AR093828A1 - Mezclas activas como plaguicidas, que comprenden compuestos de antranilamida - Google Patents
Mezclas activas como plaguicidas, que comprenden compuestos de antranilamidaInfo
- Publication number
- AR093828A1 AR093828A1 ARP130103520A ARP130103520A AR093828A1 AR 093828 A1 AR093828 A1 AR 093828A1 AR P130103520 A ARP130103520 A AR P130103520A AR P130103520 A ARP130103520 A AR P130103520A AR 093828 A1 AR093828 A1 AR 093828A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkoxy
- alkyl
- group
- radicals
- partially
- Prior art date
Links
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
También métodos y el uso de estas mezclas para combatir y controlar insectos, acáridos o nematodos y hongos dañinos en las plantas, y para proteger estas plantas contra la infestación por plagas, en especial, también para proteger el material de propagación vegetal, como las semillas. Reivindicación 1: Mezclas plaguicidas caracterizadas porque comprenden como compuestos activos i) al menos un compuesto de antranilamida activo como plaguicida de la fórmula (1), en donde R¹ se selecciona del grupo que consiste en halógeno, metilo y halometilo; R² se selecciona del grupo que consiste en hidrógeno, halógeno, halometilo y ciano; R³ se selecciona de hidrógeno, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquinilo C₂₋₆, haloalquinilo C₂₋₆, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈, alcoxi C₁₋₄-alquilo C₁₋₄, haloalcoxi C₁₋₄-alquilo C₁₋₄; C(=O)Rᵃ, C(=O)ORᵇ y C(=O)NRᶜRᵈ; R⁴ es hidrógeno o halógeno; R⁵, R⁶ se seleccionan, independientemente entre sí, del grupo que consiste en hidrógeno, alquilo C₁₋₁₀, cicloalquilo C₃₋₈, alquenilo C₂₋₁₀, alquinilo C₂₋₁₀, en donde los radicales alifáticos y cicloalifáticos antes mencionados se pueden sustituir con 1 a 10 sustituyentes Rᵉ, y fenilo, que es no sustituido o tiene de 1 a 5 sustituyentes Rᶠ; o R⁵ y R⁶ juntos representan cadenas de alquileno C₂₋₇, alquenileno C₂₋₇ o alquinileno C₆₋₉ que forman, junto con el átomo de azufre al que están unidas, un anillo saturado, parcialmente insaturado o totalmente insaturado de 3, 4, 5, 6, 7, 8, 9 ó 10 miembros, en donde de 1 a 4 de los grupos CH₂ en la cadena de alquileno C₂₋₇, de 1 a 4 de cualquiera de los grupos CH₂ o CH en la cadena de alquenileno C₂₋₇, o de 1 a 4 de cualquiera de los grupos CH₂ en la cadena de alquinileno C₆₋₉ se pueden reemplazar por 1 a 4 grupos seleccionados independientemente del grupo que consiste en C=O, C=S, O, S, N, NO, SO, SO₂ y NH, y en donde los átomos de carbono y/o nitrógeno en las cadenas de alquileno C₂₋₇, alquenileno C₂₋₇ o alquinileno C₆₋₉ se pueden sustituir con 1 a 5 sustituyentes seleccionados independientemente del grupo que consiste en halógeno, ciano, alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquiltio C₁₋₆, haloalquiltio C₁₋₆, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈, alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquinilo C₂₋₆ y haloalquinilo C₂₋₆; estos sustituyentes son idénticos o diferentes entre sí si hay más de un sustituyente presente; R⁷ se selecciona del grupo que consiste en bromo, cloro, difluorometilo, trifluorometilo, nitro, ciano, OCH₃, OCHF₂, OCH₂F, OCH₂CF₃, S(O)ₙCH₃ y S(=O)ₙCF₃; Rᵃ se selecciona del grupo que consiste en alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, alcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, parcial o totalmente halogenadas y/o pueden tener 1 ó 2 sustituyentes seleccionados de alcoxi C₁₋₄; fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆, (alcoxi C₁₋₆)carbonilo, alquilamino C₁₋₆ y di-(alquil C₁₋₆)amino; Rᵇ se selecciona del grupo que consiste en alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, alcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, parcial o totalmente halogenadas y/o pueden tener 1 ó 2 sustituyentes seleccionados de alcoxi C₁₋₄; fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆ y (alcoxi C₁₋₆)carbonilo; Rᶜ, Rᵈ se seleccionan, independientemente entre sí e independientemente de cada caso, del grupo que consiste en hidrógeno, ciano, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, parcial o totalmente halogenadas y/o pueden tener 1 ó 2 radicales seleccionados de alcoxi C₁₋₄; alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, haloalquiltio C₁₋₆, fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales mencionados pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆ y (alcoxi C₁₋₆)carbonilo; o Rᶜ y Rᵈ, junto con el átomo de nitrógeno al que están unidos, pueden formar un anillo heterocíclico saturado, parcialmente insaturado o totalmente insaturado de 3, 4, 5, 6 o 7 miembros, que también puede contener 1 ó 2 heteroátomos o grupos de heteroátomos adicionales seleccionados de N, O, S, NO, SO y SO₂, como miembros del anillo, en donde el anillo heterocíclico se puede sustituir opcionalmente con halógeno, haloalquilo C₁₋₄, alcoxi C₁₋₄ o haloalcoxi C₁₋₄; Rᵉ se selecciona independientemente del grupo que consiste en halógeno, ciano, nitro, -OH, -SH, -SCN, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, pueden ser parcial o totalmente halogenadas y/o pueden tener 1 ó 2 radicales seleccionados de alcoxi C₁₋₄; alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, haloalquiltio C₁₋₆, -ORᵃ, -NRᶜRᵈ, -S(O)ₙRᵃ, -S(O)ₙNRᶜRᵈ, -C(=O)Rᵃ, -C(=O)NRᶜRᵈ, -C(=O)ORᵇ, -C(=S)Rᵃ, -C(=S)NRᶜRᵈ, -C(=S)ORᵇ, -C(=S)SRᵇ, -C(=NRᶜ)Rᵇ, -C(=NRᶜ)NRᶜRᵈ, fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales mencionados pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆ y haloalcoxi C₁₋₆; o dos radicales vecinos Rᵉ forman juntos un grupo =O, =CH(alquilo C₁₋₄), =C(alquil C₁₋₄)alquilo C₁₋₄, =N(alquilo C₁₋₆) o =NO(alquilo C₁₋₆); Rᶠ se selecciona independientemente del grupo que consiste en halógeno, ciano, nitro, -OH, -SH, -SCN, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, pueden ser parcial o totalmente halogenadas y/o pueden tener 1 ó 2 radicales seleccionados de alcoxi C₁₋₄; alcoxi C₁₋₆, haloal
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201261708061P | 2012-10-01 | 2012-10-01 | |
US201361763974P | 2013-02-13 | 2013-02-13 | |
US201361847587P | 2013-07-18 | 2013-07-18 |
Publications (1)
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AR093828A1 true AR093828A1 (es) | 2015-06-24 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP130103520A AR093828A1 (es) | 2012-10-01 | 2013-09-27 | Mezclas activas como plaguicidas, que comprenden compuestos de antranilamida |
Country Status (11)
Country | Link |
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US (1) | US20150250173A1 (es) |
EP (1) | EP2903442A1 (es) |
JP (1) | JP2015530414A (es) |
KR (1) | KR20150067269A (es) |
CN (1) | CN104768377A (es) |
AR (1) | AR093828A1 (es) |
AU (1) | AU2013326645A1 (es) |
BR (1) | BR112015005094A2 (es) |
CR (1) | CR20150222A (es) |
MX (1) | MX2015004169A (es) |
WO (1) | WO2014053405A1 (es) |
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AR093243A1 (es) * | 2012-10-01 | 2015-05-27 | Basf Se | Uso de compuestos de n-tio-antranilamida en plantas cultivadas |
RU2658997C2 (ru) | 2012-11-22 | 2018-06-26 | Басф Корпорейшн | Пестицидные смеси |
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US10905122B2 (en) | 2016-03-16 | 2021-02-02 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on cereals |
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-
2013
- 2013-09-27 BR BR112015005094A patent/BR112015005094A2/pt not_active IP Right Cessation
- 2013-09-27 JP JP2015533602A patent/JP2015530414A/ja not_active Withdrawn
- 2013-09-27 US US14/432,044 patent/US20150250173A1/en not_active Abandoned
- 2013-09-27 WO PCT/EP2013/070160 patent/WO2014053405A1/en active Application Filing
- 2013-09-27 AR ARP130103520A patent/AR093828A1/es unknown
- 2013-09-27 EP EP13774629.3A patent/EP2903442A1/en not_active Withdrawn
- 2013-09-27 AU AU2013326645A patent/AU2013326645A1/en not_active Abandoned
- 2013-09-27 MX MX2015004169A patent/MX2015004169A/es unknown
- 2013-09-27 CN CN201380051204.1A patent/CN104768377A/zh active Pending
- 2013-09-27 KR KR1020157011488A patent/KR20150067269A/ko not_active Application Discontinuation
-
2015
- 2015-04-29 CR CR20150222A patent/CR20150222A/es unknown
Also Published As
Publication number | Publication date |
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CR20150222A (es) | 2015-09-16 |
CN104768377A (zh) | 2015-07-08 |
WO2014053405A1 (en) | 2014-04-10 |
US20150250173A1 (en) | 2015-09-10 |
JP2015530414A (ja) | 2015-10-15 |
AU2013326645A1 (en) | 2015-04-23 |
BR112015005094A2 (pt) | 2017-07-04 |
KR20150067269A (ko) | 2015-06-17 |
EP2903442A1 (en) | 2015-08-12 |
MX2015004169A (es) | 2015-10-22 |
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