AR036385A1 - Composiciones herbicidas a base de arilcetonas substituidas, uso de estas para controlar plantas indeseables, metodo para controlar malezas, y proceso para preparar una composicion herbicida - Google Patents
Composiciones herbicidas a base de arilcetonas substituidas, uso de estas para controlar plantas indeseables, metodo para controlar malezas, y proceso para preparar una composicion herbicidaInfo
- Publication number
- AR036385A1 AR036385A1 ARP020102870A ARP020102870A AR036385A1 AR 036385 A1 AR036385 A1 AR 036385A1 AR P020102870 A ARP020102870 A AR P020102870A AR P020102870 A ARP020102870 A AR P020102870A AR 036385 A1 AR036385 A1 AR 036385A1
- Authority
- AR
- Argentina
- Prior art keywords
- halogen
- optionally
- alkyl
- cyano
- substituted
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 3
- 239000004009 herbicide Substances 0.000 title abstract 3
- 239000000203 mixture Substances 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 abstract 34
- 150000002367 halogens Chemical class 0.000 abstract 29
- -1 substituted aryl ketone Chemical class 0.000 abstract 23
- 125000004432 carbon atom Chemical group C* 0.000 abstract 21
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 21
- 125000000217 alkyl group Chemical group 0.000 abstract 16
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 14
- 125000004414 alkyl thio group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 7
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 4
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 abstract 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 2
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 abstract 2
- CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 abstract 2
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 abstract 2
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 abstract 2
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 abstract 2
- QGQSRQPXXMTJCM-UHFFFAOYSA-N Benfuresate Chemical compound CCS(=O)(=O)OC1=CC=C2OCC(C)(C)C2=C1 QGQSRQPXXMTJCM-UHFFFAOYSA-N 0.000 abstract 2
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 abstract 2
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 abstract 2
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 abstract 2
- FFQPZWRNXKPNPX-UHFFFAOYSA-N N-benzyl-2-[4-fluoro-3-(trifluoromethyl)phenoxy]butanamide Chemical compound C=1C=CC=CC=1CNC(=O)C(CC)OC1=CC=C(F)C(C(F)(F)F)=C1 FFQPZWRNXKPNPX-UHFFFAOYSA-N 0.000 abstract 2
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 2
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 2
- ORFPWVRKFLOQHK-UHFFFAOYSA-N amicarbazone Chemical compound CC(C)C1=NN(C(=O)NC(C)(C)C)C(=O)N1N ORFPWVRKFLOQHK-UHFFFAOYSA-N 0.000 abstract 2
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 abstract 2
- XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 0.000 abstract 2
- MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 abstract 2
- HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 0.000 abstract 2
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical compound COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 abstract 2
- FUHMZYWBSHTEDZ-UHFFFAOYSA-M bispyribac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C([O-])=O)=N1 FUHMZYWBSHTEDZ-UHFFFAOYSA-M 0.000 abstract 2
- 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 2
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 abstract 2
- HFEJHAAIJZXXRE-UHFFFAOYSA-N cafenstrole Chemical compound CCN(CC)C(=O)N1C=NC(S(=O)(=O)C=2C(=CC(C)=CC=2C)C)=N1 HFEJHAAIJZXXRE-UHFFFAOYSA-N 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 abstract 2
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical compound C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- VIXCLRUCUMWJFF-KGLIPLIRSA-N (1R,5S)-benzobicyclon Chemical compound CS(=O)(=O)c1ccc(C(=O)C2=C(Sc3ccccc3)[C@H]3CC[C@H](C3)C2=O)c(Cl)c1 VIXCLRUCUMWJFF-KGLIPLIRSA-N 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- KNGWEAQJZJKFLI-UHFFFAOYSA-N 2,2-dimethyl-4h-1,3-benzodioxine-6-carbaldehyde Chemical compound O=CC1=CC=C2OC(C)(C)OCC2=C1 KNGWEAQJZJKFLI-UHFFFAOYSA-N 0.000 abstract 1
- XTFNPKDYCLFGPV-UHFFFAOYSA-N 2,6-dibromo-4-[(2,4-dinitrophenoxy)iminomethyl]phenol Chemical compound C1=C(Br)C(O)=C(Br)C=C1C=NOC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O XTFNPKDYCLFGPV-UHFFFAOYSA-N 0.000 abstract 1
- IOYNQIMAUDJVEI-UHFFFAOYSA-N 2-[N-(3-chloroprop-2-enoxy)-C-ethylcarbonimidoyl]-3-hydroxy-5-(oxan-4-yl)cyclohex-2-en-1-one Chemical compound C1C(=O)C(C(=NOCC=CCl)CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-UHFFFAOYSA-N 0.000 abstract 1
- IOYNQIMAUDJVEI-ZFNPBRLTSA-N 2-[N-[(E)-3-chloroprop-2-enoxy]-C-ethylcarbonimidoyl]-3-hydroxy-5-(oxan-4-yl)cyclohex-2-en-1-one Chemical compound C1C(=O)C(C(=NOC\C=C\Cl)CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-ZFNPBRLTSA-N 0.000 abstract 1
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 abstract 1
- VIXCLRUCUMWJFF-UHFFFAOYSA-N 3-[2-chloro-4-(methylsulfonyl)benzoyl]-4-(phenylthio)bicyclo[3.2.1]oct-3-en-2-one Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C(C(C1CCC2C1)=O)=C2SC1=CC=CC=C1 VIXCLRUCUMWJFF-UHFFFAOYSA-N 0.000 abstract 1
- UHIGORQILAXUPA-UHFFFAOYSA-N 3-propyl-1h-2,1,3-benzothiadiazin-4-one Chemical compound C1=CC=C2C(=O)N(CCC)SNC2=C1 UHIGORQILAXUPA-UHFFFAOYSA-N 0.000 abstract 1
- DXBQEHHOGRVYFF-UHFFFAOYSA-N 3-pyridin-4-ylpentane-2,4-dione Chemical group CC(=O)C(C(C)=O)C1=CC=NC=C1 DXBQEHHOGRVYFF-UHFFFAOYSA-N 0.000 abstract 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 abstract 1
- OXBQPMMCGPSGGD-UHFFFAOYSA-N 4-n-ethyl-6-methylsulfanyl-2-n-propyl-1,3,5-triazine-2,4-diamine Chemical compound CCCNC1=NC(NCC)=NC(SC)=N1 OXBQPMMCGPSGGD-UHFFFAOYSA-N 0.000 abstract 1
- OULHKCHGEGBIJF-UHFFFAOYSA-N 5-(3-butanoyl-2,4,6-trimethylphenyl)-2-(3-ethoxyiminopropyl)-3-hydroxycyclohex-2-en-1-one Chemical compound CCCC(=O)C1=C(C)C=C(C)C(C2CC(=O)C(CCC=NOCC)=C(O)C2)=C1C OULHKCHGEGBIJF-UHFFFAOYSA-N 0.000 abstract 1
- 239000002890 Aclonifen Substances 0.000 abstract 1
- 239000003666 Amidosulfuron Substances 0.000 abstract 1
- NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005469 Azimsulfuron Substances 0.000 abstract 1
- 239000005470 Beflubutamid Substances 0.000 abstract 1
- 239000005471 Benfluralin Substances 0.000 abstract 1
- 239000005472 Bensulfuron methyl Substances 0.000 abstract 1
- JDWQITFHZOBBFE-UHFFFAOYSA-N Benzofenap Chemical compound C=1C=C(Cl)C(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 JDWQITFHZOBBFE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005484 Bifenox Substances 0.000 abstract 1
- XTFNPKDYCLFGPV-OMCISZLKSA-N Bromofenoxim Chemical compound C1=C(Br)C(O)=C(Br)C=C1\C=N\OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O XTFNPKDYCLFGPV-OMCISZLKSA-N 0.000 abstract 1
- 239000005489 Bromoxynil Substances 0.000 abstract 1
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 abstract 1
- ZOGDSYNXUXQGHF-XIEYBQDHSA-N Butroxydim Chemical compound CCCC(=O)C1=C(C)C=C(C)C(C2CC(=O)C(\C(CC)=N\OCC)=C(O)C2)=C1C ZOGDSYNXUXQGHF-XIEYBQDHSA-N 0.000 abstract 1
- 239000005492 Carfentrazone-ethyl Substances 0.000 abstract 1
- DXXVCXKMSWHGTF-UHFFFAOYSA-N Chlomethoxyfen Chemical compound C1=C([N+]([O-])=O)C(OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 DXXVCXKMSWHGTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000005531 Flufenacet Substances 0.000 abstract 1
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 abstract 1
- SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 0.000 abstract 1
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000001316 cycloalkyl alkyl 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
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- LYPWWQLKWQNQKV-UHFFFAOYSA-N methyl 2-[5-ethyl-2-[[4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]phenoxy]methyl]phenoxy]propanoate Chemical compound COC(=O)C(C)OC1=CC(CC)=CC=C1COC1=CC=C(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)C=C1 LYPWWQLKWQNQKV-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229960002939 metizoline Drugs 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- HZDIJTXDRLNTIS-DAXSKMNVSA-N n-[[(z)-but-2-enoxy]methyl]-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(COC\C=C/C)C(=O)CCl HZDIJTXDRLNTIS-DAXSKMNVSA-N 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000002071 phenylalkoxy group Chemical group 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 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
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
-
- 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
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
- A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic 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
Composiciones herbicidas, que tienen una cantidad efectiva de una combinación de compuestos activos que comprende (a) al menos una arilcetona sustituida de la fórmula (1) en la que A significa alcanodiilo (alquileno) C1-6, R1 significa uno de los agrupamientos del conjunto de fórmulas (2) donde m significa los números 0 hasta 6; R5 significa halógeno, significa alquilo, alcoxicarbonilo ó alquiltio con respectivamente 1 hasta 6 átomos de carbono en los grupos alquilo sustituidos, respectiva y opcionalmente con ciano, con halógeno ó con alcoxi C1-4, ó significa fenilo sustituido opcionalmente con halógeno, con alquilo C1-4 ó con alcoxi C1-4, ó -en el caso en que m signifique 2- opcionalmente también junto con un segundo radical R5 significa un grupo carbonilo (C=O) ó alcanodiilo (alquileno) con 2 hasta 6 átomos de carbono; R6 significa hidroxilo, formiloxi, halógeno, significa alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, alquilcarboniloxi, alcoxicarboniloxi, alquilaminocarboniloxi ó alquilsulfoniloxi con, respectivamente 1 hasta 6 átomos de carbono en los grupos alquilo, sustituidos, respectiva y opcionalmente con ciano, con halógeno o con alcoxi C1-4, significa alqueniloxi o alquiniloxi con, respectivamente, 2 hasta 6 átomos de carbono, sustituidos, respectiva y opcionalmente con ciano o con halógeno, o significa fenoxi, feniltio, fenilsulfinilo, fenilsulfonilo, fenilcarboniloxi, fenilcarbonilalcoxi, fenilsulfoniloxi, fenilalcoxi, fenilalquiltio, fenilalquilsulfinilo ó fenilalquilsulfonilo con, opcionalmente, 1 hasta 4 átomos de carbono en la parte alquilo, sustituidos, respectiva y opcionalmente con nitro, con ciano, con halógeno, con alquilo C1-4, con halógenoalquilo C1-4, con alcoxi C1-4 ó con halógenoalcoxi C1-4; R7 significa hidrógeno, ciano, carbamoilo, tiocarbamoilo, halógeno, significa alquilo, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo ó alcoxicarbonilo con, respectivamente, 1 hasta 6 átomos de carbono en los grupos alquilo sustituidos, respectiva y opcionalmente con ciano, con halógeno o con alcoxi C1-4, o significa cicloalquilo con 3 hasta 6 átomos de carbono sustituido, opcionalmente con ciano, con halógeno ó con alquilo C1-4; R8 significa hidrógeno, significa alquilo con 1 hasta 6 átomos de carbono sustituido, opcionalmente con ciano, con halógeno o con alcoxi C1-4, significa alquenilo o alquinilo con, respectivamente, 2 hasta 6 átomos de carbono sustituidos, respectiva y opcionalmente con ciano o con halógeno, significa cicloalquilo ó cicloalquilalquilo con, respectivamente, 3 hasta 6 átomos de carbono en los grupos cicloalquilo y, opcionalmente 1 hasta 4 átomos de carbono en la parte alquilo sustituidos, respectiva y opcionalmente con ciano, con halógeno o con alquilo C1-4, o significa fenilo ó fenil-alquilo C1-4 sustituidos, respectiva y opcionalmente con nitro, con ciano, con halógeno, con alquilo C1-4, con halógenoalquilo C1-4, con alcoxi C1-4 o con halógenoalcoxi C1-4; R9 significa hidroxilo, formiloxi, significa alcoxi, alquilcarboniloxi, alcoxicarboniloxi, alquilaminocarboniloxi ó alquilsulfoniloxi con, respectivamente, 1 hasta 6 átomos de carbono en los grupos alquilo sustituidos, respectiva y opcionalmente con ciano, con halógeno o con alcoxi C1-4, significa alqueniloxi ó alquiniloxi con, respectivamente, 2 hasta 6 átomos de carbono sustituidos, respectiva y opcionalmente con ciano o con halógeno, significa fenilalcoxi, fenilcarboniloxi, fenilcarbonilalcoxi ó fenilsulfoniloxi con, opcionalmente, 1 hasta 4 átomos de carbono en la parte alquilo sustituidos, respectiva y opcionalmente con nitro, con ciano, con halógeno, con alquilo C1-4 o con halógenoalquilo C1-4; R10 significa hidrógeno, ciano, carbamoilo, tiocarbamoilo, halógeno, ó significa alquilo, alquilcarbonilo, alcoxi, alcoxicarbonilo, alquiltio alquilsulfinilo ó alquilsulfonilo con, respectivamente, 1 hasta 6 átomos de carbono en los grupos alquilo sustituidos, respectiva y opcionalmente con ciano, con halógeno o con alcoxi C1-4; R11 significa hidrógeno, significa alquilo con 1 hasta 6 átomos de carbono sustituido, opcionalmente con ciano, con halógeno o con alcoxi C1-4 ó significa cicloalquilo con 3 hasta 6 átomos de carbono sustituido, opcionalmente con ciano, con halógeno o con alquilo C1-4; R12 significa hidrógeno, significa alquilo C1-6 sustituido, opcionalmente con ciano, con halógeno o con alcoxi C1-4 o significa cicloalquilo con 3 hasta 8 átomos de carbono sustituido, opcionalmente con ciano, con halógeno o con alquilo C1-4; y R13 significa hidrógeno, ciano, carbamoilo, halógeno, ó significa alquilo, alcoxi, alcoxicarbonilo, alquiltio, alquilsulfinilo ó alquilsulfonilo con, respectivamente, 1 hasta 6 átomos de carbono en los grupos alquilo sustituidos, respectiva y opcionalmente con ciano, con halógeno o con alcoxi C1-4; R2 significa hidrógeno, nitro, ciano, carboxilo, carbamoilo, tiocarbamoilo, halógeno, ó significa alquilo, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, alquilamino, dialquilamino ó dialquilaminosulfonilo con, respectivamente, 1 hasta 6 átomos de carbono en los grupos alquilo, sustituidos, respectiva y opcionalmente con ciano con halógeno o con alcoxi C1-4, con alquiltio C1-4, con alquilsulfinilo C1-4 o con alquilsulfonilo C1-4; R3 significa hidrógeno, nitro, ciano, carboxilo, carbamoilo, tiocarbamoilo, halógeno, ó significa alquilo, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, alquilamino, dialquilamino ó dialquilaminosulfonilo con, respectivamente, 1 hasta 6 átomos de carbono en los grupos alquilo sustituidos, respectiva y opcionalmente con ciano, con halógeno o con alcoxi C1-4, con alquiltio C1-4, con alquilsulfinilo C1-4 o con alquilsulfonilo C1-4, y R4 significa un agrupamiento heterocíclico, sustituido opcionalmente con 4 hasta 12 miembros, saturado o insaturado, monocíclico o bicíclico, que contiene 1 hasta 4 heteroátomos, siendo hasta cuatro de los mismos átomos de nitrógeno y, opcionalmente -de manera alternativa o adicional- de 1 hasta 3 átomos de oxígeno, átomos de azufre, grupos -SO-, grupos -SO2-, grupos -CO- y/o grupos -CS-, -con inclusión de todas las posibles formas tautómeras de los compuestos de la fórmula general (1) y de las posibles sales o bien aductos con ácidos o con bases de los compuestos de la fórmula general (1) - ("Compuestos activos del grupo 1"); y (b) uno o varios compuestos de un segundo grupo de herbicidas, que contiene los compuestos activos citados a continuación: 4-(2-cloro-fenilo)-N-ciclohexil-N-etil-4,5-dihidro-5-oxo-1H-tetrazol-1-carboxamida (Fentrazamide), N-(4-fluoro-fenil)-N-i-propilo-2-(5-trifluorometil-1,3,4-tiadiazol-2-iloxi)-acetamida (Flufenacet), 2-cloro-N-(etoximetil)-N-(2-etil-6-metil-fenil)-acetamida (Acetochlor), ácido 5-(2-cloro-4-trifluorometil-fenoxi)-2-nitro-benzoico - sal sódica (Acifluorfen-sodio), 2-cloro-6-nitro-3-fenoxi-bencenamina (Aclonifen), 2-cloro-N-(metoximetil)-N-(2,6-dietil-fenil)-acetamida (Alachlor), N-etil-N'-i-propil-6-metiltio-1,3,5-triazin-2,4-diamina (Ametryn), 4-amino-N-(1,1-dimetil-etil)-4,5-dihidro-3-(1-metil-etil)-5-oxo-1H-1,2,4-triazol-1-carboxamida (Amicarbazone), N-(4,6-dimetoxi-pirimidin-2-il)-N'-(N-metil-N-metilsulfonil-sulfamoil)-urea (Amidosulfuron), 1H-1,2,4-triazol-3-amina (Amitrole), S-[2-[(4-cloro-fenil)-(1-isopropil)-amino]-2-oxo-etil]-O,O-dimetil-fosforoditioato (Anilofos), 6-cloro-4-etilamino-2-isopropilamino-1,3,5-triazina (Atrazin), 2-[2,4-dicloro-5-(2-propiniloxi)-fenilo]-5,6,7,8-tetrahidro-1,2,4-triazolo[4,3-a]piridin-3(2H)-ona (Azafenidin), N-(4,6-dimetoxi-pirimidin-2-il)-N'-[1-metil-4-(2-metil-2H-tetrazol-5-il)-1H-pirazol-5-ilsulfonil]-urea (Azimsulfuron), N-bencil-2-(4-fluoro-3-trifluorometil-fenoxi)-butanamida (Beflubutamid), ácido 4-cloro-2-oxo-3(2H)-benzotiazol-acético (Benazolin), N-butil-N-etil-2,6-dinitro-4-trifluorometil-bencenamina (Benfluralin), 2,3-dihidro-3,3-dimetil-5-benzofuranil-etansulfonato (Benfuresate), N-(4,6-dimetoxi-pirimidin-2-il)-N'-(2-metoxicarbonil-fenilmetilsulfonil)-urea (Bensulfuron-metilo), S-[(4-cloro-fenil)-metil]-dietiltiocarbamato (Benthiocarb, Thiobencarb), 2-[2-[4-(3,6-dihidro-3-metil-2,6-dioxo-4-trifluorometil-1(2H)-pirimidinilfenoximetil]-5-etil-fenoxi-propanoato de metilo (Benzfendizone), 3-(2-cloro-4-metilsulfonil-benzoil)-4-feniltio-biciclo[3.2.1]oct-3-en-2-ona (Benzobicyclon), 2-[[4-(2,4-dicloro-3-metil-benzoil)-1,3-dimetil-1H-pirazol-5-il]-oxi]-1-(4-metil-fenil)-etanona (Benzofenap), N-benzoil-N-(3,4-dicloro-fenil)-DL-alaninato de etilo (Benzoylprop-etilo), 3-i-propil-1H-2,1,3-benzotiadiazin-4(3H)-ona (Bentazon), 5-(2,4-dicloro-fenoxi)-2-nitro-benzoato de metilo (Bifenox), ácido 2,6-bis-(4,6-dimetoxi-pirimidin-2-iloxi)-benzoico - sal sódica (Bispyribac-sodio), 5-bromo-6-metil-3-(1-metilpropil)-2,4(1H,3H)pirimidindiona (Bromacil), 2-bromo-3,3-dimetil-N-(1-metil-1-fenil-etil)-butanamida (Bromobutide), 3,5-dibromo-4-hidroxibenzaldehído-O-(2,4-dinitro-fenil)-oxima (Bromofenoxim), 3,5-dibromo-4-hidroxi-benzonitrilo (Bromoxynil), N-butoximetil-2-cloro-N-(2,6-dietilfenil)-acetamida (Butachlor), 2-cloro-5-(3,6-dihidro-3-metil-2,6-dioxo-4-trifluorometil-1(2H)-pirimidinil)-benzoato de [1,1-dimetil-2-oxo-2-(2-propeniloxi)]-etilo (Butafenacil-alilo), tiofosforato de N-s-butilamido-O-etil-O-(5-metil-2-nitro-fenilo) (Butamifos), (Z)-2-cloro-N-[(2-buteniloxi)-metil]-N-(2,6-dietil-fenil)-acetamida (Butenachlor), 2-(1-etoximino-propil)-3-hidroxi-5-[2,4,6-trimetil-3-(1-oxo-butil)-fenil]-2-ciclohexen-1-ona (Butroxydim), S-etil-bis-(2-metil-propil)-tiocarbamato (Butylate), N,N-dietil-3-(2,4,6-trimetil-fenilsulfonil)-1H-1,2,4-triazol-1-carboxamida (Cafenstrole), 2-[1-[(3-cloro-2-propenil)-oxi-imino]-propil]-3-hidroxi-5-(tetrahidro-2H-piran-4-il)-2-ciclohexen-1-ona (Caloxydim, Tepraloxydim), 2-(4-cloro-2-fluoro-5-(2-cloro-2-etoxicarbonil-etil)-fenil)-4-difluorometil-5-metil-2,4-dihidro-3H-1,2,4-triazol-3-ona (Carfentrazone-etilo), 2,4-dicloro-1-(3-metoxi-4-nitrofenoxi)-benceno (Chlometoxyfen), ácido 3-amino-2,5-dicloro-benzoico (Chloramben), N-(4-cloro-6-m
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10142333A DE10142333A1 (de) | 2001-08-30 | 2001-08-30 | Herbizide Mischungen auf Basis von substituierten Arylketonen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR036385A1 true AR036385A1 (es) | 2004-09-08 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020102870A AR036385A1 (es) | 2001-08-30 | 2002-07-30 | Composiciones herbicidas a base de arilcetonas substituidas, uso de estas para controlar plantas indeseables, metodo para controlar malezas, y proceso para preparar una composicion herbicida |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20050192182A1 (es) |
| EP (1) | EP1423005A1 (es) |
| AR (1) | AR036385A1 (es) |
| CA (1) | CA2458766A1 (es) |
| DE (1) | DE10142333A1 (es) |
| WO (1) | WO2003020033A1 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10143083A1 (de) * | 2001-09-03 | 2003-03-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten Arylsulfonylaminocarbonyltriazolinonen und Safenern |
| CA2637027A1 (en) * | 2006-01-10 | 2007-07-19 | Ruey J. Yu | N-(phosphonoalkyl)-amino acids, derivatives thereof and compositions and methods of use |
| JP5213320B2 (ja) * | 2006-09-13 | 2013-06-19 | バイエル・クロップサイエンス・アーゲー | 薬害軽減された除草剤組成物 |
| WO2009089165A2 (en) * | 2008-01-07 | 2009-07-16 | Auburn University | Combinations of herbicides and safeners |
| EP2252146A2 (en) * | 2008-02-05 | 2010-11-24 | Arysta LifeScience North America, LLC | Solid formulation of low melting active compound |
| WO2009102689A2 (en) * | 2008-02-12 | 2009-08-20 | Arysta Lifescience North America, Llc | Method of controlling unwanted vegetation |
| DK2337452T3 (en) | 2008-07-03 | 2014-12-15 | Monsanto Technology Llc | COMBINATION OF derivatized SACCHARIDSURFAKTANTER AND ETHERAMINOXIDSURFAKTANTER AS HERBICIDADJUVANTER |
| TWI574622B (zh) * | 2012-05-22 | 2017-03-21 | Ishihara Sangyo Kaisha | Herbicidal composition |
| US9078443B1 (en) | 2014-01-31 | 2015-07-14 | Fmc Corporation | Methods for controlling weeds using formulations containing fluthiacet-methyl and HPPD herbicides |
| WO2025173004A1 (en) * | 2024-02-13 | 2025-08-21 | Adama Agan Ltd. | Herbicidal mixture comprising bifenox and chloroacetamide compound |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3525205A1 (de) * | 1984-09-11 | 1986-03-20 | Hoechst Ag, 6230 Frankfurt | Pflanzenschuetzende mittel auf basis von 1,2,4-triazolderivaten sowie neue derivate des 1,2,4-triazols |
| DE3939503A1 (de) * | 1989-11-30 | 1991-06-06 | Hoechst Ag | Neue pyrazoline zum schutz von kulturpflanzen gegenueber herbiziden |
| US5700758A (en) * | 1989-11-30 | 1997-12-23 | Hoechst Aktiengesellschaft | Pyrazolines for protecting crop plants against herbicides |
| US5529976A (en) * | 1990-01-10 | 1996-06-25 | Hoechst Aktiengesellschaft | Pyridyl sulphonyl ureas as herbicides and plant growth regulators |
| CA2073446C (en) * | 1990-01-10 | 2001-11-27 | Heinz Kehne | Pyridylsulfonylureas as herbicides and plant growth regulators, processes for their preparation and their use |
| WO1995030661A1 (de) * | 1994-05-04 | 1995-11-16 | Bayer Aktiengesellschaft | Substituierte aromatische thiocarbonsäureamide und ihre verwendung als herbizide |
| GB9424853D0 (en) * | 1994-12-09 | 1995-02-08 | Bayer Ag | New herbicidal compositions |
| US5846907A (en) * | 1995-02-24 | 1998-12-08 | Basf Aktiengesellschaft | Herbicidally active pyrazol-4-ylbenzoyl compounds |
| JP3687933B2 (ja) * | 1995-08-08 | 2005-08-24 | 株式会社エス・ディー・エス バイオテック | 水田用除草剤組成物 |
| WO1997009326A1 (en) * | 1995-09-07 | 1997-03-13 | Otsuka Kagaku Kabushiki Kaisha | Triazole derivatives, herbicide composition containing the same, and method for using the same |
| DE19621522A1 (de) * | 1996-05-29 | 1997-12-04 | Hoechst Schering Agrevo Gmbh | Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung |
| JP2001508075A (ja) * | 1997-01-17 | 2001-06-19 | ビーエーエスエフ アクチェンゲゼルシャフト | 硫黄含有2−クロロ−3−(4,5−ジヒドロ−3−イソキサゾリル)−安息香酸の製造法 |
| EA006633B1 (ru) * | 1997-01-17 | 2006-02-24 | Басф Акциенгезельшафт | Замещенные 3-гетероциклилом производные бензоила |
| US6165944A (en) * | 1997-01-17 | 2000-12-26 | Basf Aktiengesellschaft | 4-(3-heterocyclyl-1-benzoyl) pyrazoles and their use as herbicides |
| WO1998034480A1 (de) * | 1997-02-07 | 1998-08-13 | Novartis Ag | Herbizides mittel |
| WO1998038176A1 (en) * | 1997-02-26 | 1998-09-03 | Hokko Chemical Industry Co., Ltd. | 1-substituted 4-carbamoyl-1,2,4-triazol-5-one derivatives and herbicide |
| EP1001939B1 (de) * | 1997-08-07 | 2009-01-07 | Basf Se | Heterocyclisch substituierte 4-benzoyl-pyrazole als herbizide |
| DE19742951A1 (de) * | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung |
| EE04413B1 (et) * | 1998-06-16 | 2005-02-15 | Basf Aktiengesellschaft | Sünergilise toimega herbitsiidne segu |
| DE19827855A1 (de) * | 1998-06-23 | 1999-12-30 | Hoechst Schering Agrevo Gmbh | Kombinationen aus Herbiziden und Safenern |
| FR2785148B1 (fr) * | 1998-11-02 | 2000-12-15 | Rhone Poulenc Agrochimie | Nouvelles compositions herbicide a base de glyphosate et d'isoxazoles |
| DE19853827A1 (de) * | 1998-11-21 | 2000-05-25 | Aventis Cropscience Gmbh | Kombinationen aus Herbiziden und Safenern |
| DE19950943A1 (de) * | 1999-10-22 | 2001-05-17 | Aventis Cropscience Gmbh | Synergistische herbizide Mittel enthaltend Herbizide aus der Gruppe der Hemmstoffe der Hydroxyphenylpyruvat-Dioxygenase |
| DE19953136A1 (de) * | 1999-11-04 | 2001-05-10 | Aventis Cropscience Gmbh | Benzoylcyclohexandione und Benzoylpyrazole, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| JP2004504266A (ja) * | 2000-01-17 | 2004-02-12 | バイエル アクチェンゲゼルシャフト | 置換アリールケトン類 |
-
2001
- 2001-08-30 DE DE10142333A patent/DE10142333A1/de not_active Withdrawn
-
2002
- 2002-07-30 AR ARP020102870A patent/AR036385A1/es not_active Application Discontinuation
- 2002-08-19 WO PCT/EP2002/009243 patent/WO2003020033A1/de not_active Ceased
- 2002-08-19 CA CA002458766A patent/CA2458766A1/en not_active Abandoned
- 2002-08-19 EP EP02758472A patent/EP1423005A1/de not_active Withdrawn
- 2002-08-19 US US10/487,671 patent/US20050192182A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20050192182A1 (en) | 2005-09-01 |
| EP1423005A1 (de) | 2004-06-02 |
| WO2003020033A1 (de) | 2003-03-13 |
| CA2458766A1 (en) | 2003-03-13 |
| DE10142333A1 (de) | 2003-03-20 |
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