no sustituido, o puede tener 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en =O, halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; R³ᵍ y R³ʰ se selecciona, independientemente entre sí, del grupo que consiste en hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₇-cicloalquilo, C₃₋₇-cicloalquil-C₁₋₄-alquilo, en donde los grupos C₃₋₇-cicloalquilo en los dos radicales antes mencionados son no sustituidos o parcial o totalmente halogenados; C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₄-alcoxi-C₁₋₄-alquilo, C₁₋₄-alquilsulfonilo, un radical C(O)Rᵏ, fenilo y bencilo, en donde fenilo y bencilo son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; o R³ᵍ y R³ʰ, junto con el átomo de nitrógeno al que están unidos, pueden formar un radical heterocíclico saturado o insaturado de 4, 5, 6 ó 7 miembros, que puede contener como miembro del anillo otro heteroátomo seleccionado del grupo que consiste en O, S y N y que es no sustituido, o puede tener 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en =O, halógeno, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi y C₁₋₄-haloalcoxi; cada R²² se selecciona independientemente del grupo que consiste en hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquenilo, C₃₋₆-halocicloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alquilo, C₁₋₆-alcoxi-C₁₋₆-alquilo, C₃₋₆-cicloalquil-C₁₋₆-alcoxi-C₁₋₆-alquilo, fenil-Z¹, fenil-O-C₁₋₆-alquilo, fenil-N(R²³)-C₁₋₆-alquilo, fenil-S(O)ₙ-C₁₋₆-alquilo, heterociclil-Z¹, heterociclil-N(R²³)-C₁₋₆-alquilo, heterociclil-O-C₁₋₆-alquilo y heterociclil-S(O)ₙ-C₁₋₆-alquilo, en donde heterociclilo es un heterociclo saturado, parcialmente insaturado o aromático monocíclico de 5 ó 6 miembros, que contiene 1, 2, 3 ó 4 heteroátomos, que se seleccionan del grupo que consiste en O, N y S como miembros del anillo, en donde fenilo y heterociclilo son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos que son idénticos o diferentes y se seleccionan del grupo que consiste en ciano, halógeno, nitro, tiocianato, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₆-cicloalquilo, C(O)OR²³, C(O)N(R²³)₂, OR²³, N(R²³)₂, S(O)ₙR²⁴, S(O)₂OR²³, S(O)₂N(R²³)₂ y R²³O-C₁₋₆-alquilo, y en donde heterociclilo tiene 0, 1 ó 2 grupos oxo; cada R²³ se selecciona independientemente del grupo que consiste en hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alquilo y fenilo; R²⁴ se selecciona del grupo que consiste en C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alquilo, y fenilo; R²⁵ se selecciona del grupo que consiste en C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquenilo, C₃₋₆-halocicloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alquilo, C₁₋₆-alcoxi-C₁₋₆-alquilo, C₃₋₆-cicloalquil-C₁₋₆-alcoxi-C₁₋₆-alquilo, fenil-Z¹, fenil-O-C₁₋₆-alquilo, fenil-N(R²³)-C₁₋₆-alquilo, fenil-S(O)ₙ-C₁₋₆-alquilo, heterociclil-Z¹, heterociclil-N(R²³)-C₁₋₆-alquilo, heterociclil-O-C₁₋₆-alquilo y heterociclil-S(O)ₙ-C₁₋₆-alquilo, en donde heterociclilo es un heterociclo saturado, parcialmente insaturado o aromático monocíclico de 5 ó 6 miembros, que contiene 1, 2, 3 ó 4 heteroátomos, que se seleccionan del grupo que consiste en O, N y S como miembros del anillo, en donde fenilo y heterociclilo son no sustituidos o sustituidos con 1, 2, 3 ó 4 grupos, que son idénticos o diferentes y se seleccionan del grupo que consiste en ciano, halógeno, nitro, tiocianato, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₆-cicloalquilo, C(O)OR²³, C(O)N(R²³)₂, OR²³, N(R²³)₂, S(O)ₙR²⁴, S(O)ₙR²⁴, S(O)₂N(R²³)₂ y R²³O-C₁₋₆-alquilo, y en donde heterociclilo tiene 0, 1 ó 2 grupos oxo; Rᵏ independientemente tiene los significados de R³ᶜ; k es 0, 1 ó 2; y n es 0, 1 ó 2; o un N-óxido o una sal adecuada en la agricultura de aquel.Benzamide compounds of formula (1), wherein the variables are defined in the claims and the description, the N-oxides and their salts, and compositions comprising them. Also the use of benzamide compounds, or of compositions comprising such compounds to control unwanted vegetation, and a method of controlling unwanted vegetation by applying said compounds or compositions. Claim 1: A compound characterized by formula (1), where Q is a compound of formula Q¹ or Q² or Q³ or Q⁴, from the group of formulas (2), where # represents the point of attachment with the rest of the molecule; R¹ is selected from the group consisting of cyano, halogen, nitro, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₂₋₈-alkenyl, C₂₋₈-alkynyl, C₁₋₄-alkoxy-C₁₋₄-alkyl, C₁₋₄-haloalkoxy-C₁₋₄-alkyl, C₁₋₈-alkoxy, C₁₋₆-haloalkoxy, C₁₋₄-alkoxy-C₁₋₄-alkoxy-Z¹ and R¹ᵇ-S (O) ₖ-Z¹; R² is selected from the group consisting of phenyl-Z⁴-S (O) ₙ-Z², heterocyclyl-Z⁴-S (O) ₙ-Z², Cyc-Z⁴-S (O) ₙ-Z², and Het-Z²ᵃ, where the cyclic groups of the four aforementioned radicals are unsubstituted or substituted with 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, nitro, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylsulfonyl, phenyl, and oxo; wherein Cyc is C₃₋₆-cycloalkyl or C₃₋₆-cycloalkyl fused to a benzene ring; wherein the heterocyclyl is a 3, 4, 5, or 6-membered monocyclic or 7, 8, 9, or 10-membered bicyclic saturated, partially unsaturated, or fully unsaturated heterocycle containing 1, 2, 3, or 4 heteroatoms selected from the group consisting in O, N and S (O) ₙ as ring members; and wherein Het is a saturated 5- or 6-membered heterocycle containing 1 or 2 S (O) ₙ groups as ring members; R³ is selected from the group consisting of hydrogen, cyano, thiocyanate, halogen, nitro, hydroxy-Z³, C₁₋₈-alkyl, C₁₋₄-cyanoalkyl, C₁₋₈-haloalkyl, C₂₋₈-alkenyl, C₂₋₈- haloalkenyl, C₂₋₈-alkynyl, C₃₋₈-haloalkynyl, C₃₋₁₀-cycloalkyl-Z³, C₃₋₆-cycloalkenyl-Z³, C₃₋₁₀-cycloalkoxy-Z³, C₃₋₁₀-cycloalkyl-C₁₋₂-alkoxy, wherein the cyclic groups of the four aforementioned radicals are unsubstituted or partially or fully halogenated; C₁₋₈-alkoxy-Z³, C₁₋₈-haloalkoxy-Z³, C₁₋₄-alkoxy-C₁₋₄-alkoxy-Z³, C₁₋₄-haloalkoxy-C₁₋₄-alkoxy-Z³, C₂₋₈-alkenyloxy- Z³, C₂₋₈-haloalkenyloxy-Z³, C₂₋₈-alkynyloxy-Z³, C₃₋₈-haloalkynyloxy-Z³, R³ᵇ-S (O) ₖ-Z³, R³ᶜ-C (O) -Z³, R³ᵈO-C (O ) -Z³, R³ᵈO-N = CH-Z³, R³ᵉR³ᶠN-C (O) -Z³, R³ᵍR³ʰN-Z³, R²²C (O) O-Z³, R²⁵OC (O) O-Z³, (R²²) ₂NC (O) O- Z³, R²⁵S (O) ₂O-Z³, R²²OS (O) ₂-Z³, (R²²) ₂NS (O) ₂-Z³, R²⁵OC (O) N (R²²) -Z³, (R²²) ₂NC (O) N (R²² ) -Z³, (R²²) ₂NS (O) ₂N (R²²) -Z³, (OH) ₂P (O) -Z³, (C₁₋₄-alkoxy) ₂P (O) -Z³, phenyl-Z³ᵃ and heterocyclyl-Z³ᵃ, wherein the heterocyclyl is a 3-, 4-, 5- or 6-membered monocyclic or 8-, 9- or 10-membered bicyclic saturated, partially unsaturated, or aromatic heterocycle containing 1, 2, 3, or 4 heteroatoms selected from the group consisting of O, N and S as members of the ring; wherein the cyclic groups on phenyl-Z³ᵃ and heterocyclyl-Z³ᵃ are unsubstituted or substituted with 1, 2, 3, or 4 R²¹ groups that are identical or different; wherein R³ is not nitro if R² is phenyl-S (O) ₙ-Z² or C₃₋₆-cycloalkyl-S (O) ₙ-Z²; R⁴ is selected from the group consisting of hydrogen, halogen, nitro, cyano-Z¹, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₃₋₇-cycloalkyl-C₁₋₄-alkyl, where the C₃₋₇-cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or fully halogenated; C₂₋₈-alkenyl, C₂₋₈-alkynyl, C₁₋₃-alkylamino, di- (C₁₋₃-alkyl) -amino, C₁₋₃-alkylamino-S (O) ₖ, C₁₋₃-alkylcarbonyl, C₁₋ ₈-alkoxy, C₁₋₆-haloalkoxy, C₁₋₄-alkoxy-C₁₋₄-alkyl, C₁₋₄-haloalkoxy-C₁₋₄-alkyl, C₁₋₄-alkoxy-C₁₋₄-alkoxy-Z¹, C₁₋ ₄-haloalkoxy-C₁₋₄-alkoxy-Z¹, C₁₋₄-alkithio-C₁₋₄-alkylthio-Z¹, C₂₋₆-alkenyloxy, C₂₋₆-alkynyloxy, R¹ᵇ-S (O) ₖ-Z¹, phenoxy- Z¹ and heterocyclyloxy-Z¹, where heterocyclyloxy is a 5 or 6 membered monocyclic or 8, 9 or 10 membered saturated oxygen-bonded bicyclic heterocycle containing 1, 2, 3, or 4 heteroatoms selected from the group consisting of O, N and S as members of the ring; wherein the cyclic groups in phenoxy and heterocyclyloxy are unsubstituted or substituted with 1, 2, 3, or 4 R¹¹ groups that are identical or different; Each R⁵ is independently selected from the group consisting of C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₃₋₇-cycloalkyl-C₁₋₄-alkyl, wherein the C₃₋₇-cycloalkyl groups of the two aforementioned radicals are unsubstituted or partially or fully halogenated; C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₁₋₄-alkoxy-C₁₋₄-alkyl, C₁₋₄-haloalkoxy-C₁₋₄-alkyl, Rᵇ- S (O) ₙ-C₁₋₃-alkyl, phenyl and benzyl, wherein phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups that are identical or different and are selected from the group consisting of halogen, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy and C₁₋₄-haloalkoxy; wherein R⁵ is not C₁₋₄-alkoxy-C₁₋₄-alkyl if R² is C₃₋₆-cycloalkyl-S (O) ₙ-Z²; R¹¹ and R²¹ are independently selected from the group consisting of cyano, halogen, nitro, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₃₋₇-halocycloalkyl, C₂₋₆- alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-alkoxy-C₁₋₄-alkyl, C₁₋₄-haloalkoxy- C₁₋₄-alkyl, C₁₋₄-alkylthio-C₁₋₄-alkyl, C₁₋₄-alkoxy-C₁₋₄-alkoxy and C₃₋₇-cycloalkoxy, or two R²¹ radicals attached to the same heterocyclyl carbon atom together can form a group = O; Z¹ and Z³ are independently selected from the group consisting of a covalent bond and C₁₋₄-alkaniyl; Z² is C₁₋₃-alkaniyl that is unsubstituted or substituted with 1, 2, 3, or 4 groups that are identical or different and are selected from the group consisting of C₁₋₄-alkyl and C₁₋₄-haloalkyl; Z²ᵃ is a covalent bond or C₁₋₃-alkaniyl that is unsubstituted or substituted with 1, 2, 3 or 4 groups that are identical or different and are selected from the group consisting of C₁₋₄-alkyl and C₁₋₄-haloalkyl ; Z³ᵃ is selected from the group consisting of a covalent bond, C₁₋₄-alkaniyl, O-C₁₋₄-alkaniyl, C₁₋₄-alkaniyl-O, and C₁₋₄-alkaniyl-O-C₁₋₄-alkaliyl; Z⁴ is a covalent bond or C₁₋₃-alkaniyl; Rᵇ, R¹ᵇ, and R³ᵇ are independently selected from the group consisting of C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆ -alkynyl, C₃₋₆-haloalkynyl, phenyl and heterocyclyl, where heterocyclyl is a saturated, partially unsaturated or aromatic 5- or 6-membered monocyclic heterocycle containing 1, 2, 3, or 4 heteroatoms selected from the group consisting of O, N and S as ring members, wherein phenyl and heterocyclyl are unsubstituted or substituted with 1, 2, 3, or 4 groups that are identical or different and are selected from the group consisting of halogen, C₁₋₄-alkyl, C₁₋₄ -haloalkyl, C₁₋₄-alkoxy and C₁₋₄-haloalkoxy; R³ᶜ is selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₃₋₇-cycloalkyl-C₁₋₄-alkyl, wherein the C₃₋₇-cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or fully halogenated; C₁₋₈-alkoxy, C₁₋₆-haloalkoxy, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₁₋₄-alkoxy-C₁₋₄-alkyl, C₁₋ ₄-alkyl-S (O) ₙ-C₁₋₄-alkyl, C₁₋₄-alkylamino-C₁₋₄-alkyl, di- (C₁₋₄-alkyl) -amino-C₁₋₄-alkyl, C₁₋₆- cyanoalkyl, phenyl, benzyl, and heterocyclyl, wherein the heterocyclyl is a saturated, partially unsaturated, or aromatic 5- or 6-membered monocyclic heterocycle containing 1, 2, 3, or 4 heteroatoms selected from the group consisting of O, N, and S as members of the ring, where phenyl, benzyl, and heterocyclyl are unsubstituted or substituted with 1, 2, 3, or 4 groups that are identical or different and are selected from the group consisting of halogen, C₁₋₄-alkyl, C₁₋₄-haloalkyl , C₁₋₄-alkoxy and C₁₋₄-haloalkoxy; R³ᵈ is selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₃₋₇-cycloalkyl-C₁₋₄-alkyl, wherein the C₃₋₇-cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or fully halogenated; C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₁₋₄-alkoxy-C₁₋₄-alkyl, C₁₋₄-alkyl-S (O) ₙ-C₁₋ ₄-alkyl, C₁₋₄-alkylamino-C₁₋₄-alkyl, di- (C₁₋₄-alkyl) -amino-C₁₋₄-alkyl, C₁₋₆-cyanoalkyl, phenyl and benzyl, where phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups that are identical or different and are selected from the group consisting of halogen, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, and C₁₋₄- haloalkoxy; R³ᵉ and R³ᶠ are independently selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₃₋₇-cycloalkyl-C₁₋₄-alkyl, wherein the C₃₋₇-cycloalkyl groups in which the two aforementioned radicals are unsubstituted or partially or fully halogenated; C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₁₋₄-alkoxy-C₁₋₄-alkyl, phenyl, and benzyl, where phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups that are identical or different and selected from the group consisting of halogen, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, and C₁₋₄-haloalkoxy; or R³ᵉ and R³ᶠ, together with the nitrogen atom to which they are attached, may form a 4, 5, 6, or 7-membered saturated or unsaturated heterocyclic radical, which may contain as a ring member another heteroatom selected from the group consisting of O , S and N and which is unsubstituted, or may have 1, 2, 3 or 4 groups which are identical or different and are selected from the group consisting of = O, halogen, C₁₋₄-alkyl, C₁₋₄-haloalkyl , C₁₋₄-alkoxy and C₁₋₄-haloalkoxy; R³ᵍ and R³ʰ are independently selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₇-cycloalkyl, C₃₋₇-cycloalkyl-C₁₋₄-alkyl, wherein the C₃₋₇-cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or fully halogenated; C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₁₋₄-alkoxy-C₁₋₄-alkyl, C₁₋₄-alkylsulfonyl, a C (O) Rᵏ radical, phenyl and benzyl, where phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups that are identical or different and are selected from the group consisting of halogen, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy and C₁₋₄-haloalkoxy; or R³ᵍ and R³ʰ, together with the nitrogen atom to which they are attached, may form a 4, 5, 6, or 7-membered saturated or unsaturated heterocyclic radical, which may contain as a ring member another heteroatom selected from the group consisting of O , S and N and which is unsubstituted, or may have 1, 2, 3 or 4 groups which are identical or different and are selected from the group consisting of = O, halogen, C₁₋₄-alkyl, C₁₋₄-haloalkyl , C₁₋₄-alkoxy and C₁₋₄-haloalkoxy; each R²² is independently selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₃₋ ₆-cycloalkyl, C₃₋₆-cycloalkenyl, C₃₋₆-halocycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₁₋₆-alkyl, C₃₋₆-cycloalkyl-C₁₋₆- alkoxy-C₁₋₆-alkyl, phenyl-Z¹, phenyl-O-C₁₋₆-alkyl, phenyl-N (R²³) -C₁₋₆-alkyl, phenyl-S (O) ₙ-C₁₋₆-alkyl, heterocyclyl -Z¹, heterocyclyl-N (R²³) -C₁₋₆-alkyl, heterocyclyl-O-C₁₋₆-alkyl and heterocyclyl-S (O) ₙ-C₁₋₆-alkyl, where heterocyclyl is a saturated, partially unsaturated heterocycle or 5- or 6-membered monocyclic aromatic, containing 1, 2, 3, or 4 heteroatoms, which are selected from the group consisting of O, N, and S as ring members, wherein phenyl and heterocyclyl are unsubstituted or substituted with 1 , 2, 3 or 4 groups that are identical or different and are selected from the group consisting of cyano, halogen, nitro, thiocyanate, C₁₋₆-alkyl, C₁₋₆-h alloalkyl, C₃₋₆-cycloalkyl, C (O) OR²³, C (O) N (R²³) ₂, OR²³, N (R²³) ₂, S (O) ₙR²⁴, S (O) ₂OR²³, S (O) ₂N ( R²³) ₂ and R²³O-C₁₋₆-alkyl, and wherein heterocyclyl has 0, 1 or 2 oxo groups; each R²³ is independently selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋ ₆-alkyl and phenyl; R²⁴ is selected from the group consisting of C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, and phenyl; R²⁵ is selected from the group consisting of C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₃₋₆-haloalkynyl, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkenyl, C₃₋₆-halocycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₁₋₆-alkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkoxy-C₁₋ ₆-alkyl, phenyl-Z¹, phenyl-O-C₁₋₆-alkyl, phenyl-N (R²³) -C₁₋₆-alkyl, phenyl-S (O) ₙ-C₁₋₆-alkyl, heterocyclyl-Z¹, heterocyclyl -N (R²³) -C₁₋₆-alkyl, heterocyclyl-O-C₁₋₆-alkyl and heterocyclyl-S (O) ₙ-C₁₋₆-alkyl, where heterocyclyl is a saturated, partially unsaturated, or monocyclic aromatic heterocycle of 5 or 6-membered, containing 1, 2, 3, or 4 heteroatoms, which are selected from the group consisting of O, N, and S as ring members, wherein phenyl and heterocyclyl are unsubstituted or substituted with 1, 2, 3 or 4 groups, which are identical or different and selected from the group consisting of cyano, halogen, nitro, thiocyanate, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₃₋₆-cycloalkyl, C (O ) OR²³, C (O) N (R²³) ₂, OR²³, N (R²³) ₂, S (O) ₙR²⁴, S (O) ₙR²⁴, S (O) ₂N (R²³) ₂ and R²³O-C₁₋₆-alkyl , and wherein heterocyclyl has 0, 1 or 2 oxo groups; Rᵏ independently has the meanings of R³ᶜ; k is 0, 1 or 2; and n is 0, 1 or 2; or an N-oxide or a salt suitable in agriculture thereof.

ARP180103823A 2017-12-22 2018-12-21 BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES AR114040A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP17210287 2017-12-22

Publications (1)

Publication Number Publication Date
AR114040A1 true AR114040A1 (en) 2020-07-15

Family

ID=60811887

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP180103823A AR114040A1 (en) 2017-12-22 2018-12-21 BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES

Country Status (2)

Country Link
AR (1) AR114040A1 (en)
WO (1) WO2019122345A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB202106945D0 (en) * 2021-05-14 2021-06-30 Syngenta Crop Protection Ag Improvements in or relating to organic compounds
CN114015805A (en) * 2021-10-13 2022-02-08 四川农业大学 Fluorescent RT-RAA primer and kit for detecting Getavirus and application of fluorescent RT-RAA primer and kit

Family Cites Families (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5304732A (en) 1984-03-06 1994-04-19 Mgi Pharma, Inc. Herbicide resistance in plants
BR8600161A (en) 1985-01-18 1986-09-23 Plant Genetic Systems Nv CHEMICAL GENE, HYBRID, INTERMEDIATE PLASMIDIO VECTORS, PROCESS TO CONTROL INSECTS IN AGRICULTURE OR HORTICULTURE, INSECTICIDE COMPOSITION, PROCESS TO TRANSFORM PLANT CELLS TO EXPRESS A PLANTINIDE TOXIN, PRODUCED BY CULTURES, UNITED BY BACILLA
EP0242236B2 (en) 1986-03-11 1996-08-21 Plant Genetic Systems N.V. Plant cells resistant to glutamine synthetase inhibitors, made by genetic engineering
IL83348A (en) 1986-08-26 1995-12-08 Du Pont Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5013659A (en) 1987-07-27 1991-05-07 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
FR2629098B1 (en) 1988-03-23 1990-08-10 Rhone Poulenc Agrochimie CHEMICAL GENE OF HERBICIDE RESISTANCE
CA2005658A1 (en) 1988-12-19 1990-06-19 Eliahu Zlotkin Insecticidal toxins, genes encoding these toxins, antibodies binding to them and transgenic plant cells and plants expressing these toxins
DK0392225T3 (en) 1989-03-24 2003-09-22 Syngenta Participations Ag Disease resistant transgenic plants
ATE121267T1 (en) 1989-11-07 1995-05-15 Pioneer Hi Bred Int LARVAE-KILLING LECTINS AND BASED PLANT RESISTANCE AGAINST INSECTS.
EP0536330B1 (en) 1990-06-25 2002-02-27 Monsanto Technology LLC Glyphosate tolerant plants
UA48104C2 (en) 1991-10-04 2002-08-15 Новартіс Аг Dna fragment including sequence that codes an insecticide protein with optimization for corn, dna fragment providing directed preferable for the stem core expression of the structural gene of the plant related to it, dna fragment providing specific for the pollen expression of related to it structural gene in the plant, recombinant dna molecule, method for obtaining a coding sequence of the insecticide protein optimized for corn, method of corn plants protection at least against one pest insect
US5530195A (en) 1994-06-10 1996-06-25 Ciba-Geigy Corporation Bacillus thuringiensis gene encoding a toxin active against insects
DE19505995A1 (en) 1995-02-21 1996-08-22 Degussa Process for the preparation of thietanones
FR2734842B1 (en) 1995-06-02 1998-02-27 Rhone Poulenc Agrochimie DNA SEQUENCE OF A HYDROXY-PHENYL PYRUVATE DIOXYGENASE GENE AND OBTAINING PLANTS CONTAINING A HYDROXY-PHENYL PYRUVATE DIOXYGENASE GENE, TOLERANT TO CERTAIN HERBICIDES
AU1670997A (en) 1996-04-26 1997-11-19 Nippon Soda Co., Ltd. Novel benzene derivatives substituted by heterocycles and herbicides
CN1076351C (en) 1996-04-26 2001-12-19 日本曹达株式会社 Novel benzene derivatives substituted by heterocycles and herbicides
WO1997041116A1 (en) 1996-04-26 1997-11-06 Nippon Soda Co., Ltd. Benzene derivatives substituted by heterocycles and herbicides
US5773704A (en) 1996-04-29 1998-06-30 Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Herbicide resistant rice
CA2257196A1 (en) 1996-06-06 1997-12-11 Morris Padgett Rorer Herbicidal pyridinyl and pyrazolylphenyl ketones
US5773702A (en) 1996-07-17 1998-06-30 Board Of Trustees Operating Michigan State University Imidazolinone herbicide resistant sugar beet plants
JP3842299B2 (en) 1996-07-17 2006-11-08 ミシガン ステイト ユニバーシティー Sugar beet plant resistant to imidazolinone herbicide
CA2278331C (en) 1997-01-17 2008-11-18 Basf Aktiengesellschaft 3-heterocyclyl-substituted benzoyl derivatives
EP0966452B1 (en) 1997-01-17 2003-05-02 Basf Aktiengesellschaft Process for preparing sulphurous 2-chloro-3-(4,5-dihydroisoxazol-3-yl)-benzoic acids
EP1097925B1 (en) 1998-07-14 2006-09-13 Nippon Soda Co., Ltd. Novel benzoic acid derivatives and processes for the preparation thereof
US6348643B1 (en) 1998-10-29 2002-02-19 American Cyanamid Company DNA sequences encoding the arabidopsis acetohydroxy-acid synthase small subunit and methods of use
US6277847B1 (en) 1999-04-02 2001-08-21 Fmc Corporation Herbicidal isoindolinonyl-and 3,4-dihydroisoquinolonyl-substituted heterocycles
EP1284597A4 (en) 2000-04-28 2005-12-28 Basf Ag Use of the maize x112 mutant ahas 2 gene and imidazolinone herbicides for selection of transgenic monocots, maize, rice and wheat plants resistant to the imidazolinone herbicides
IL148464A0 (en) 2000-05-04 2002-09-12 Basf Ag Uracil substituted phenyl sulfamoyl carboxamides
US6768044B1 (en) 2000-05-10 2004-07-27 Bayer Cropscience Sa Chimeric hydroxyl-phenyl pyruvate dioxygenase, DNA sequence and method for obtaining plants containing such a gene, with herbicide tolerance
BR0113500A (en) 2000-08-25 2003-07-01 Syngenta Participations Ag Insecticidal toxins derived from bacillus thuringiensis insecticide crystal proteins
DE10043075A1 (en) 2000-09-01 2002-03-14 Aventis Cropscience Gmbh Heterocyclyl-substituted benzoylcyclohexanediones, process for their preparation and their use as herbicides
CA2808328C (en) 2001-08-09 2019-08-06 Northwest Plant Breeding Company Wheat plants having increased resistance to imidazolinone herbicides
ATE527363T1 (en) 2001-08-09 2011-10-15 Univ Saskatchewan WHEAT PLANTS WITH INCREASED RESISTANCE TO IMIDAZOLINONE HERBICIDES
AR036336A1 (en) 2001-08-09 2004-09-01 Univ Saskatchewan A WHEAT PLANT THAT INCLUDES NUCLEIC ACIDS, A PLANT PART, A PLANT CELL., A SEED PRODUCED BY THE PLANT, AN IMI ISOLATED NUCLEIC ACID, A METHOD FOR CONTROLLING THE WEEDS, A METHOD TO MODIFY THE TOLERANCE AND PLASTERS A METHOD TO PRODUCE A TRANSGE PLANT
US7230167B2 (en) 2001-08-31 2007-06-12 Syngenta Participations Ag Modified Cry3A toxins and nucleic acid sequences coding therefor
AR037856A1 (en) 2001-12-17 2004-12-09 Syngenta Participations Ag CORN EVENT
US7829762B2 (en) 2002-07-10 2010-11-09 Department Of Agriculture Wheat plants having increased resistance to imidazolinone herbicides
EP1633875B1 (en) 2003-05-28 2012-05-02 Basf Se Wheat plants having increased tolerance to imidazolinone herbicides
US20070028318A1 (en) 2003-08-29 2007-02-01 Instituto Nacional De Technologia Agropecuaria Rice plants having increased tolerance to imidazolinone herbicides
US7297541B2 (en) 2004-01-26 2007-11-20 Monsanto Technology Llc Genes encoding 4-hydroxyphenylpyruvate dioxygenase (HPPD) enzymes for plant metabolic engineering
CA2641389A1 (en) 2006-02-15 2007-08-23 F. Hoffmann-La Roche Ag Hetero-bycyclic antiviral compounds
GB0625598D0 (en) 2006-12-21 2007-01-31 Syngenta Ltd Novel herbicides
IN2012DN03057A (en) 2009-09-25 2015-07-31 Bayer Cropscience Ag
EA023205B9 (en) 2010-09-01 2016-09-30 Байер Интеллектуэль Проперти Гмбх N-(tetrazol-5-yl)- and n-(triazol-5-yl)arylcarboxamides and herbicide
CA2830773C (en) 2011-03-22 2021-01-26 Arnim Kohn N-(1,3,4-oxadiazol-2-yl)arylcarboxamides and use thereof as herbicides
ES2542681T3 (en) 2011-08-03 2015-08-10 Bayer Intellectual Property Gmbh N- (tetrazol-5-yl) - and N- (triazol-5-yl) arylcarboxylic acid amides and their use as herbicides
EP2589598A1 (en) 2011-11-03 2013-05-08 Bayer CropScience AG 5-phenyl substituted N-(Tetrazol-5-yl)- and N-(Triazol-5-yl)aryl carboxylic acid amides and use of same as herbicides
US9169219B2 (en) 2012-02-21 2015-10-27 Bayer Intellectual Property Gmbh Herbicidally active 4-nitro-substituted N-(tetrazol-5-yl)-, N-(triazol-5-yl)-, and N-(1,3,4-0XADIAZOL-2-yl)aryl carboxylic acid amides
US9867376B2 (en) 2012-05-24 2018-01-16 Bayer Cropscience Ag Herbicidal compositions comprising N-tetrazol-5-yl)- or N-(triazol-5-yl)arylcarboxamides

Also Published As

Publication number Publication date
WO2019122345A1 (en) 2019-06-27

Similar Documents

Publication Publication Date Title
AR100315A1 (en) PIRIDINE SUBSTITUTED COMPOUNDS THAT HAVE HERBICITY ACTION
AR108557A1 (en) HERBICIDE URACILPIRIDINS
AR088886A1 (en) 1,2,5-OXADIAZOL SUBSTITUTED COMPOUNDS AND ITS USE AS HERBICIDES II
AR104487A1 (en) QUINOLINE COMPOUNDS
AR106763A1 (en) OXADIAZOLS REPLACED TO FIGHT FITOPATHOGEN FUNGI
AR105456A1 (en) PIRIDINE COMPOUNDS WITH FUNGICIDE ACTION
AR100171A1 (en) DIAMINOTRIAZINE COMPOUNDS AND ITS USE AS A HERBICIDE
AR113905A1 (en) HERBICIDE PHENYLETERS
AR106873A1 (en) PIRIDINE COMPOUNDS AS FUNGICIDES
AR095110A1 (en) METHOD FOR CONTROLLING PESTS
AR113842A1 (en) THIAZOL DERIVATIVES MICROBIOCIDES
AR107738A1 (en) ACID AMIDES N- (5-HALOGEN-1,3,4-OXADIAZOL-2-IL) ARYLBARBOXYL AND ITS USE AS HERBICIDES
AR109152A1 (en) HERBICIDE PIRIMIDINE COMPOUNDS
AR106872A1 (en) PIRIDINE COMPOUNDS AS FUNGICIDES
AR107955A1 (en) DERIVATIVES OF PIRIDINO- / PIRIMIDINO-PIRIDINA, WITH HERBICITY ACTIVITY
AR114040A1 (en) BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES
AR100706A1 (en) NAFTIRIDINADIONA DERIVATIVES
AR096827A1 (en) USE OF SELECTED PYRIDONCARBOXAMIDS OR ITS SALTS AS ACTIVE INGREDIENTS AGAINST ABIOTIC STRESS IN PLANTS
AR119397A1 (en) HERBICIDE COMPOUNDS
AR114176A1 (en) BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES
AR120426A1 (en) INDOL, INDAZOLE AND BENZOTRIAZOLE DERIVATIVES WITH HERBICIDAL ACTIVITY
AR112112A1 (en) BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES
AR095146A1 (en) VEGETAL GROWTH REGULATING COMPOUNDS
AR089878A1 (en) PIRIMIDINE FUNGICIDE COMPOUNDS I
AR114048A1 (en) SILILMETIL HETEROARYLLOXYQUINOLINES TRISUSTITUIDAS AND THEIR ANALOGUES

Legal Events

Date Code Title Description
FB Suspension of granting procedure