AR109572A1 - COMBINATIONS OF ACTIVE COMPOUNDS - Google Patents

COMBINATIONS OF ACTIVE COMPOUNDS

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Publication number
AR109572A1
AR109572A1 ARP170102454A ARP170102454A AR109572A1 AR 109572 A1 AR109572 A1 AR 109572A1 AR P170102454 A ARP170102454 A AR P170102454A AR P170102454 A ARP170102454 A AR P170102454A AR 109572 A1 AR109572 A1 AR 109572A1
Authority
AR
Argentina
Prior art keywords
methyl
tetrazol
phenyl
oxymethyl
pyrazol
Prior art date
Application number
ARP170102454A
Other languages
Spanish (es)
Inventor
Wachendorff-Neumann Ulrike Dr
Ruth Meissner
Christophe Dubost
Grtz Andreas Dr
Maechling Simon Dr
Original Assignee
Bayer Cropscience Ag
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 Bayer Cropscience Ag filed Critical Bayer Cropscience Ag
Publication of AR109572A1 publication Critical patent/AR109572A1/en

Links

Classifications

    • 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
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Abstract

Reivindicación 1: Combinaciones que comprenden: (A) al menos uno de fórmula (1), donde X¹, X² representan independientemente H, halógeno, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₁₋₈-alquiloxi, C₁₋₈-alquilsulfanilo, ciano; R¹ representa H, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₃₋₈-cicloalquilo, C₃₋₈-halocicloalquilo, C₁₋₄-alquil-C₃₋₈-cicloalquilo; C₁₋₄-alquil-C₃₋₈-halocicloalquilo; R², R³ representan independientemente H, C₁₋₈-alquilo, C₁₋₈-haloalquilo, C₃₋₈-cicloalquilo, C₃₋₈-halocicloalquilo, C₁₋₄-alquil-C₃₋₈-cicloalquilo; C₁₋₄-alquil-C₃₋₈-halocicloalquilo; o una sal agroquímicamente aceptable de estos, y (B) al menos otro compuesto activo adicional seleccionado de los siguientes grupos: (1.1) ipfentrifluconazol, (1.2) (2E,3Z)-5-{[1-(4-cloro-2-fluorofenil)-1H-pirazol-3-il]oxi}-2-(metoxiimino)-N,3-dimetilpent-3-enamida, (1.3) 1-[3-cloro-2-[[1-(4-clorofenil)pirazol-3-il]oximetil]fenil]-4-metil-tetrazol-5-ona, (1.4) 1-[3-bromo-2-[[1-(4-clorofenil)pirazol-3-il]oximetil]fenil]-4-metil-tetrazol-5-ona, (1.5) 1-[2-[[1-(4-clorofenil)pirazol-3-il]oximetil]-3-metil-fenil]-4-metil-tetrazol-5-ona, (1.6) 1-[2-[[1-(4-clorofenil)pirazol-3-il]oximetil]-3-fluoro-fenil]-4-metil-tetrazol-5-ona, (1.7) 1-[2-[[1-(2,4-diclorofenil)pirazol-3-il]oximetil]-3-fluorofenil]-4-metil-tetrazol-5-ona, (1.8) 1-[2-[[4-(4-clorofenil)tiazol-2-il]oximetil]-3-metil-fenil]-4-metil-tetrazol-5-ona, (1.9) 1-[3-cloro-2-[[4-(p-tolil)tiazol-2-il]oximetil]fenil]-4-metil-tetrazol-5-ona, (1.10) 1-[3-ciclopropil-2-[[2-metil-4-(1-metilpirazol-3-il)fenoxi]metil]fenil]-4-metil-tetrazol-5-ona, (1.11) 1-[3-(difluorometoxi)-2-[[2-metil-4-(1-metilpirazol-3-il)fenoxi]metil]fenil]-4-metil-tetrazol-5-ona, (1.12) 1-metil-4-[3-metil-2-[[2-metil-4-(1-metilpirazol-3-il)fenoxi]metil]fenil]tetrazol-5-ona, (1.13) 1-metil-4-[3-metil-2-[[1-[3-(trifluorometil)fenil]etilideneamino]oximetil]fenil]tetrazol-5-ona, (1.14) 1-[3-cloro-2-[[1-(4-clorofenil)pirazol-3-il]oximetil]fenil]-4-metil-tetrazol-5-ona, (1.15) 6-etil-5,7-dioxo-6,7-dihidro-5H-pirrolo[3’,4’:5,6][1,4]ditiino[2,3-c][1,2]tiazol-3-carbonitrilo. Reivindicación 3: Combinaciones de acuerdo con la reivindicación 1 que comprenden al menos un compuesto de fórmula (1) seleccionado del grupo que consiste en los compuestos de las fórmulas (2) a (13). Reivindicación 4: Un método para controlar hongos fitopatógenos dañinos, caracterizado porque las combinaciones de acuerdo con la reivindicación 1 a 3 se aplican al hongo fitopatógeno dañino y/o su hábitat. Reivindicación 6: El uso de las combinaciones de acuerdo con las reivindicaciones 1 a 3 o composiciones de acuerdo con la reivindicación 5, para el control de hongos fitopatógenos dañinos. Reivindicación 7: Un proceso para producir composiciones para controlar hongos fitopatógenos dañinos, caracterizado porque las combinaciones de acuerdo con las reivindicaciones 1 a 3 se mezclan con extensores y/o tensioactivos.Claim 1: Combinations comprising: (A) at least one of formula (1), where X¹, X² independently represent H, halogen, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₁₋₈-alkyloxy, C₁₋₈ -alkylsulfanyl, cyano; R¹ represents H, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₃₋₈-cycloalkyl, C₃₋₈-halocycloalkyl, C₁₋₄-alkyl-C₃₋₈-cycloalkyl; C₁₋₄-alkyl-C₃₋₈-halocycloalkyl; R², R³ independently represent H, C₁₋₈-alkyl, C₁₋₈-haloalkyl, C₃₋₈-cycloalkyl, C₃₋₈-halocycloalkyl, C₁₋₄-alkyl-C₃₋₈-cycloalkyl; C₁₋₄-alkyl-C₃₋₈-halocycloalkyl; or an agrochemically acceptable salt thereof, and (B) at least one other additional active compound selected from the following groups: (1.1) ipfentrifluconazole, (1.2) (2E,3Z)-5-{[1-(4-chloro-2 -fluorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide, (1.3) 1-[3-chloro-2-[[1-(4- chlorophenyl)pyrazol-3-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one, (1.4) 1-[3-bromo-2-[[1-(4-chlorophenyl)pyrazol-3-yl] oxymethyl]phenyl]-4-methyl-tetrazol-5-one, (1.5) 1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-methyl-phenyl]-4- methyl-tetrazol-5-one, (1.6) 1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-fluoro-phenyl]-4-methyl-tetrazol-5-one , (1.7) 1-[2-[[1-(2,4-dichlorophenyl)pyrazol-3-yl]oxymethyl]-3-fluorophenyl]-4-methyl-tetrazol-5-one, (1.8) 1-[ 2-[[4-(4-chlorophenyl)thiazol-2-yl]oxymethyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one, (1.9) 1-[3-chloro-2-[ [4-(p-tolyl)thiazol-2-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one, (1.10) 1-[3-cyclopropyl-2-[[2-methyl-4-( 1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]-4-methyl-tetrazol-5-one , (1.11) 1-[3-(difluoromethoxy)-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]-4-methyl-tetrazol-5-one, ( 1.12) 1-methyl-4-[3-methyl-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]tetrazol-5-one, (1.13) 1-methyl -4-[3-methyl-2-[[1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]tetrazol-5-one, (1.14) 1-[3-chloro-2-[[1- (4-chlorophenyl)pyrazol-3-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one, (1.15) 6-ethyl-5,7-dioxo-6,7-dihydro-5H-pyrrolo[3 ’,4’:5.6][1,4]dithiino[2,3-c][1,2]thiazole-3-carbonitrile. Claim 3: Combinations according to claim 1 comprising at least one compound of formula (1) selected from the group consisting of compounds of formulas (2) to (13). Claim 4: A method for controlling harmful phytopathogenic fungi, characterized in that the combinations according to claim 1 to 3 are applied to the harmful phytopathogenic fungus and/or its habitat. Claim 6: The use of the combinations according to claims 1 to 3 or compositions according to claim 5, for the control of harmful phytopathogenic fungi. Claim 7: A process for producing compositions to control harmful phytopathogenic fungi, characterized in that the combinations according to claims 1 to 3 are mixed with extenders and/or surfactants.

ARP170102454A 2016-09-06 2017-09-04 COMBINATIONS OF ACTIVE COMPOUNDS AR109572A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP16187367 2016-09-06

Publications (1)

Publication Number Publication Date
AR109572A1 true AR109572A1 (en) 2018-12-26

Family

ID=56876966

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP170102454A AR109572A1 (en) 2016-09-06 2017-09-04 COMBINATIONS OF ACTIVE COMPOUNDS

Country Status (3)

Country Link
AR (1) AR109572A1 (en)
UY (1) UY37397A (en)
WO (1) WO2018046431A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020169414A1 (en) 2019-02-20 2020-08-27 Basf Se Pesticidal mixtures comprising a pyrazole compound
WO2020207870A1 (en) 2019-04-12 2020-10-15 Basf Se Pesticidal mixtures

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA027009B1 (en) 2012-12-19 2017-06-30 Байер Кропсайенс Акциенгезельшафт Difluoromethyl-nicotinic indanyl carboxamides
CA2918709C (en) * 2013-07-22 2021-07-13 Sumitomo Chemical Company, Limited Plant fungal disease control composition and its use
CR20170268A (en) * 2014-12-19 2018-01-25 Bayer Cropscience Ag COMBINATIONS OF ACTIVE COMPOUNDS
MX2017008144A (en) * 2014-12-19 2017-09-18 Bayer Cropscience Ag Active compound combinations.
AR102957A1 (en) * 2014-12-19 2017-04-05 Bayer Cropscience Ag COMBINATIONS OF ACTIVE COMPOUNDS

Also Published As

Publication number Publication date
WO2018046431A1 (en) 2018-03-15
UY37397A (en) 2018-03-23

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