AR077665A2 - Composicon herbicida y metodo para el control selectivo de malezas y yuyos en cultivos de plantas utiles - Google Patents
Composicon herbicida y metodo para el control selectivo de malezas y yuyos en cultivos de plantas utilesInfo
- Publication number
- AR077665A2 AR077665A2 ARP100102585A ARP100102585A AR077665A2 AR 077665 A2 AR077665 A2 AR 077665A2 AR P100102585 A ARP100102585 A AR P100102585A AR P100102585 A ARP100102585 A AR P100102585A AR 077665 A2 AR077665 A2 AR 077665A2
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- alkoxy
- haloalkoxy
- cyano
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 5
- 239000000203 mixture Substances 0.000 title abstract 3
- 239000004009 herbicide Substances 0.000 title abstract 2
- 244000038559 crop plants Species 0.000 title 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 26
- 229910052736 halogen Inorganic materials 0.000 abstract 26
- 150000002367 halogens Chemical class 0.000 abstract 26
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 26
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 25
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 25
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 25
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 24
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 22
- -1 C1- alkylsulfinyl 4 Chemical group 0.000 abstract 11
- 125000000217 alkyl group Chemical group 0.000 abstract 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 7
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 6
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 6
- 125000005240 diheteroarylamino group Chemical group 0.000 abstract 6
- 125000005241 heteroarylamino group Chemical group 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 4
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 4
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000005452 alkenyloxyalkyl group Chemical group 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 3
- 125000001188 haloalkyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 3
- 125000005326 heteroaryloxy alkyl group Chemical group 0.000 abstract 3
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- 125000004971 nitroalkyl group Chemical group 0.000 abstract 3
- 125000005359 phenoxyalkyl group Chemical group 0.000 abstract 3
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 3
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 2
- 241000196324 Embryophyta Species 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000006843 cycloalkyl-C1-5-alkyl Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- MAYMYMXYWIVVOK-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2)C(O)=O)=N1 MAYMYMXYWIVVOK-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000005531 Flufenacet Substances 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005577 Mesosulfuron Substances 0.000 abstract 1
- 239000005578 Mesotrione Substances 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 1
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 125000003396 thiol group Chemical class [H]S* 0.000 abstract 1
- 244000045561 useful plants Species 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
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
Una composicion herbicida que comprende como ingrediente activo, además de los adyuvantes de formulacion inertes habituales, una mezcla de a) una cantidad herbicida efectiva de un compuesto de la formula (1) en la cual R1 y R3 son, cada uno independientemente entre sí, halogeno, nitro, ciano, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-6, cicloalquilo C3-6, cicloalquilo C3-6 halo-substituido, alcoxialquilo C2-6, alquiltioalquilo C2-6, hidroxilo, mercapto, alcoxilo C1-6, alqueniloxilo C3-6, alquiniloxilo C3-6, carbonilo, carboxilo, alquilcarbonilo C1-4, hidroxialquilo C1-4, alcoxicarbonilo C1-4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, amino, alquilamino C1-4 o di(alquil C1-4) amino; R4 y R5 conjuntamente son un grupo -C-R6(R7)-O-C-R8(R9)-C-R10(R11)-C-R12(R13)- (Z1), -C-R1 4(R15)-C-R16(R17)-O-C-R18(R19)-C-R20(R21)- (Z2) o -C-R22(R23)-C-R24(R25)-C-R26(R27)-O-C-R28(R29)- (Z3), en los cuales R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19, R20, R21, R22, R23, R24, R25, R26, R27, R28 y R29 son, cada uno independientemente entre sí, hidrogeno, halogeno, alquilo C1-4 o haloalquilo C1-4, donde es posible para un anillo de alquileno, que conjuntamente con los átomos de carbono de los grupos Z1, Z2 o Z3, contenga de 2 a 6 átomos de carbono y que pueda estar interrumpido por oxígeno, estar ya sea condensado o formando una union de tipo espiro con los átomos de carbono de los grupos Z1, Z2 o Z3, o que el anillo de alquileno se una por lo menos a un átomo del anillo de los grupos Z1, Z2 o Z3; G es hidrogeno, -C(X1)-R30, -C(X2)-X3-R31, -C(X4)-N(R32)-R33, -SO2-R34, un cation de metal alcalino, de metal alcalinotérreo, de sulfonio o de amonio, o -P(X5)(R35)-R36, o -CH2-X6-R37; X1, X2, X3, X4, X5 y X6 son, cada uno independientemente entre sí, oxígeno o azufre; R30, R31, R32 y R33 son, cada uno independientemente entre sí, hidrogeno, alquilo C1-10, haloalquilo C1-10, cianoalquilo C1-10, nitroalquilo C1-10, aminoalquilo C1-10, alquilamino C1-5-alquilo C1-5, dialquilamino C2-8-alquilo C1-5, cicloalquil C3-7-alquilo C1-5, alcoxialquilo C2-10, alqueniloxialquilo C4-10, alquiniloxialquilo C4-10, alquiltioalquilo C2-10, alquilsulfoxil C1-5-alquilo C1-5, alquilsulfonil C1-5-alquilo C1-5, alquilidenaminooxi C2-8-alquilo C1-5, alquilcarbonil C1-5-alquilo C1-5, alcoxicarbonil C1-5-alquilo C1-5, aminoalquil C1-5-carbonil alquilo C1-5, dialquilaminocarbonil C2-8-alquilo C1-5, alquilcarbonilamino C1-5-alquilo C1-5, alquilcarbonil C2-5-alquilamino C1-5-alquilo C1-5, trialquilsilil C3-6-alquilo C1-5, fenilalquilo C1-5, heteroarilalquilo C1-5, fenoxialquilo C1-5, heteroariloxialquilo C1-5, alquenilo C2-5, haloalquenilo C2-5, cicloalquilo C3-8, fenilo, o fenilo o heteroarilo substituidos con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; o heteroarilamino; heteroarilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; diheteroarilamino, diheteroarilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; fenilamino, fenilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; difenilamino, difenilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; cicloalquilamino C3-7, cicloalquilamino C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; dicicloalquilamino C3-7, dicicloalquilamino C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; cicloalcoxilo C3-7 o cicloalcoxilo C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; R34, R35 y R36 son, cada uno independientemente entre sí, hidrogeno, alquilo C1-10, haloalquilo C1-10, cianoalquilo C1-10, nitroalquilo C1-10, aminoalquilo C1-10, alquilamino C1-5-alquilo C1-5, dialquilamino C2-8-alquilo C1-5, cicloalquil C3-7-alquilo C1-5, alcoxialquilo C2-10, alqueniloxialquilo C4-10, alquiniloxialquilo C4-10, alquiltioalquilo C2-10, alquilsulfoxil C1-5-alquilo C1-5, alquilsulfonil C1-5-alquilo C1-5, alquilidenaminooxi C2-8-alquilo C1-5, alquilcarbonil C1-5-alquilo C1-5, alcoxicarbonil C1-5-alquilo C1-5, aminoalquil C1-5-carbonilalquilo C1-5, dialquilaminocarbonil C2-8-alquilo C1-5, alquilcarbonilamino C1-5-alquilo C1-5, alquilcarbonil C2-5-alquilamino C1-5-alquilo C1-5, trialquilsilil C3-6-alquilo C1-5, fenilalquilo C1-5, heteroarilalquilo C1-5, fenoxialquilo C1-5, heteroariloxialquilo C1-5, alquenilo C2-5, haloalquenilo C2-5, cicloalquilo C3-8, fenilo, o fenilo o heteroarilo substituidos con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; o heteroarilamino; heteroarilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; diheteroarilamino, diheteroarilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; fenilamino, fenilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; difenilamino, difenilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; cicloalquilamino C3-7, cicloalquilamino C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; dicicloalquilamino C3-7, dicicloalquilamino C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; cicloalcoxilo C3-7, cicloalcoxilo C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; alcoxilo C1-10, haloalcoxilo C1-10, alquilamino C1-5, dialquilamino C2-8 y benciloxilo o fenoxilo, donde es posible en el caso de los grupos bencilo y fenilo que los mismos estén a su vez substituidos con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano, formilo, acetilo, propionilo, carboxilo, alcoxicarbonilo C1-5, metiltio, etiltio o con nitro; y R37 es alquilo C1-10, haloalquilo C1-10, cianoalquilo C1-10, nitroalquilo C1-10, aminoalquilo C1-10, alquilamino C1-5-alquilo C1-5, dialquilamino C2-8-alquilo C1-5, cicloalquil C3-7-alquilo C1-5, alcoxialquilo C2-10, alqueniloxialquilo C4-10, alquiniloxialquilo C4-10, alquiltioalquilo C2-10, alquilsulfoxil C1-5-alquilo C1-5, alquilsulfonil C1-5-alquilo C1-5, alquilidenaminooxi C2-8-alquilo C1-5, alquilcarbonil C1-5-alquilo C1-5, alcoxicarbonil C1-5-alquilo C1-5, aminoalquil C1-5-carbonilalquilo C1-5, dialquilaminocarbonil C2-8-alquilo C1-5, alquilcarbonilamino C1-5-alquilo C1-5, alquilcarbonil C2-5-alquilamino C1-5-alquilo C1-5, trialquilsilil C3-6-alquilo C1-5, fenilalquilo C1-5, heteroarilalquilo C1-5, fenoxialquilo C1-5, heteroariloxialquilo C1-5, alquenilo C2-5, haloalquenilo C2-5, cicloalquilo C3-8, fenilo, o fenilo o heteroarilo substituidos con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; o heteroarilamino; heteroarilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; diheteroarilamino, diheteroarilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; fenilamino, fenilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; difenilamino, difenilamino substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; cicloalquilamino C3-7, cicloalquilamino C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; dicicloalquilamino C3-7, dicicloalquilamino C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; cicloalcoxilo C3-7, cicloalcoxilo C3-7 substituido con alquilo C1-3, haloalquilo C1-3, alcoxilo C1-3, haloalcoxilo C1-3, halogeno, ciano o nitro; o alquilcarbonilo o una sal o diasteromero de un compuesto de la formula (1), con la salvedad de que R1 y R3 no sean simultáneamente metilo; y (b) una cantidad efectiva a los efectos de la sinergia herbicida, de por lo menos un herbicida seleccionado entre mesosulfuron, mesotrione y flufenacet y método para el control selectivo de malezas y yuyos en cultivos de plantas utiles.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH17812001 | 2001-09-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR077665A2 true AR077665A2 (es) | 2011-09-14 |
Family
ID=4566254
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020103606A AR036581A1 (es) | 2001-09-27 | 2002-09-25 | Composicion herbicida |
| ARP100102585A AR077665A2 (es) | 2001-09-27 | 2010-07-15 | Composicon herbicida y metodo para el control selectivo de malezas y yuyos en cultivos de plantas utiles |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020103606A AR036581A1 (es) | 2001-09-27 | 2002-09-25 | Composicion herbicida |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7241720B2 (es) |
| EP (2) | EP1429610B1 (es) |
| CN (1) | CN1558720A (es) |
| AR (2) | AR036581A1 (es) |
| AT (2) | ATE369745T1 (es) |
| CA (1) | CA2457761A1 (es) |
| DE (2) | DE60221921T2 (es) |
| EA (2) | EA007011B1 (es) |
| ES (2) | ES2290836T3 (es) |
| PL (2) | PL207276B1 (es) |
| PT (2) | PT1429610E (es) |
| WO (1) | WO2003028466A2 (es) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10311300A1 (de) | 2003-03-14 | 2004-09-23 | Bayer Cropscience Ag | 2,4,6-Phenylsubstituierte cyclische Ketoenole |
| DE10331675A1 (de) | 2003-07-14 | 2005-02-10 | Bayer Cropscience Ag | Hetarylsubstituierte Pyrazolidindion-Derivate |
| DE102004014620A1 (de) * | 2004-03-25 | 2005-10-06 | Bayer Cropscience Ag | 2,4,6-phenylsubstituierte cyclische Ketoenole |
| DE102004035133A1 (de) * | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von substituierten, cyclischen Ketoenolen und Safenern |
| DE102004044827A1 (de) | 2004-09-16 | 2006-03-23 | Bayer Cropscience Ag | Jod-phenylsubstituierte cyclische Ketoenole |
| DE102005031787A1 (de) * | 2005-07-07 | 2007-01-18 | Bayer Cropscience Gmbh | Kulturpflanzenverträgliche herbizide Mittel enthaltend Herbizide Safener |
| DE102005059469A1 (de) | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
| DE102006007882A1 (de) | 2006-02-21 | 2007-08-30 | Bayer Cropscience Ag | Cycloalkyl-phenylsubstituierte cyclische Ketoenole |
| GB0621440D0 (en) | 2006-10-27 | 2006-12-06 | Syngenta Crop Protection Ag | Herbicidal compositions |
| WO2010102758A2 (de) | 2009-03-11 | 2010-09-16 | Bayer Cropscience Ag | Halogenalkylmethylenoxy-phenyl-substituierte ketoenole |
| DE102010008644A1 (de) | 2010-02-15 | 2011-08-18 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Zyklische Ketoenole zur Therapie |
| DK2806741T3 (da) | 2012-01-26 | 2020-05-18 | Bayer Ip Gmbh | Phenylsubstituerede ketoenoler til bekæmpelse af fiskeparasitter |
| CN105519547A (zh) * | 2015-12-23 | 2016-04-27 | 汤云鹤 | 一种含氟噻草胺和唑啉草酯的农药组合物及其在防治小麦田杂草中的应用 |
| WO2021205448A1 (en) | 2020-04-06 | 2021-10-14 | Adama Agan Ltd. | Co-crystals of antioxidants and active ingredients and use of antioxidants as stabilizer |
| CN114106016B (zh) * | 2020-08-29 | 2025-08-12 | 海利尔药业集团股份有限公司 | 一种苯基吡唑啉衍生物或其盐、组合物及其用途 |
| GB202117598D0 (en) * | 2021-12-06 | 2022-01-19 | Syngenta Crop Protection Ag | Herbicidal compositions |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19650955A1 (de) * | 1996-12-07 | 1998-06-10 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit N- [(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl] -5-methylsulfonamidomethyl-2-alkoxycarbonylbenzolsulfonamiden |
| US6001774A (en) * | 1997-05-06 | 1999-12-14 | Sumitomo Chemical Company, Limited | Herbicidal composition |
| DE19832017A1 (de) * | 1998-07-16 | 2000-01-27 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit substituierten Phenylsulfonylharnstoffen zur Unkrautbekämpfung in Reis |
| JP4154760B2 (ja) * | 1998-08-05 | 2008-09-24 | 住友化学株式会社 | 除草剤組成物 |
| AU762586B2 (en) * | 1999-09-07 | 2003-06-26 | Syngenta Participations Ag | Herbicidal composition |
| WO2001017351A1 (en) | 1999-09-07 | 2001-03-15 | Syngenta Participations Ag | Herbicidal composition |
| PT1481970E (pt) * | 1999-09-07 | 2006-07-31 | Syngenta Participations Ag | Novos herbicidas |
| DE50005448D1 (de) * | 1999-09-07 | 2004-04-01 | Syngenta Participations Ag | Herbizides mittel |
| EA200400989A1 (ru) | 2002-02-13 | 2005-02-24 | Зингента Партисипейшнс Аг | Гербицидная композиция |
-
2002
- 2002-08-26 PL PL388796A patent/PL207276B1/pl unknown
- 2002-09-25 AR ARP020103606A patent/AR036581A1/es active IP Right Grant
- 2002-09-26 EP EP02777229A patent/EP1429610B1/en not_active Expired - Lifetime
- 2002-09-26 EP EP05019511A patent/EP1602277B1/en not_active Expired - Lifetime
- 2002-09-26 CA CA002457761A patent/CA2457761A1/en not_active Abandoned
- 2002-09-26 DE DE60221921T patent/DE60221921T2/de not_active Expired - Lifetime
- 2002-09-26 AT AT05019511T patent/ATE369745T1/de not_active IP Right Cessation
- 2002-09-26 DE DE60211725T patent/DE60211725T2/de not_active Expired - Lifetime
- 2002-09-26 EA EA200400411A patent/EA007011B1/ru not_active IP Right Cessation
- 2002-09-26 PT PT02777229T patent/PT1429610E/pt unknown
- 2002-09-26 US US10/490,970 patent/US7241720B2/en not_active Expired - Lifetime
- 2002-09-26 PT PT05019511T patent/PT1602277E/pt unknown
- 2002-09-26 ES ES05019511T patent/ES2290836T3/es not_active Expired - Lifetime
- 2002-09-26 CN CNA028189701A patent/CN1558720A/zh active Pending
- 2002-09-26 AT AT02777229T patent/ATE326843T1/de not_active IP Right Cessation
- 2002-09-26 EA EA200501293A patent/EA010053B1/ru unknown
- 2002-09-26 PL PL368002A patent/PL205774B1/pl unknown
- 2002-09-26 WO PCT/EP2002/010829 patent/WO2003028466A2/en not_active Ceased
- 2002-09-26 ES ES02777229T patent/ES2261745T3/es not_active Expired - Lifetime
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Also Published As
| Publication number | Publication date |
|---|---|
| AR036581A1 (es) | 2004-09-15 |
| PT1429610E (pt) | 2006-10-31 |
| ES2261745T3 (es) | 2006-11-16 |
| DE60221921D1 (de) | 2007-09-27 |
| CN1558720A (zh) | 2004-12-29 |
| EP1429610B1 (en) | 2006-05-24 |
| EP1602277A3 (en) | 2005-12-28 |
| EA007011B1 (ru) | 2006-06-30 |
| EA010053B1 (ru) | 2008-06-30 |
| WO2003028466A3 (en) | 2003-10-30 |
| PT1602277E (pt) | 2007-11-14 |
| DE60221921T2 (de) | 2008-05-15 |
| CA2457761A1 (en) | 2003-04-10 |
| US20040266624A1 (en) | 2004-12-30 |
| DE60211725D1 (de) | 2006-06-29 |
| ATE369745T1 (de) | 2007-09-15 |
| EP1602277B1 (en) | 2007-08-15 |
| EP1429610A2 (en) | 2004-06-23 |
| PL205774B1 (pl) | 2010-05-31 |
| DE60211725T2 (de) | 2006-09-21 |
| EA200400411A1 (ru) | 2004-12-30 |
| WO2003028466A2 (en) | 2003-04-10 |
| US7241720B2 (en) | 2007-07-10 |
| PL368002A1 (en) | 2005-03-21 |
| ES2290836T3 (es) | 2008-02-16 |
| EA200501293A1 (ru) | 2006-02-24 |
| PL207276B1 (pl) | 2010-11-30 |
| ATE326843T1 (de) | 2006-06-15 |
| EP1602277A2 (en) | 2005-12-07 |
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