AR100048A1 - Composiciones herbicidas que comprenden isoxasolo[5,4-b]piridinas - Google Patents
Composiciones herbicidas que comprenden isoxasolo[5,4-b]piridinasInfo
- Publication number
- AR100048A1 AR100048A1 ARP150101076A ARP150101076A AR100048A1 AR 100048 A1 AR100048 A1 AR 100048A1 AR P150101076 A ARP150101076 A AR P150101076A AR P150101076 A ARP150101076 A AR P150101076A AR 100048 A1 AR100048 A1 AR 100048A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- inhibitors
- methyl
- trinoclane
- flamprop
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 6
- 239000000203 mixture Substances 0.000 title abstract 4
- 230000002363 herbicidal effect Effects 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 abstract 10
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 8
- -1 C3−6-halocycloalkyl Chemical group 0.000 abstract 5
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- GXEKYRXVRROBEV-FBXFSONDSA-N (1r,2s,3r,4s)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1C[C@@H]2[C@@H](C(O)=O)[C@@H](C(=O)O)[C@H]1O2 GXEKYRXVRROBEV-FBXFSONDSA-N 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 1
- LRKLFZPYIDPEHV-UHFFFAOYSA-N 1-methyl-2-[(2-methylphenyl)methoxymethyl]benzene Chemical compound CC1=CC=CC=C1COCC1=CC=CC=C1C LRKLFZPYIDPEHV-UHFFFAOYSA-N 0.000 abstract 1
- SVOAUHHKPGKPQK-UHFFFAOYSA-N 2-chloro-9-hydroxyfluorene-9-carboxylic acid Chemical compound C1=C(Cl)C=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 SVOAUHHKPGKPQK-UHFFFAOYSA-N 0.000 abstract 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 1
- OPEJGICLTMWFNQ-UHFFFAOYSA-N 5-[(2,6-difluorophenyl)methoxymethyl]-5-methyl-3-(3-methylthiophen-2-yl)-4h-1,2-oxazole Chemical compound C1=CSC(C=2CC(C)(COCC=3C(=CC=CC=3F)F)ON=2)=C1C OPEJGICLTMWFNQ-UHFFFAOYSA-N 0.000 abstract 1
- GZJVZGUUTYWVTP-UHFFFAOYSA-N 6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-1h-pyridazin-4-one Chemical compound N=1N=C(Cl)C=C(O)C=1OC=1C(C)=CC=CC=1C1CC1 GZJVZGUUTYWVTP-UHFFFAOYSA-N 0.000 abstract 1
- WBFYVDCHGVNRBH-UHFFFAOYSA-N 7,8-dihydropteroic acid Chemical compound N=1C=2C(=O)NC(N)=NC=2NCC=1CNC1=CC=C(C(O)=O)C=C1 WBFYVDCHGVNRBH-UHFFFAOYSA-N 0.000 abstract 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 1
- 108010000700 Acetolactate synthase Proteins 0.000 abstract 1
- 229930192334 Auxin Natural products 0.000 abstract 1
- VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 abstract 1
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005644 Dazomet Substances 0.000 abstract 1
- 229940122799 Dihydropteroate synthase inhibitor Drugs 0.000 abstract 1
- PHVNLLCAQHGNKU-UHFFFAOYSA-N Dimethipin Chemical compound CC1=C(C)S(=O)(=O)CCS1(=O)=O PHVNLLCAQHGNKU-UHFFFAOYSA-N 0.000 abstract 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 abstract 1
- YQVMVCCFZCMYQB-UHFFFAOYSA-N Flamprop Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-UHFFFAOYSA-N 0.000 abstract 1
- GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 abstract 1
- PMAAYIYCDXGUAP-UHFFFAOYSA-N Indanofan Chemical compound O=C1C2=CC=CC=C2C(=O)C1(CC)CC1(C=2C=C(Cl)C=CC=2)CO1 PMAAYIYCDXGUAP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005983 Maleic hydrazide Substances 0.000 abstract 1
- BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 abstract 1
- OKIBNKKYNPBDRS-UHFFFAOYSA-N Mefluidide Chemical compound CC(=O)NC1=CC(NS(=O)(=O)C(F)(F)F)=C(C)C=C1C OKIBNKKYNPBDRS-UHFFFAOYSA-N 0.000 abstract 1
- 239000002169 Metam Substances 0.000 abstract 1
- FMINYZXVCTYSNY-UHFFFAOYSA-N Methyldymron Chemical compound C=1C=CC=CC=1N(C)C(=O)NC(C)(C)C1=CC=CC=C1 FMINYZXVCTYSNY-UHFFFAOYSA-N 0.000 abstract 1
- 239000005642 Oleic acid Substances 0.000 abstract 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 1
- FCOHEOSCARXMMS-UHFFFAOYSA-N Oxaziclomefone Chemical compound C1OC(C)=C(C=2C=CC=CC=2)C(=O)N1C(C)(C)C1=CC(Cl)=CC(Cl)=C1 FCOHEOSCARXMMS-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 239000005643 Pelargonic acid Substances 0.000 abstract 1
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 abstract 1
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 abstract 1
- 239000002363 auxin Substances 0.000 abstract 1
- 239000007844 bleaching agent Substances 0.000 abstract 1
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 abstract 1
- 150000001733 carboxylic acid esters Chemical class 0.000 abstract 1
- 230000008166 cellulose biosynthesis Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 abstract 1
- SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 abstract 1
- 102000005396 glutamine synthetase Human genes 0.000 abstract 1
- 108020002326 glutamine synthetase Proteins 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 abstract 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- RBNIGDFIUWJJEV-LLVKDONJSA-N methyl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-LLVKDONJSA-N 0.000 abstract 1
- RBNIGDFIUWJJEV-UHFFFAOYSA-N methyl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-UHFFFAOYSA-N 0.000 abstract 1
- LINPVWIEWJTEEJ-UHFFFAOYSA-N methyl 2-chloro-9-hydroxyfluorene-9-carboxylate Chemical group C1=C(Cl)C=C2C(C(=O)OC)(O)C3=CC=CC=C3C2=C1 LINPVWIEWJTEEJ-UHFFFAOYSA-N 0.000 abstract 1
- PBTHJVDBCFJQGG-UHFFFAOYSA-N methyl azide Chemical compound CN=[N+]=[N-] PBTHJVDBCFJQGG-UHFFFAOYSA-N 0.000 abstract 1
- 229940102396 methyl bromide Drugs 0.000 abstract 1
- 230000011278 mitosis Effects 0.000 abstract 1
- JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 230000029553 photosynthesis Effects 0.000 abstract 1
- 238000010672 photosynthesis Methods 0.000 abstract 1
- IKVXBIIHQGXQRQ-CYBMUJFWSA-N propan-2-yl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-CYBMUJFWSA-N 0.000 abstract 1
- IKVXBIIHQGXQRQ-UHFFFAOYSA-N propan-2-yl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-UHFFFAOYSA-N 0.000 abstract 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 150000007970 thio esters Chemical class 0.000 abstract 1
- 150000004669 very long chain fatty acids Chemical class 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Reivindicación 1: Composición herbicida que comprende como componente A) un compuesto de isoxazolo[5,4-b]piridina de la fórmula (1) en donde las variables son como se definen a continuación: R¹ es hidrógeno, halógeno, C₁₋₆-alquilo o C₁₋₆-haloalquilo; R² es hidrógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-hidroxialquilo, C₃₋₆-cicloalquilo, C₃₋₆-halocicloalquilo, C₂₋₆-alquenilo o C₂₋₆-alquinilo; R³ es hidrógeno, halógeno, hidroxi, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-hidroxialquilo, C₁₋₆-alcoxi-C₁₋₆-alquilo, C₁₋₆-haloalcoxi-C₁₋₆-alquilo, C₃₋₆-cicloalquil-C₁₋₆-alquilo, C₃₋₆-halocicloalquil-C₁₋₆-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-halocicloalquilo, C₁₋₄-alquil-C₃₋₆-cicloalquilo, C₃₋₆-cicloalquenilo, C₃₋₆-halocicloalquenilo, fenil-C₁₋₆-alquilo, heterociclil-C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₂₋₆-haloalquinilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, amino, C₁₋₆-alquilamino, N,N-di-C₁₋₆-alquilamino, heterociclilo o fenilo; en donde el heterociclilo es un anillo monocíclico saturado, parcialmente insaturado o aromático de 5 ó 6 miembros, que contiene 1, 2, 3 ó 4 heteroátomos del grupo que consiste en O, N y S como miembros del anillo; y en donde las porciones heterociclilo y fenilo de R³ pueden ser no sustituidas o sustituidas con uno o más radicales seleccionados de halógeno, hidroxi, nitro, ciano, C₁₋₄-alquilo, C₁₋₄-haloalquilo, C₁₋₄-alcoxi-C₁₋₄-alquilo, C₃₋₆-cicloalquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₄-alcoxi, C₁₋₄-haloalcoxi, C₁₋₄-alcoxicarbonilo, C₁₋₄-alquiltio, C₁₋₄-alquilsulfinilo, C₁₋₄-alquilsulfonilo, amino, C₁₋₄-alquilamino, N,N-di-C₁₋₄-alquilamino, heterociclilo y fenilo; o su sal, amida, tioéster o éster carboxílico aceptables en la agricultura; y como componente B) al menos un herbicida adicional seleccionado de las clases b1) a b15): b1) inhibidores de la biosíntesis de lípidos; b2) inhibidores de la acetolactato sintasa; b3) inhibidores de la fotosíntesis; b4) inhibidores de protoporfirinógeno-IX oxidasa; b5) herbicidas de lejía; b6) inhibidor de la enolpiruvil shiquimato 3-fosfato sintasa; b7) inhibidores de glutamina sintetasa; b8) inhibidor de la 7,8-dihidropteroato sintasa; b9) inhibidores de mitosis; b10) inhibidores de la síntesis de ácidos grasos de cadena muy larga; b11) inhibidores de la biosíntesis de celulosa; b12) herbicidas desacopladores; b13) herbicidas auxínicos; b14) inhibidores del transporte de auxina; y b15) otros herbicidas seleccionados del grupo que consiste en bromobutide, chlorflurenol, chlorflurenol-metilo, 2-metilbenciléter de (1RS,2SR,4SR)-1,4-epoxi-p-ment-2-ilo, cumyluron, dalapon, dazomet, difenzoquat, difenzoquat-metilsulfato, dimethipin, DSMA, dymron, endothal y sus sales, etobenzanid, flamprop, flamprop-isopropilo, flamprop-metilo, flamprop-M-isopropilo, flamprop-M-metilo, flurenol, flurenol-butilo, flurprimidol, fosamine, fosamine-amonio, indanofan, hidrazida maleica, mefluidide, metam, methiozolin, azida de metilo, bromuro de metilo, metil-dymron, yoduro de metilo, MSMA, ácido oleico, oxaziclomefone, ácido pelargónico, pyributicarb, quinoclamine, triaziflam, tridiphane y 6-cloro-3-(2-ciclopropil-6-metilfenoxi)-4-piridazinol; que incluye sus sales o derivados aceptables en la agricultura. Reivindicación 8: El uso de una composición definida en cualquiera de las reivindicaciones 1 a 7, para controlar la vegetación no deseada. Reivindicación 10: Un método para controlar la vegetación no deseada, que comprende permitir que una composición, de acuerdo con cualquiera de las reivindicaciones 1 a 7, actúe en plantas, sus semillas y/o su hábitat.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461977663P | 2014-04-10 | 2014-04-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR100048A1 true AR100048A1 (es) | 2016-09-07 |
Family
ID=52807820
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150101076A AR100048A1 (es) | 2014-04-10 | 2015-04-09 | Composiciones herbicidas que comprenden isoxasolo[5,4-b]piridinas |
Country Status (13)
| Country | Link |
|---|---|
| US (4) | US10226046B2 (es) |
| EP (1) | EP3128843B1 (es) |
| JP (1) | JP2017510608A (es) |
| CN (1) | CN106163283A (es) |
| AR (1) | AR100048A1 (es) |
| AU (1) | AU2015243351B2 (es) |
| BR (1) | BR112016023273B1 (es) |
| CA (1) | CA2941350C (es) |
| CR (1) | CR20160524A (es) |
| EA (1) | EA031500B1 (es) |
| IL (1) | IL247527A0 (es) |
| MX (1) | MX2016013327A (es) |
| WO (1) | WO2015155236A1 (es) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112016023853A2 (pt) | 2014-04-17 | 2017-08-15 | Basf Se | composto, composição, método para controlar a vegetação indesejável e uso de um composto |
| WO2016062814A1 (en) | 2014-10-24 | 2016-04-28 | Basf Se | Substituted pyridine compounds having herbicidal activity |
| WO2016116531A1 (en) | 2015-01-22 | 2016-07-28 | BASF Agro B.V. | Ternary herbicidal combination comprising saflufenacil |
| ES2856454T3 (es) | 2015-05-08 | 2021-09-27 | Basf Agro Bv | Procedimiento para la preparación de epóxido de terpinoleno. |
| WO2016180614A1 (en) | 2015-05-08 | 2016-11-17 | Basf Se | A process for the preparation of limonene-4-ol |
| JP6808657B2 (ja) | 2015-06-19 | 2021-01-06 | ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆ Ｓｅ | テトラメチルキシリレンジイソシアネート及び少なくとも３つのアミン基を有するポリアミンから調製されるシェルを有するペンディメタリンマイクロカプセル |
| CR20180046A (es) | 2015-06-19 | 2018-04-30 | Basf Se | Microcápsulas plaguicidas con un revestimiento hecho de diisocianato de tetrametilxilileno, diisocianato cicloalifático y diamina alifática |
| US20180184658A1 (en) | 2015-07-10 | 2018-07-05 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and saflufenacil |
| EA201890268A1 (ru) | 2015-07-10 | 2018-07-31 | Басф Агро Б.В. | Гербицидная композиция, которая содержит цинметилин и диметенамид |
| KR102549057B1 (ko) | 2015-07-10 | 2023-06-29 | 바스프 아그로 비.브이. | 신메틸린 및 아세토클로르 또는 프레틸라클로르를 포함하는 제초제 조성물 |
| US20180184659A1 (en) | 2015-07-10 | 2018-07-05 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors |
| MY189172A (en) | 2015-07-10 | 2022-01-31 | Basf Agro Bv | Herbicidal composition comprising cinmethylin and specific quinolinecarboxylic acids |
| AU2016292678B2 (en) | 2015-07-10 | 2020-12-24 | BASF Agro B.V. | Method for controlling herbicide resistant or tolerant weeds |
| US20180199568A1 (en) | 2015-07-10 | 2018-07-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pethoxamid |
| JP6875369B2 (ja) | 2015-07-10 | 2021-05-26 | ビーエーエスエフ アグロ ベー．ブイ． | シンメチリン及びピロキサスルホンを含む除草剤組成物 |
| US11219215B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase |
| US11219212B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and imazamox |
| BR112018009625A8 (pt) | 2015-11-12 | 2019-02-26 | Basf Se | composições herbicida e agroquimica, utilização de uma composição e método para o controle da vegetação |
| WO2017215928A1 (en) | 2016-06-15 | 2017-12-21 | BASF Agro B.V. | Process for the epoxidation of a tetrasubstituted alkene |
| BR112018076030A2 (pt) | 2016-06-15 | 2019-03-26 | BASF Agro B.V. | processo de epoxidação de alqueno tetrassubstituído e uso de agente oxidante |
| WO2018108612A1 (en) | 2016-12-14 | 2018-06-21 | Basf Se | Herbicidal compositions comprising isoxazolo[5,4-b]pyridines |
| BR112020015344A2 (pt) | 2018-01-30 | 2020-12-08 | Upl Ltd | Combinações herbicidas |
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| US5252538A (en) * | 1984-05-21 | 1993-10-12 | American Cyanamid Company | (2-imidazolin-2-yl) fused heteropyridine compounds, intermediates for the preparation of and use of said compounds as herbicidal agents |
| US5665673A (en) * | 1988-12-29 | 1997-09-09 | Anderson; Richard J. | Potentiating herbicidal compositions |
| JP5412429B2 (ja) | 2007-07-23 | 2014-02-12 | クレストーン・インコーポレーテッド | 抗細菌性アミド及びスルホンアミド置換複素環式尿素化合物 |
| US8642660B2 (en) | 2007-12-21 | 2014-02-04 | The University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| US20110251063A1 (en) | 2008-12-18 | 2011-10-13 | Dschun Song | Heterocyclic diketone derivatives with herbicidal action |
| BR112012011059B8 (pt) * | 2009-11-13 | 2021-05-04 | Basf Se | uracilas, processo para preparar uracilas de fórmula i, (tio)carbamatos, composições herbicidas, processo para preparar composições de ativos herbicidas e método para controlar vegetação indesejada |
| US20130065760A1 (en) | 2010-03-23 | 2013-03-14 | Basf Se | Substituted Pyridines Having Herbicidal Action |
| KR20130041959A (ko) * | 2010-07-22 | 2013-04-25 | 바스프 에스이 | 제초성 이속사졸로[5,4-ｂ]피리딘 |
| IN2014CN04204A (es) * | 2012-01-12 | 2015-07-17 | Basf Se |
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| EP3128843B1 (en) | 2019-06-12 |
| BR112016023273B1 (pt) | 2021-09-14 |
| CA2941350C (en) | 2022-11-01 |
| CN106163283A (zh) | 2016-11-23 |
| US10881109B2 (en) | 2021-01-05 |
| WO2015155236A1 (en) | 2015-10-15 |
| US20170112130A1 (en) | 2017-04-27 |
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