HRP20020516B1 - Herbicidna kombinacija s aciliranim aminofenilsulfonil-ureama - Google Patents
Herbicidna kombinacija s aciliranim aminofenilsulfonil-ureamaInfo
- Publication number
- HRP20020516B1 HRP20020516B1 HR20020516A HRP20020516A HRP20020516B1 HR P20020516 B1 HRP20020516 B1 HR P20020516B1 HR 20020516 A HR20020516 A HR 20020516A HR P20020516 A HRP20020516 A HR P20020516A HR P20020516 B1 HRP20020516 B1 HR P20020516B1
- Authority
- HR
- Croatia
- Prior art keywords
- group
- residues
- alkoxy
- herbicides
- alkyl
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 6
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title 1
- -1 amino phenyl sulfonyl carbamide Chemical compound 0.000 title 1
- 235000013877 carbamide Nutrition 0.000 title 1
- 239000004202 carbamide Substances 0.000 title 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 241000196324 Embryophyta Species 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 239000002794 2,4-DB Substances 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
- QEGVVEOAVNHRAA-UHFFFAOYSA-N 2-chloro-6-(4,6-dimethoxypyrimidin-2-yl)sulfanylbenzoic acid Chemical compound COC1=CC(OC)=NC(SC=2C(=C(Cl)C=CC=2)C(O)=O)=N1 QEGVVEOAVNHRAA-UHFFFAOYSA-N 0.000 abstract 1
- IRCMYGHHKLLGHV-UHFFFAOYSA-N 2-ethoxy-3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl methanesulfonate Chemical compound C1=C(OS(C)(=O)=O)C=C2C(C)(C)C(OCC)OC2=C1 IRCMYGHHKLLGHV-UHFFFAOYSA-N 0.000 abstract 1
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005490 Carbetamide Substances 0.000 abstract 1
- 239000005500 Clopyralid Substances 0.000 abstract 1
- 239000005503 Desmedipham Substances 0.000 abstract 1
- QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 abstract 1
- DHWRNDJOGMTCPB-UHFFFAOYSA-N Dimefuron Chemical compound ClC1=CC(NC(=O)N(C)C)=CC=C1N1C(=O)OC(C(C)(C)C)=N1 DHWRNDJOGMTCPB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005508 Dimethachlor Substances 0.000 abstract 1
- 239000005510 Diuron Substances 0.000 abstract 1
- PTFJIKYUEPWBMS-UHFFFAOYSA-N Ethalfluralin Chemical compound CC(=C)CN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O PTFJIKYUEPWBMS-UHFFFAOYSA-N 0.000 abstract 1
- 239000005512 Ethofumesate Substances 0.000 abstract 1
- 239000005532 Flumioxazine Substances 0.000 abstract 1
- 239000005533 Fluometuron Substances 0.000 abstract 1
- 239000005579 Metamitron Substances 0.000 abstract 1
- 239000005580 Metazachlor Substances 0.000 abstract 1
- WXZVAROIGSFCFJ-UHFFFAOYSA-N N,N-diethyl-2-(naphthalen-1-yloxy)propanamide Chemical compound C1=CC=C2C(OC(C)C(=O)N(CC)CC)=CC=CC2=C1 WXZVAROIGSFCFJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005585 Napropamide Substances 0.000 abstract 1
- 239000005589 Oxasulfuron Substances 0.000 abstract 1
- 239000005590 Oxyfluorfen Substances 0.000 abstract 1
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 abstract 1
- 239000005594 Phenmedipham Substances 0.000 abstract 1
- 239000005606 Pyridate Substances 0.000 abstract 1
- JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 abstract 1
- 239000005608 Quinmerac Substances 0.000 abstract 1
- OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005628 Triflusulfuron Substances 0.000 abstract 1
- 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 1
- 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 1
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 abstract 1
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- WZJZMXBKUWKXTQ-UHFFFAOYSA-N desmedipham Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=CC=CC=2)=C1 WZJZMXBKUWKXTQ-UHFFFAOYSA-N 0.000 abstract 1
- SCCDDNKJYDZXMM-UHFFFAOYSA-N dimethachlor Chemical compound COCCN(C(=O)CCl)C1=C(C)C=CC=C1C SCCDDNKJYDZXMM-UHFFFAOYSA-N 0.000 abstract 1
- ZINJLDJMHCUBIP-UHFFFAOYSA-N ethametsulfuron-methyl Chemical group CCOC1=NC(NC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC)=N1 ZINJLDJMHCUBIP-UHFFFAOYSA-N 0.000 abstract 1
- FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 abstract 1
- RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 abstract 1
- STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 abstract 1
- NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 abstract 1
- IOXAXYHXMLCCJJ-UHFFFAOYSA-N oxetan-3-yl 2-[(4,6-dimethylpyrimidin-2-yl)carbamoylsulfamoyl]benzoate Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC2COC2)=N1 IOXAXYHXMLCCJJ-UHFFFAOYSA-N 0.000 abstract 1
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 abstract 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 abstract 1
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 abstract 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 abstract 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 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<
- A01N47/36—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
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Herbicidne kombinacije s učinkovitim sadržajem komponenata (A) i (B), naznačene time, da (A) je jedan ili više herbicida iz skupine spojeva formule (I) ili njihovih soli, u kojojR1 je vodik ili (C1-C4) alkil, R2 je vodik ili (C1-C4) alkil, R3 je vodik, (C1-C4) alkil, (C1-C4) alkoksi, (C2-C4)-alkenoksi, (C2-C4)-alkinoksi, (C3-C6) cikloalkil, pri čemu svaki od 5 potonjih navedenih ostataka nije supstituiran ili je supstituiran s jednim ili više ostataka iz skupine koju čine halogen, cijano, (C1-C4)alkoksi i (C1-C4) alkil-sulfonil, jedan od ostataka X i Y je halogen, (C1-C4) alkil, (C1-C4)alkoksi, (C1-C4) alkiltio, pri čemu svaki od tri potonja navedena ostatka nije supstituiran ili je supstituiran s jednim ili više ostataka iz skupine koju čine halogen, (C1-C4)alkoksi i (C1-C4) alkiltio, a drugi od ostataka X i Y je (C1-C4) alkil, (C1-C4) -alkoksi ili (C1-C4) alkiltio, pri čemu svaki od tri potonja navedena ostatka nije supstituiran ili je supstituiran s jednim ili više ostataka iz skupine koju čine halogen, (C1-C4) alkoksi i (C1-C4)alkiltio, Z je CH ili N, iB) je jedan ili više herbicida iz skupine spojeva, koju čine (B1) herbicidi koji su selektivno učinkoviti u nekoliko dikotilnih kultura protiv monokotilnih i dikotilnih korova, odabrani iz skupine koju čine: (B1.1) etofumesat, (B1.2) kloridazon, (B1.3) triflusulfuron, (B1.4) metamitron, (B1.5) metazaklor, (B1.6) napropamid, (B1.7) karbetamid, (B1.8) dimefuron, (B1.9) dimetaklor, (B1.10) norflurazon, (B1.11) fluometuron, (B1.12) metilarsonska kiselina, (B1.13) diuron, (B1.14) prometrin, (B1.15) trifluralin, (B1.16) sulfentrazon, (B1.17) etalfluralin, (B1.18) vernolat, (B1.19) flumioksazin, (B2) herbicidi koji su selektivno učinkoviti u nekoliko dikotilnih kultura pretežno protiv dikotilnih korova, odabrani iz skupine koju čine (B2.1) desmedifam, (B2.2) fenmedifam, (B2.3) kvinmerak, (B2.4) klopiralid, (B2.5) piridat, (B2.6) etametsulfuron-metil, (B2.7) piritiobak, (B2.8) oksifluorfen, (B2.9) fomezafen, (B2.10) flumiklorak, (B2.11) 2,4-DB, (B2.12) diklosulam, (B2.13) oksasulfuron, (B3) herbicidi koji su selektivno učinkoviti u nekoliko dikotilnih kultura pretežno protiv monokotilnih korova odabrani iz skupine koju čine (B3.1) profluazol, (B3.2) amikarbazon, (B3.3) piriftalid, (B3.4) trifloksisulfuran, (B3.5) epoholeon, (B3.6) tepraloksidim. Patent sadrži još 7 patentnih zahtjeva.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19955056A DE19955056A1 (de) | 1999-11-15 | 1999-11-15 | Herbizid-Kombination mit acylierten Aminophenylsulfonylharnstoffen |
| PCT/EP2000/011185 WO2001035742A2 (de) | 1999-11-15 | 2000-11-11 | Herbizid-kombination mit acylierten aminophenylsulfonylharnstoffen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HRP20020516A2 HRP20020516A2 (en) | 2004-08-31 |
| HRP20020516B1 true HRP20020516B1 (hr) | 2011-04-30 |
Family
ID=7929193
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20020516A HRP20020516B1 (hr) | 1999-11-15 | 2002-06-13 | Herbicidna kombinacija s aciliranim aminofenilsulfonil-ureama |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US6498126B1 (hr) |
| EP (1) | EP1231839B1 (hr) |
| JP (1) | JP5209834B2 (hr) |
| CN (1) | CN1269403C (hr) |
| AR (1) | AR026452A1 (hr) |
| AT (1) | ATE240041T1 (hr) |
| AU (1) | AU1856701A (hr) |
| BR (1) | BR0015583B1 (hr) |
| CA (1) | CA2396119C (hr) |
| CZ (1) | CZ297428B6 (hr) |
| DE (2) | DE19955056A1 (hr) |
| DK (1) | DK1231839T3 (hr) |
| ES (1) | ES2198364T3 (hr) |
| HR (1) | HRP20020516B1 (hr) |
| HU (1) | HU228805B1 (hr) |
| MX (1) | MXPA02004896A (hr) |
| PL (1) | PL200172B1 (hr) |
| PT (1) | PT1231839E (hr) |
| RS (1) | RS50489B (hr) |
| RU (1) | RU2273995C2 (hr) |
| SK (1) | SK286728B6 (hr) |
| UA (1) | UA72013C2 (hr) |
| WO (1) | WO2001035742A2 (hr) |
| ZA (1) | ZA200204713B (hr) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003024225A2 (en) * | 2001-09-20 | 2003-03-27 | Syngenta Participations Ag | Herbicidal composition |
| AR036712A1 (es) | 2001-10-03 | 2004-09-29 | Syngenta Participations Ag | Composicion herbicida |
| DE10160139A1 (de) * | 2001-12-07 | 2003-06-18 | Bayer Cropscience Gmbh | Synergistische herbizide Mittel enthaltend bestimmte Herbizide aus der Gruppe der Benzoylcylohexandione |
| DE10209478A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
| KR100960782B1 (ko) * | 2002-03-27 | 2010-06-01 | 구미아이 가가쿠 고교 가부시키가이샤 | 제초제 조성물 및 그것을 이용하는 제초방법 |
| ES2315166B1 (es) * | 2006-04-28 | 2009-12-11 | Sumitono Chemical Company, Limited | Composicion herbicida. |
| GB0625591D0 (en) * | 2006-12-21 | 2007-01-31 | Agrovista Uk Ltd | Herbicide composition |
| GB0625589D0 (en) * | 2006-12-21 | 2007-01-31 | Agrovista Uk Ltd | Herbicide composition |
| RU2672797C2 (ru) * | 2011-11-15 | 2018-11-19 | Закрытое акционерное общество Фирма "Август" | Гербицидная композиция и способ борьбы с сорными растениями в посевах культурных растений |
| CN104106584A (zh) * | 2014-01-26 | 2014-10-22 | 山东先达农化股份有限公司 | 一种玉米田复配除草剂组合物 |
| CN104230762B (zh) * | 2014-08-28 | 2016-01-13 | 青岛农业大学 | 一种含酰胺基团的苯磺酰胺类化合物及其制备和应用 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1995029899A1 (de) * | 1994-04-29 | 1995-11-09 | Hoechst Schering Agrevo Gmbh | Acylierte aminophenylsulfonylharnstoffe, verfahren zu deren herstellung und verwendung als herbizide und pflanzenwachstumsregulatoren |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0867604A (ja) * | 1994-06-23 | 1996-03-12 | Nissan Chem Ind Ltd | 除草剤組成物 |
-
1999
- 1999-11-15 DE DE19955056A patent/DE19955056A1/de not_active Withdrawn
-
2000
- 2000-11-11 AT AT00981250T patent/ATE240041T1/de active
- 2000-11-11 HU HU0203420A patent/HU228805B1/hu unknown
- 2000-11-11 JP JP2001537548A patent/JP5209834B2/ja not_active Expired - Lifetime
- 2000-11-11 CA CA2396119A patent/CA2396119C/en not_active Expired - Lifetime
- 2000-11-11 RS YUP-349/02A patent/RS50489B/sr unknown
- 2000-11-11 DK DK00981250T patent/DK1231839T3/da active
- 2000-11-11 CZ CZ20022090A patent/CZ297428B6/cs not_active IP Right Cessation
- 2000-11-11 PL PL357474A patent/PL200172B1/pl unknown
- 2000-11-11 SK SK813-2002A patent/SK286728B6/sk not_active IP Right Cessation
- 2000-11-11 EP EP00981250A patent/EP1231839B1/de not_active Expired - Lifetime
- 2000-11-11 MX MXPA02004896A patent/MXPA02004896A/es active IP Right Grant
- 2000-11-11 BR BRPI0015583-7A patent/BR0015583B1/pt active IP Right Grant
- 2000-11-11 DE DE50002219T patent/DE50002219D1/de not_active Expired - Lifetime
- 2000-11-11 ES ES00981250T patent/ES2198364T3/es not_active Expired - Lifetime
- 2000-11-11 UA UA2002064927A patent/UA72013C2/uk unknown
- 2000-11-11 RU RU2002116249/04A patent/RU2273995C2/ru active
- 2000-11-11 PT PT00981250T patent/PT1231839E/pt unknown
- 2000-11-11 AU AU18567/01A patent/AU1856701A/en not_active Abandoned
- 2000-11-11 WO PCT/EP2000/011185 patent/WO2001035742A2/de active Search and Examination
- 2000-11-11 CN CNB008173036A patent/CN1269403C/zh not_active Expired - Lifetime
- 2000-11-13 AR ARP000105977A patent/AR026452A1/es active IP Right Grant
- 2000-11-13 US US09/711,257 patent/US6498126B1/en not_active Expired - Lifetime
-
2002
- 2002-06-12 ZA ZA200204713A patent/ZA200204713B/en unknown
- 2002-06-13 HR HR20020516A patent/HRP20020516B1/hr not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1995029899A1 (de) * | 1994-04-29 | 1995-11-09 | Hoechst Schering Agrevo Gmbh | Acylierte aminophenylsulfonylharnstoffe, verfahren zu deren herstellung und verwendung als herbizide und pflanzenwachstumsregulatoren |
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