AR109572A1 - COMBINATIONS OF ACTIVE COMPOUNDS - Google Patents
COMBINATIONS OF ACTIVE COMPOUNDSInfo
- 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
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 241000233866 Fungi Species 0.000 abstract 4
- 230000003032 phytopathogenic effect Effects 0.000 abstract 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 3
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- LSKRNXDVFOWBLH-UHFFFAOYSA-N 1-[3-chloro-2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]phenyl]-4-methyltetrazol-5-one Chemical compound O=C1N(C)N=NN1C1=CC=CC(Cl)=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 LSKRNXDVFOWBLH-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- SSZGPYLZHHCYJC-UHFFFAOYSA-N 1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-fluorophenyl]-4-methyltetrazol-5-one Chemical compound O=C1N(C)N=NN1C1=CC=CC(F)=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 SSZGPYLZHHCYJC-UHFFFAOYSA-N 0.000 abstract 1
- CCZNNOPONAPVCR-UHFFFAOYSA-N 1-[3-bromo-2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]phenyl]-4-methyltetrazol-5-one Chemical compound O=C1N(C)N=NN1C1=CC=CC(Br)=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 CCZNNOPONAPVCR-UHFFFAOYSA-N 0.000 abstract 1
- JCQPDMJQHYJDSS-UHFFFAOYSA-N 1-methyl-4-[3-methyl-2-[[1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]tetrazol-5-one Chemical compound CN1N=NN(C1=O)C1=C(C(=CC=C1)C)CON=C(C)C1=CC(=CC=C1)C(F)(F)F JCQPDMJQHYJDSS-UHFFFAOYSA-N 0.000 abstract 1
- VHVCMKPRANXWKQ-UHFFFAOYSA-N 1-methyl-4-[3-methyl-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]tetrazol-5-one Chemical compound CN1N=NN(C1=O)C1=C(C(=CC=C1)C)COC1=C(C=C(C=C1)C1=NN(C=C1)C)C VHVCMKPRANXWKQ-UHFFFAOYSA-N 0.000 abstract 1
- SIIJJFOXEOHODQ-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(C(F)(F)F)C=1C(O)(C(C)C)CN1C=NC=N1 SIIJJFOXEOHODQ-UHFFFAOYSA-N 0.000 abstract 1
- GYDLUVSMRCNDTQ-UHFFFAOYSA-N Cc1cc(ccc1OCc1c(cccc1-n1nnn(C)c1=O)C1CC1)-c1ccn(C)n1 Chemical compound Cc1cc(ccc1OCc1c(cccc1-n1nnn(C)c1=O)C1CC1)-c1ccn(C)n1 GYDLUVSMRCNDTQ-UHFFFAOYSA-N 0.000 abstract 1
- PYMSONKRELFQSE-UHFFFAOYSA-N Cc1cccc(c1COc1nc(cs1)-c1ccc(Cl)cc1)-n1nnn(C)c1=O Chemical compound Cc1cccc(c1COc1nc(cs1)-c1ccc(Cl)cc1)-n1nnn(C)c1=O PYMSONKRELFQSE-UHFFFAOYSA-N 0.000 abstract 1
- GVUOBBKPMNKLHO-UHFFFAOYSA-N ClC=1C(=C(C=CC1)N1N=NN(C1=O)C)COC=1SC=C(N1)C1=CC=C(C=C1)C Chemical compound ClC=1C(=C(C=CC1)N1N=NN(C1=O)C)COC=1SC=C(N1)C1=CC=C(C=C1)C GVUOBBKPMNKLHO-UHFFFAOYSA-N 0.000 abstract 1
- JSPNFPTTXLDNGF-UHFFFAOYSA-N Cn1nnn(-c2cccc(F)c2COc2ccn(n2)-c2ccc(Cl)cc2Cl)c1=O Chemical compound Cn1nnn(-c2cccc(F)c2COc2ccn(n2)-c2ccc(Cl)cc2Cl)c1=O JSPNFPTTXLDNGF-UHFFFAOYSA-N 0.000 abstract 1
- OTDPWLGCOBLOJJ-UHFFFAOYSA-N FC(OC=1C(=C(C=CC1)N1N=NN(C1=O)C)COC1=C(C=C(C=C1)C1=NN(C=C1)C)C)F Chemical compound FC(OC=1C(=C(C=CC1)N1N=NN(C1=O)C)COC1=C(C=C(C=C1)C1=NN(C=C1)C)C)F OTDPWLGCOBLOJJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004606 Fillers/Extenders Substances 0.000 abstract 1
- NFDFZNRAOQQYRF-UHFFFAOYSA-N [1,4]dithiino[2,3-c][1,2]thiazole-3-carbonitrile Chemical compound N#CC1=C2SC=CSC2=NS1 NFDFZNRAOQQYRF-UHFFFAOYSA-N 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- XUQQRGKFXLAPNV-UHFFFAOYSA-N metyltetraprole Chemical compound CC1=CC=CC(N2C(N(C)N=N2)=O)=C1COC(=N1)C=CN1C1=CC=C(Cl)C=C1 XUQQRGKFXLAPNV-UHFFFAOYSA-N 0.000 abstract 1
- LOWVXZYADKTOKN-QFWIXSRNSA-N n1c(OC\C=C(\C)/C(=N\OC)/C(=O)NC)ccn1-c1ccc(Cl)cc1F Chemical compound n1c(OC\C=C(\C)/C(=N\OC)/C(=O)NC)ccn1-c1ccc(Cl)cc1F LOWVXZYADKTOKN-QFWIXSRNSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
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
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
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.
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)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210131350A (en) | 2019-02-20 | 2021-11-02 | 바스프 에스이 | Pesticide Mixtures Containing Pyrazole Compounds |
| WO2020207870A1 (en) | 2019-04-12 | 2020-10-15 | Basf Se | Pesticidal mixtures |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6393273B2 (en) | 2012-12-19 | 2018-09-19 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | Difluoromethyl-nicotinic acid-indanyl carboxamides as fungicides |
| CN105555139A (en) * | 2013-07-22 | 2016-05-04 | 住友化学株式会社 | Plant disease control composition and use thereof |
| AR102957A1 (en) * | 2014-12-19 | 2017-04-05 | Bayer Cropscience Ag | COMBINATIONS OF ACTIVE COMPOUNDS |
| EA031300B1 (en) * | 2014-12-19 | 2018-12-28 | Байер Кропсайенс Акциенгезельшафт | Active compound combinations |
| CN107257625A (en) * | 2014-12-19 | 2017-10-17 | 拜耳作物科学股份公司 | Active agent combinations |
-
2017
- 2017-09-04 AR ARP170102454A patent/AR109572A1/en unknown
- 2017-09-04 WO PCT/EP2017/072075 patent/WO2018046431A1/en not_active Ceased
- 2017-09-06 UY UY0001037397A patent/UY37397A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| UY37397A (en) | 2018-03-23 |
| WO2018046431A1 (en) | 2018-03-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |