AR037324A1 - Herbicidas a base de tien-3-il-sulfonilamino(tio)carbonil-triazolin(tio)onas substituidas - Google Patents
Herbicidas a base de tien-3-il-sulfonilamino(tio)carbonil-triazolin(tio)onas substituidasInfo
- Publication number
- AR037324A1 AR037324A1 ARP020103559A ARP020103559A AR037324A1 AR 037324 A1 AR037324 A1 AR 037324A1 AR P020103559 A ARP020103559 A AR P020103559A AR P020103559 A ARP020103559 A AR P020103559A AR 037324 A1 AR037324 A1 AR 037324A1
- Authority
- AR
- Argentina
- Prior art keywords
- carbon atoms
- appropriate
- alkyl
- methyl
- cyano
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 28
- 125000000217 alkyl group Chemical group 0.000 abstract 18
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 17
- -1 mercapto, amino Chemical group 0.000 abstract 13
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 11
- 239000000460 chlorine Substances 0.000 abstract 11
- 229910052801 chlorine Inorganic materials 0.000 abstract 11
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 10
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 10
- 229910052794 bromium Inorganic materials 0.000 abstract 10
- 229910052731 fluorine Inorganic materials 0.000 abstract 10
- 239000011737 fluorine Substances 0.000 abstract 10
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical class 0.000 abstract 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 6
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 150000001875 compounds Chemical class 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
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 3
- 125000003282 alkyl amino group Chemical group 0.000 abstract 3
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 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
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-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
- 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 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-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
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio 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
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-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
- HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 0.000 abstract 2
- 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 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
- 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
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 abstract 2
- NSWAMPCUPHPTTC-UHFFFAOYSA-N chlorimuron-ethyl Chemical compound CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(Cl)=CC(OC)=N1 NSWAMPCUPHPTTC-UHFFFAOYSA-N 0.000 abstract 2
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- RNXRCBYXQZEUDV-UHFFFAOYSA-N 2,2-dioxo-3-propyl-1h-2$l^{6},1,3-benzothiadiazin-4-one Chemical compound C1=CC=C2NS(=O)(=O)N(CCC)C(=O)C2=C1 RNXRCBYXQZEUDV-UHFFFAOYSA-N 0.000 abstract 1
- GKECDORWWXXNRY-UHFFFAOYSA-N 2h-pyridin-3-one Chemical compound O=C1CN=CC=C1 GKECDORWWXXNRY-UHFFFAOYSA-N 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
- KKCLIBMLUMCTMZ-UHFFFAOYSA-N 3-methoxy-4-methyl-5-oxo-n-[2-(trifluoromethoxy)phenyl]sulfonyl-1,2,4-triazole-1-carboxamide;sodium Chemical compound [Na].O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1OC(F)(F)F KKCLIBMLUMCTMZ-UHFFFAOYSA-N 0.000 abstract 1
- ZOGDSYNXUXQGHF-UHFFFAOYSA-N 5-(3-butanoyl-2,4,6-trimethylphenyl)-2-(N-ethoxy-C-ethylcarbonimidoyl)-3-hydroxycyclohex-2-en-1-one Chemical compound CCCC(=O)C1=C(C)C=C(C)C(C2CC(=O)C(C(CC)=NOCC)=C(O)C2)=C1C ZOGDSYNXUXQGHF-UHFFFAOYSA-N 0.000 abstract 1
- 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 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
- QGQSRQPXXMTJCM-UHFFFAOYSA-N Benfuresate Chemical compound CCS(=O)(=O)OC1=CC=C2OCC(C)(C)C2=C1 QGQSRQPXXMTJCM-UHFFFAOYSA-N 0.000 abstract 1
- 239000005472 Bensulfuron methyl Substances 0.000 abstract 1
- 239000005476 Bentazone 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
- 239000005489 Bromoxynil Substances 0.000 abstract 1
- SPNQRCTZKIBOAX-UHFFFAOYSA-N Butralin Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O SPNQRCTZKIBOAX-UHFFFAOYSA-N 0.000 abstract 1
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005490 Carbetamide Substances 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-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
- 239000005493 Chloridazon (aka pyrazone) Substances 0.000 abstract 1
- 239000005494 Chlorotoluron 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
- 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 1
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 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
- 125000006323 alkenyl amino group Chemical group 0.000 abstract 1
- 125000005108 alkenylthio group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000005109 alkynylthio 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
- 125000004659 aryl alkyl thio group Chemical group 0.000 abstract 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract 1
- 125000001769 aryl amino group Chemical group 0.000 abstract 1
- 125000005110 aryl thio group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 0.000 abstract 1
- 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 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
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 abstract 1
- RYVIXQCRCQLFCM-UHFFFAOYSA-N bispyribac Chemical compound COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(O)=O)=N1 RYVIXQCRCQLFCM-UHFFFAOYSA-N 0.000 abstract 1
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 abstract 1
- JEDYYFXHPAIBGR-UHFFFAOYSA-N butafenacil Chemical compound O=C1N(C)C(C(F)(F)F)=CC(=O)N1C1=CC=C(Cl)C(C(=O)OC(C)(C)C(=O)OCC=C)=C1 JEDYYFXHPAIBGR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 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 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- XQNAUQUKWRBODG-UHFFFAOYSA-N chlornitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=C(Cl)C=C(Cl)C=C1Cl XQNAUQUKWRBODG-UHFFFAOYSA-N 0.000 abstract 1
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 abstract 1
- NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 abstract 1
- CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 abstract 1
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 1
- UAGGVDVXSRGPRP-UHFFFAOYSA-N diethylcarbamothioic s-acid Chemical compound CCN(CC)C(S)=O UAGGVDVXSRGPRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- QMTNOLKHSWIQBE-FGTMMUONSA-N exo-(+)-cinmethylin Chemical compound O([C@H]1[C@]2(C)CC[C@@](O2)(C1)C(C)C)CC1=CC=CC=C1C QMTNOLKHSWIQBE-FGTMMUONSA-N 0.000 abstract 1
- JFUIHGAGFMFNRD-UHFFFAOYSA-N fica Chemical compound FC1=CC=C2NC(C(=O)NCCS)=CC2=C1 JFUIHGAGFMFNRD-UHFFFAOYSA-N 0.000 abstract 1
- UOUXAYAIONPXDH-UHFFFAOYSA-M flucarbazone-sodium Chemical compound [Na+].O=C1N(C)C(OC)=NN1C(=O)[N-]S(=O)(=O)C1=CC=CC=C1OC(F)(F)F UOUXAYAIONPXDH-UHFFFAOYSA-M 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-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
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 1
- 230000008635 plant growth Effects 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- RVULBHWZFCBODE-UHFFFAOYSA-M sodium;5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical compound [Na+].C1=C([N+]([O-])=O)C(C(=O)[O-])=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 RVULBHWZFCBODE-UHFFFAOYSA-M 0.000 abstract 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- 230000002195 synergetic effect Effects 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60K—ARRANGEMENT OR MOUNTING OF PROPULSION UNITS OR OF TRANSMISSIONS IN VEHICLES; ARRANGEMENT OR MOUNTING OF PLURAL DIVERSE PRIME-MOVERS IN VEHICLES; AUXILIARY DRIVES FOR VEHICLES; INSTRUMENTATION OR DASHBOARDS FOR VEHICLES; ARRANGEMENTS IN CONNECTION WITH COOLING, AIR INTAKE, GAS EXHAUST OR FUEL SUPPLY OF PROPULSION UNITS IN VEHICLES
- B60K17/00—Arrangement or mounting of transmissions in vehicles
- B60K17/04—Arrangement or mounting of transmissions in vehicles characterised by arrangement, location or kind of gearing
- B60K17/16—Arrangement or mounting of transmissions in vehicles characterised by arrangement, location or kind of gearing of differential gearing
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Transportation (AREA)
- Mechanical Engineering (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10146591A DE10146591A1 (de) | 2001-09-21 | 2001-09-21 | Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen |
Publications (1)
Publication Number | Publication Date |
---|---|
AR037324A1 true AR037324A1 (es) | 2004-11-03 |
Family
ID=7699813
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP020103559A AR037324A1 (es) | 2001-09-21 | 2002-09-20 | Herbicidas a base de tien-3-il-sulfonilamino(tio)carbonil-triazolin(tio)onas substituidas |
ARP120104784A AR089292A2 (es) | 2001-09-21 | 2012-12-18 | Composicion herbicida a base de tien-3-il-sulfonilamino(tio)carbonil-triazolin(tio)onas substituidas, y metodos de aplicacion |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP120104784A AR089292A2 (es) | 2001-09-21 | 2012-12-18 | Composicion herbicida a base de tien-3-il-sulfonilamino(tio)carbonil-triazolin(tio)onas substituidas, y metodos de aplicacion |
Country Status (29)
Country | Link |
---|---|
US (4) | US7781374B2 (OSRAM) |
EP (19) | EP2272362B1 (OSRAM) |
JP (2) | JP4610894B2 (OSRAM) |
KR (1) | KR100955270B1 (OSRAM) |
CN (2) | CN102228057A (OSRAM) |
AR (2) | AR037324A1 (OSRAM) |
AT (4) | ATE509526T1 (OSRAM) |
AU (1) | AU2008221577B2 (OSRAM) |
BE (2) | BE2017C015I2 (OSRAM) |
BR (1) | BR0212906B1 (OSRAM) |
CA (2) | CA2699570C (OSRAM) |
CO (1) | CO5580724A2 (OSRAM) |
CY (1) | CY1113927T1 (OSRAM) |
DE (1) | DE10146591A1 (OSRAM) |
DK (16) | DK2272358T3 (OSRAM) |
ES (15) | ES2391815T3 (OSRAM) |
FR (3) | FR14C0043I2 (OSRAM) |
HR (1) | HRP20040358B1 (OSRAM) |
HU (15) | HU230040B1 (OSRAM) |
MX (1) | MXPA04002584A (OSRAM) |
NL (3) | NL350076I2 (OSRAM) |
PL (9) | PL209962B1 (OSRAM) |
PT (15) | PT2272366E (OSRAM) |
RS (1) | RS52547B (OSRAM) |
RU (1) | RU2303872C9 (OSRAM) |
SI (14) | SI2279663T1 (OSRAM) |
UA (1) | UA78229C2 (OSRAM) |
WO (1) | WO2003026426A1 (OSRAM) |
ZA (1) | ZA200402130B (OSRAM) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10146591A1 (de) * | 2001-09-21 | 2003-04-10 | Bayer Cropscience Ag | Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen |
DE10146590A1 (de) * | 2001-09-21 | 2003-04-10 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und Safenern |
DE10154074A1 (de) * | 2001-11-02 | 2003-05-15 | Bayer Cropscience Ag | Substituierte Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)one |
DE102004010812A1 (de) * | 2004-03-05 | 2005-09-22 | Bayer Cropscience Ag | Unkrautbekämpfungsverfahren |
DE102004010813A1 (de) * | 2004-03-05 | 2005-11-10 | Bayer Cropscience Ag | Neue Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyltriazolin(thi)onen und 4-HPPD-Hemmstoffen |
DE102004062541A1 (de) * | 2004-12-24 | 2006-07-06 | Bayer Cropscience Ag | Synergistische herbizide Wirkstoffkombination |
CA2630209C (en) * | 2005-11-17 | 2014-05-20 | Bayer Cropscience Ag | Aqueous herbicidal composition based on a suspension concentrate comprising herbicides and safener |
DE102006032164A1 (de) * | 2006-07-12 | 2008-01-24 | Bayer Cropscience Ag | Substituierte Furyl-sulfonylamino(thio)carbonyl-triazolin(thi)one |
GB0625589D0 (en) * | 2006-12-21 | 2007-01-31 | Agrovista Uk Ltd | Herbicide composition |
US20090215625A1 (en) * | 2008-01-07 | 2009-08-27 | Auburn University | Combinations of Herbicides and Safeners |
CN101980600A (zh) * | 2008-02-05 | 2011-02-23 | 北美爱利思达生命科学有限责任公司 | 低熔点活性化合物的固体制剂 |
US20090203526A1 (en) * | 2008-02-12 | 2009-08-13 | Arysta Lifescience North America, Llc | Method of controlling unwanted vegetation |
CN102143685B (zh) | 2008-07-03 | 2015-05-27 | 孟山都技术公司 | 作为除草剂辅助剂的衍生化糖表面活性剂和醚胺氧化物表面活性剂的组合 |
UA104598C2 (ru) * | 2008-10-06 | 2014-02-25 | Сингента Партисипейшнс Аг | Гербицидная композиция и способ ее применения |
CN102027924B (zh) * | 2009-09-28 | 2013-01-23 | 南京华洲药业有限公司 | 一种含毒莠定与麦草畏的除草组合物 |
CN102027960B (zh) * | 2009-09-28 | 2013-01-23 | 南京华洲药业有限公司 | 一种含毒莠定与异丙隆的除草组合物及其应用 |
CN102027923B (zh) * | 2009-09-28 | 2013-01-23 | 南京华洲药业有限公司 | 一种含毒莠定与二甲戊乐灵的增效除草组合物及其应用 |
CN102027971B (zh) * | 2009-09-28 | 2013-09-18 | 南京华洲药业有限公司 | 含氟吡草腙、麦草畏及烟嘧磺隆的除草剂组合物及其应用 |
RU2492647C1 (ru) * | 2012-01-27 | 2013-09-20 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Кубанский государственный технологический университет" (ФГБОУ ВПО "КубГТУ") | 2-(1н-бензимидазол-2-ил)-5'-нитробензойная кислота - антидот гербицида гормонального действия 2,4-дихлорфеноксиуксусной кислоты и способ его получения |
CN104349674A (zh) * | 2012-05-29 | 2015-02-11 | 拜尔农作物科学有限合伙人公司 | 控制杂草侵染和提高草质量的方法和组合物 |
WO2014100364A1 (en) * | 2012-12-21 | 2014-06-26 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and flurtamone |
CN105007736B (zh) | 2012-12-21 | 2018-06-29 | 美国陶氏益农公司 | 包含4-氨基-3-氯-6-(4-氯-2-氟-3-甲氧基苯基)-5-氟吡啶-2-羧酸或其衍生物和呋草酮、吡氟酰草胺、或氟吡酰草胺的除草组合物 |
DK2943066T3 (en) * | 2013-01-10 | 2018-10-29 | Dow Agrosciences Llc | PROTECTION OF 4-AMINO-3-CHLOR-6- (4-CHLOR-2-FLUOR-3-METHOXY-PHENYL) -PYRIDINE-2-CARBOXYLIC ACID AND ITS DERIVATIVES ON CORN PLANTS |
CN103210944B (zh) * | 2013-04-28 | 2014-11-05 | 江苏龙灯化学有限公司 | 一种复配除草组合物 |
UA118765C2 (uk) * | 2013-08-09 | 2019-03-11 | Байєр Кропсайєнс Акцієнгезелльшафт | Третинні гербіцидні комбінації, що містять дві сульфонілсечовини |
CN103609583B (zh) * | 2013-08-24 | 2015-02-25 | 山东滨农科技有限公司 | 一种含有氟唑磺隆的除草剂组合物 |
WO2017023515A1 (en) * | 2015-07-31 | 2017-02-09 | E. I. Du Pont De Nemours And Company | Cyclic n-carboxamide compounds useful as herbicides |
EP3222143A1 (en) | 2016-03-24 | 2017-09-27 | Bayer CropScience Aktiengesellschaft | Use of certain herbicide combinations based on iodosulfuron in teff plants |
US11565974B2 (en) | 2017-01-18 | 2023-01-31 | Evonik Operations Gmbh | Granular thermal insulation material and method for producing the same |
DE102017209782A1 (de) | 2017-06-09 | 2018-12-13 | Evonik Degussa Gmbh | Verfahren zur Wärmedämmung eines evakuierbaren Behälters |
KR102543511B1 (ko) | 2018-07-17 | 2023-06-15 | 에보니크 오퍼레이션즈 게엠베하 | 발연 실리카 과립을 기재로 하는 단열성 조성물 및 그의 제조 방법 |
MX2021000626A (es) | 2018-07-18 | 2021-03-25 | Evonik Operations Gmbh | Procedimiento de hidrofobizacion de cuerpos de material de aislamiento conformados a base de silice a presion ambiental. |
KR20220012302A (ko) * | 2019-05-24 | 2022-02-03 | 에프엠씨 코포레이션 | 제초제로서의 피라졸-치환 피롤리디논 |
CN110498922A (zh) * | 2019-08-31 | 2019-11-26 | 贵州大学 | 一种n-(4-苯胺基苯基)甲基丙烯酸甲酯与乙二胺共聚大分子抗氧剂及其应用 |
CN111097386B (zh) * | 2019-12-26 | 2022-01-11 | 江苏大学 | 一种二维层状水稳定染料吸附剂及制备方法 |
CN112841211A (zh) * | 2021-01-29 | 2021-05-28 | 广西三晶化工科技有限公司 | 甘蔗田和玉米地芽前芽后均适用的除草组合物及其应用 |
CN115536674B (zh) * | 2022-11-03 | 2024-05-31 | 青岛科技大学 | 一种哒嗪螺苯并磺内酰胺化合物及其合成方法与用途 |
WO2024200431A1 (en) | 2023-03-31 | 2024-10-03 | Bayer Aktiengesellschaft | Emulsifiable concentrate (ec) formulation with thiencarbazone-methyl |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB820180A (en) | 1956-09-18 | 1959-09-16 | Boots Pure Drug Co Ltd | New salts of alpha-(4-chloro-2-methylphenoxy)-propionic acid and herbicidal compositions containing them |
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 |
DE3680212D1 (de) | 1985-02-14 | 1991-08-22 | Ciba Geigy Ag | Verwendung von chinolinderivaten zum schuetzen von kulturpflanzen. |
JPS6372605A (ja) | 1986-09-12 | 1988-04-02 | Dainippon Ink & Chem Inc | 改良されたヒドラジン系農薬組成物 |
US5599944A (en) | 1987-03-24 | 1997-02-04 | Bayer Aktiengesellschaft | Intermediates for herbicidal sulphonylaminocarbonyltriazolinones having substituents which are bonded via sulphur |
DE3726919A1 (de) | 1987-08-13 | 1989-02-23 | Bayer Ag | 1-arylpyrazole |
US5700758A (en) | 1989-11-30 | 1997-12-23 | Hoechst Aktiengesellschaft | Pyrazolines for protecting crop plants against herbicides |
DE3939503A1 (de) | 1989-11-30 | 1991-06-06 | Hoechst Ag | Neue pyrazoline zum schutz von kulturpflanzen gegenueber herbiziden |
US5529976A (en) | 1990-01-10 | 1996-06-25 | Hoechst Aktiengesellschaft | Pyridyl sulphonyl ureas as herbicides and plant growth regulators |
WO1991010660A1 (de) | 1990-01-10 | 1991-07-25 | Hoechst Aktiengesellschaft | Pyridylsulfonylharnstoffe als herbizide und pflanzenwachstumsregulatoren, verfahren zu ihrer herstellung und ihre verwendung |
DE4039810C1 (OSRAM) | 1990-12-13 | 1991-10-17 | Mtu Muenchen Gmbh | |
IL113138A (en) * | 1994-04-22 | 1999-05-09 | Zeneca Ltd | Herbicidal composition comprising a substituted 1, 3-cyclohexanedione compound and a 2-chloro-4- ethylamino-6- isopropylamino-s- triazine and a method of use thereof |
PT758324E (pt) | 1994-05-04 | 2005-07-29 | Bayer Cropscience Ag | Tiocarboxilamidas aromaticas substituidas e sua utilizacao como herbicidas |
JP4117386B2 (ja) | 1995-02-24 | 2008-07-16 | ビーエーエスエフ ソシエタス・ヨーロピア | ピラゾリルベンゾイル誘導体 |
DE19508118A1 (de) | 1995-03-08 | 1996-09-12 | Bayer Ag | Sulfonylaminocarbonyltriazoline mit Halogenalkoxy-Substituenten |
DE19621522A1 (de) * | 1996-05-29 | 1997-12-04 | Hoechst Schering Agrevo Gmbh | Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung |
DE19638887A1 (de) * | 1996-09-23 | 1998-03-26 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
DE19650196A1 (de) * | 1996-12-04 | 1998-06-10 | Bayer Ag | Thienylsulfonylamino(thio)carbonylverbindungen |
DE59808163D1 (de) | 1997-01-17 | 2003-06-05 | Basf Ag | Verfahren zur herstellung von schwefelhaltigen 2-chlor-3-(4,5-dihydroisoxazol-3-yl)-benzoesäuren |
ES2318868T3 (es) | 1997-01-17 | 2009-05-01 | Basf Se | Derivados del benzoilo sustituidos por 3-heterociclilo. |
DE19742951A1 (de) * | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung |
AU719657B2 (en) * | 1998-01-21 | 2000-05-11 | Syngenta Participations Ag | Herbicidal composition |
DE19827855A1 (de) | 1998-06-23 | 1999-12-30 | Hoechst Schering Agrevo Gmbh | Kombinationen aus Herbiziden und Safenern |
DE19933260A1 (de) * | 1999-07-15 | 2001-01-18 | Bayer Ag | Substituierte Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)one |
DE19940860A1 (de) * | 1999-08-27 | 2001-03-01 | Bayer Ag | Selektive Herbizide auf Basis eines substituierten Phenylsulfonyl aminocarbonyltriazolinons und Safenern II |
DE19950943A1 (de) | 1999-10-22 | 2001-05-17 | Aventis Cropscience Gmbh | Synergistische herbizide Mittel enthaltend Herbizide aus der Gruppe der Hemmstoffe der Hydroxyphenylpyruvat-Dioxygenase |
DE10031825A1 (de) * | 2000-06-30 | 2002-01-10 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
DE10146591A1 (de) * | 2001-09-21 | 2003-04-10 | Bayer Cropscience Ag | Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen |
DE10146590A1 (de) * | 2001-09-21 | 2003-04-10 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und Safenern |
-
2001
- 2001-09-21 DE DE10146591A patent/DE10146591A1/de not_active Withdrawn
-
2002
- 2002-09-10 DK DK10183208.7T patent/DK2272358T3/da active
- 2002-09-10 SI SI200231002T patent/SI2279663T1/sl unknown
- 2002-09-10 AT AT02772283T patent/ATE509526T1/de active
- 2002-09-10 CN CN2011101072164A patent/CN102228057A/zh active Pending
- 2002-09-10 HU HU1400033A patent/HU230040B1/hu unknown
- 2002-09-10 EP EP10183226A patent/EP2272362B1/de not_active Expired - Lifetime
- 2002-09-10 EP EP10183205A patent/EP2272357B1/de not_active Expired - Lifetime
- 2002-09-10 ES ES10183174T patent/ES2391815T3/es not_active Expired - Lifetime
- 2002-09-10 CA CA2699570A patent/CA2699570C/en not_active Expired - Lifetime
- 2002-09-10 PL PL393125A patent/PL209962B1/pl unknown
- 2002-09-10 EP EP02772283A patent/EP1429612B1/de not_active Expired - Lifetime
- 2002-09-10 HU HU1600509A patent/HU230764B1/hu unknown
- 2002-09-10 SI SI200231008T patent/SI2272352T1/sl unknown
- 2002-09-10 PT PT10183243T patent/PT2272366E/pt unknown
- 2002-09-10 EP EP10183186A patent/EP2301352B1/de not_active Expired - Lifetime
- 2002-09-10 SI SI200230991T patent/SI2272362T1/sl unknown
- 2002-09-10 PL PL393128A patent/PL209963B1/pl unknown
- 2002-09-10 PL PL393127A patent/PL214795B1/pl unknown
- 2002-09-10 RU RU2004112215/04A patent/RU2303872C9/ru active Protection Beyond IP Right Term
- 2002-09-10 ES ES10183226T patent/ES2386876T3/es not_active Expired - Lifetime
- 2002-09-10 EP EP10183237A patent/EP2272365B1/de not_active Expired - Lifetime
- 2002-09-10 EP EP10183165A patent/EP2272351B1/de not_active Expired - Lifetime
- 2002-09-10 EP EP10183224A patent/EP2272361B1/de not_active Expired - Lifetime
- 2002-09-10 CN CN028231589A patent/CN1589101B/zh not_active Expired - Lifetime
- 2002-09-10 EP EP10183193A patent/EP2272355B1/de not_active Expired - Lifetime
- 2002-09-10 US US10/489,086 patent/US7781374B2/en not_active Expired - Lifetime
- 2002-09-10 PT PT10183214T patent/PT2272359E/pt unknown
- 2002-09-10 SI SI200231012T patent/SI2272361T1/sl unknown
- 2002-09-10 SI SI200231013T patent/SI2272358T1/sl unknown
- 2002-09-10 SI SI200231011T patent/SI2272353T1/sl unknown
- 2002-09-10 DK DK10183224.4T patent/DK2272361T3/da active
- 2002-09-10 DK DK10183200.4T patent/DK2272356T3/da active
- 2002-09-10 DK DK10183237.6T patent/DK2272365T3/da active
- 2002-09-10 EP EP10183180A patent/EP2272354B1/de not_active Expired - Lifetime
- 2002-09-10 MX MXPA04002584A patent/MXPA04002584A/es active IP Right Grant
- 2002-09-10 PT PT10183165T patent/PT2272351E/pt unknown
- 2002-09-10 EP EP10183230A patent/EP2272363A3/de not_active Withdrawn
- 2002-09-10 HU HU1600093A patent/HU230556B1/hu unknown
- 2002-09-10 EP EP10183234A patent/EP2272364B1/de not_active Expired - Lifetime
- 2002-09-10 EP EP10183243A patent/EP2272366B1/de not_active Expired - Lifetime
- 2002-09-10 HU HU1600092A patent/HU230750B1/hu active Protection Beyond IP Right Term
- 2002-09-10 PL PL393124A patent/PL214548B1/pl unknown
- 2002-09-10 PT PT10183228T patent/PT2279663E/pt unknown
- 2002-09-10 ES ES10183180T patent/ES2391816T3/es not_active Expired - Lifetime
- 2002-09-10 HU HU1400522A patent/HU230212B1/hu unknown
- 2002-09-10 WO PCT/EP2002/010103 patent/WO2003026426A1/de active Application Filing
- 2002-09-10 PT PT10183226T patent/PT2272362E/pt unknown
- 2002-09-10 EP EP10183174A patent/EP2272353B1/de not_active Expired - Lifetime
- 2002-09-10 SI SI200231007T patent/SI2272360T1/sl unknown
- 2002-09-10 PL PL393129A patent/PL209964B1/pl unknown
- 2002-09-10 SI SI200231009T patent/SI2272355T1/sl unknown
- 2002-09-10 HU HU1600510A patent/HU230763B1/hu unknown
- 2002-09-10 DK DK10183218.6T patent/DK2272360T3/da active
- 2002-09-10 DK DK10183226.9T patent/DK2272362T3/da active
- 2002-09-10 DK DK02772283.4T patent/DK1429612T3/da active
- 2002-09-10 PT PT10183174T patent/PT2272353E/pt unknown
- 2002-09-10 ES ES10183186T patent/ES2402884T3/es not_active Expired - Lifetime
- 2002-09-10 EP EP10183208A patent/EP2272358B1/de not_active Expired - Lifetime
- 2002-09-10 DK DK10183174.1T patent/DK2272353T3/da active
- 2002-09-10 ES ES10183200T patent/ES2390041T3/es not_active Expired - Lifetime
- 2002-09-10 PT PT10183170T patent/PT2272352E/pt unknown
- 2002-09-10 DK DK10183170.9T patent/DK2272352T3/da active
- 2002-09-10 PT PT10183208T patent/PT2272358E/pt unknown
- 2002-09-10 PT PT02772283T patent/PT1429612E/pt unknown
- 2002-09-10 DK DK10183193.1T patent/DK2272355T3/da active
- 2002-09-10 JP JP2003530080A patent/JP4610894B2/ja not_active Expired - Lifetime
- 2002-09-10 AT AT10183226T patent/ATE556595T1/de active
- 2002-09-10 ES ES10183214T patent/ES2386875T3/es not_active Expired - Lifetime
- 2002-09-10 CA CA2460915A patent/CA2460915C/en not_active Expired - Lifetime
- 2002-09-10 PL PL393123A patent/PL209961B1/pl unknown
- 2002-09-10 HU HU1600511A patent/HU230765B1/hu unknown
- 2002-09-10 SI SI200231000T patent/SI2272351T1/sl unknown
- 2002-09-10 ES ES10183208T patent/ES2396936T3/es not_active Expired - Lifetime
- 2002-09-10 ES ES10183228T patent/ES2391884T3/es not_active Expired - Lifetime
- 2002-09-10 EP EP10183200A patent/EP2272356B1/de not_active Expired - Lifetime
- 2002-09-10 HU HU0402121A patent/HU230143B1/hu unknown
- 2002-09-10 PL PL393122A patent/PL214624B1/pl unknown
- 2002-09-10 ES ES10183224T patent/ES2393059T3/es not_active Expired - Lifetime
- 2002-09-10 EP EP10183218A patent/EP2272360B1/de not_active Expired - Lifetime
- 2002-09-10 DK DK10183214.5T patent/DK2272359T3/da active
- 2002-09-10 ES ES10183170T patent/ES2391814T3/es not_active Expired - Lifetime
- 2002-09-10 PT PT101831931T patent/PT2272355E/pt unknown
- 2002-09-10 PL PL369529A patent/PL211863B1/pl unknown
- 2002-09-10 SI SI200231010T patent/SI2272366T1/sl unknown
- 2002-09-10 PT PT10183200T patent/PT2272356E/pt unknown
- 2002-09-10 SI SI200231023T patent/SI2301352T1/sl unknown
- 2002-09-10 PT PT10183180T patent/PT2272354E/pt unknown
- 2002-09-10 PT PT101831865T patent/PT2301352E/pt unknown
- 2002-09-10 SI SI200231006T patent/SI2272354T1/sl unknown
- 2002-09-10 EP EP10183170A patent/EP2272352B1/de not_active Expired - Lifetime
- 2002-09-10 KR KR1020047003527A patent/KR100955270B1/ko not_active Expired - Fee Related
- 2002-09-10 SI SI200230999T patent/SI2272356T1/sl unknown
- 2002-09-10 SI SI200230953T patent/SI1429612T1/sl unknown
- 2002-09-10 PT PT10183218T patent/PT2272360E/pt unknown
- 2002-09-10 ES ES10183165T patent/ES2390018T3/es not_active Expired - Lifetime
- 2002-09-10 ES ES10183243T patent/ES2391819T3/es not_active Expired - Lifetime
- 2002-09-10 DK DK10183243.4T patent/DK2272366T3/da active
- 2002-09-10 DK DK10183165.9T patent/DK2272351T3/da active
- 2002-09-10 RS YU24604A patent/RS52547B/en unknown
- 2002-09-10 EP EP10183214A patent/EP2272359B1/de not_active Expired - Lifetime
- 2002-09-10 PL PL393126A patent/PL393126A1/pl unknown
- 2002-09-10 HR HRP20040358AA patent/HRP20040358B1/hr not_active IP Right Cessation
- 2002-09-10 AT AT10183205T patent/ATE556593T1/de active
- 2002-09-10 DK DK10183228.5T patent/DK2279663T3/da active
- 2002-09-10 DK DK10183180.8T patent/DK2272354T3/da active
- 2002-09-10 ES ES10183193T patent/ES2391817T3/es not_active Expired - Lifetime
- 2002-09-10 HU HU1600514A patent/HU230715B1/hu unknown
- 2002-09-10 HU HU1600513A patent/HU230716B1/hu unknown
- 2002-09-10 HU HU1500202A patent/HU230472B1/hu unknown
- 2002-09-10 DK DK10183186.5T patent/DK2301352T3/da active
- 2002-09-10 AT AT10183214T patent/ATE556594T1/de active
- 2002-09-10 HU HU1600515A patent/HU230719B1/hu unknown
- 2002-09-10 ES ES10183218T patent/ES2391818T3/es not_active Expired - Lifetime
- 2002-09-10 PT PT10183224T patent/PT2272361E/pt unknown
- 2002-09-10 HU HU1600516A patent/HU230803B1/hu unknown
- 2002-09-10 ES ES02772283T patent/ES2366210T3/es not_active Expired - Lifetime
- 2002-09-10 BR BRPI0212906-0A patent/BR0212906B1/pt active IP Right Grant
- 2002-09-10 HU HU1600512A patent/HU230766B1/hu unknown
- 2002-09-10 EP EP10183228A patent/EP2279663B1/de not_active Expired - Lifetime
- 2002-09-20 AR ARP020103559A patent/AR037324A1/es active IP Right Grant
- 2002-10-09 UA UA20040402901A patent/UA78229C2/uk unknown
-
2004
- 2004-03-17 ZA ZA2004/02130A patent/ZA200402130B/en unknown
- 2004-04-19 CO CO04035720A patent/CO5580724A2/es active IP Right Grant
-
2008
- 2008-09-19 AU AU2008221577A patent/AU2008221577B2/en not_active Expired
-
2009
- 2009-12-24 JP JP2009292136A patent/JP2010100639A/ja active Pending
-
2010
- 2010-06-28 US US12/824,951 patent/US8268752B2/en not_active Expired - Fee Related
-
2012
- 2012-08-17 US US13/588,000 patent/US8648014B2/en not_active Expired - Lifetime
- 2012-12-18 AR ARP120104784A patent/AR089292A2/es active IP Right Grant
-
2013
- 2013-03-04 US US13/783,788 patent/US9055748B2/en not_active Expired - Lifetime
- 2013-04-11 CY CY20131100304T patent/CY1113927T1/el unknown
-
2014
- 2014-06-06 FR FR14C0043C patent/FR14C0043I2/fr active Active
-
2017
- 2017-02-02 NL NL350076C patent/NL350076I2/nl unknown
- 2017-05-23 BE BE2017C015C patent/BE2017C015I2/fr unknown
- 2017-09-20 FR FR17C1032C patent/FR17C1032I2/fr active Active
- 2017-09-20 FR FR17C1033C patent/FR17C1033I2/fr active Active
- 2017-11-15 BE BE2017C051C patent/BE2017C051I2/fr unknown
- 2017-12-07 NL NL350081C patent/NL350081I2/nl unknown
- 2017-12-07 NL NL350083C patent/NL350083I2/nl unknown
-
2018
- 2018-06-11 HU HUS1800026C patent/HUS1800026I1/hu unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR037324A1 (es) | Herbicidas a base de tien-3-il-sulfonilamino(tio)carbonil-triazolin(tio)onas substituidas | |
CO5231186A1 (es) | Herbicidas a base de n-aril-uracilos | |
AU605566B2 (en) | New substituted Triazolinones | |
EP0714602B1 (en) | Sulphonylaminophenyluracil herbicides for paddy field | |
WO1996007323A1 (de) | Selektive herbizide auf basis von aryluracilen | |
DE19638887A1 (de) | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen | |
WO2006131187A1 (de) | Ölsuspensionskonzentrat | |
KR960034198A (ko) | 피리돈술포닐우레아 화합물, 그의 제조 방법 및 그를 함유하는 제초제 | |
DE19947918A1 (de) | Selektive Herbizide auf Basis von Pyrimidin-Derivaten | |
DE19635060A1 (de) | Selektive Herbizide auf Basis von Carbamoyltriazolinonen | |
EP1221848A1 (de) | Selektive herbizide auf basis von n-aryl-triazolin(thi)onen | |
DE4437049A1 (de) | Selektive Herbizide auf Basis von Carbamoyltriazolinonen und Heteroaryloxyacetamiden | |
EP1049376B1 (de) | Selektive herbizide auf basis von n-aryl-triazolin(thi)onen und n-arylsulfonylamino(thio)carbonyl-triazolin(thi)onen | |
KR20040029033A (ko) | 테트라졸리논 유도체를 포함하는 선택적 제초제 | |
WO2005051082A1 (de) | Ölsuspensionskonzentrat | |
AR036385A1 (es) | 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 | |
DE4030063A1 (de) | Substituierte 5-alkoxy-1,2,4,-triazol-3-(thi)one | |
US7651978B2 (en) | Selective herbicides based on a substituted phenylsulphonylaminocarbonyl-triazolinone | |
AR036344A1 (es) | Composiciones herbicidas a base de arilcetonas sustituidas, uso de estas composiciones para la lucha contra el crecimiento indeseado de las plantas, metodo para la lucha contra las malezas, y procedimiento para la preparacion de las composiciones herbicidas | |
DE19635074A1 (de) | Selektive Herbizide für den Zuckerrohranbau | |
US7741246B2 (en) | Herbicide composition and weed-controlling method using the same | |
EP0784431B1 (de) | Herbizide, synergistische wirkstoffkombinationen mit 1-(2,6-dichlor-4-difluormethyl-phenyl)-5-(2-chlorpropionamido)-4-nitropyrazol | |
EP0963696A1 (en) | Herbicidal compositions | |
ZA200603584B (en) | Concentrated oily suspension |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration |