UA73168C2 - Benzoilpyrazols and herbicide on the base thereof - Google Patents
Benzoilpyrazols and herbicide on the base thereof Download PDFInfo
- Publication number
- UA73168C2 UA73168C2 UA2002108642A UA2002108642A UA73168C2 UA 73168 C2 UA73168 C2 UA 73168C2 UA 2002108642 A UA2002108642 A UA 2002108642A UA 2002108642 A UA2002108642 A UA 2002108642A UA 73168 C2 UA73168 C2 UA 73168C2
- Authority
- UA
- Ukraine
- Prior art keywords
- methyl
- ethyl
- plants
- compounds
- benzoylpyrazoles
- Prior art date
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- 239000004009 herbicide Substances 0.000 title claims abstract description 22
- 230000002363 herbicidal effect Effects 0.000 title claims description 16
- UYMQWGLCXYHTES-UHFFFAOYSA-N phenyl(1h-pyrazol-5-yl)methanone Chemical class C=1C=CC=CC=1C(=O)C1=CC=NN1 UYMQWGLCXYHTES-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims description 53
- -1 benzoylmethyl Chemical group 0.000 claims description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 12
- 150000002367 halogens Chemical group 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000006418 4-methylphenylsulfonyl group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000001893 nitrooxy group Chemical group [O-][N+](=O)O* 0.000 claims description 3
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 2
- 125000006124 n-propyl sulfonyl group Chemical group 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
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- 238000009472 formulation Methods 0.000 description 18
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- 239000000843 powder Substances 0.000 description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
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- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- 108020004414 DNA Proteins 0.000 description 3
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- 239000005562 Glyphosate Substances 0.000 description 3
- 244000299507 Gossypium hirsutum Species 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 108091028043 Nucleic acid sequence Proteins 0.000 description 3
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- 240000005592 Veronica officinalis Species 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 3
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- XBYRMPXUBGMOJC-UHFFFAOYSA-N 1,2-dihydropyrazol-3-one Chemical class OC=1C=CNN=1 XBYRMPXUBGMOJC-UHFFFAOYSA-N 0.000 description 2
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 2
- OGYBDKOCZVSHQI-UHFFFAOYSA-N 2-methylsulfonyl-4-(trifluoromethyl)benzoic acid Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(O)=O OGYBDKOCZVSHQI-UHFFFAOYSA-N 0.000 description 2
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- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
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- 229920000570 polyether Polymers 0.000 description 1
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- FROBCXTULYFHEJ-OAHLLOKOSA-N propaquizafop Chemical compound C1=CC(O[C@H](C)C(=O)OCCON=C(C)C)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 FROBCXTULYFHEJ-OAHLLOKOSA-N 0.000 description 1
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- 102000004169 proteins and genes Human genes 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 description 1
- OSUHJPCHFDQAIT-GFCCVEGCSA-N quizalofop-P-ethyl Chemical group C1=CC(O[C@H](C)C(=O)OCC)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 OSUHJPCHFDQAIT-GFCCVEGCSA-N 0.000 description 1
- BBKDWPHJZANJGB-IKJXHCRLSA-N quizalofop-P-tefuryl Chemical group O=C([C@H](OC=1C=CC(OC=2N=C3C=CC(Cl)=CC3=NC=2)=CC=1)C)OCC1CCCO1 BBKDWPHJZANJGB-IKJXHCRLSA-N 0.000 description 1
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- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
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- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 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 description 1
- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
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- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical group CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
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- 239000008096 xylene Substances 0.000 description 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10016116 | 2000-03-31 | ||
| PCT/EP2001/003070 WO2001074785A1 (de) | 2000-03-31 | 2001-03-17 | Benzoylpyrazole und ihre verwendung als herbizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA73168C2 true UA73168C2 (en) | 2005-06-15 |
Family
ID=7637164
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2002108642A UA73168C2 (en) | 2000-03-31 | 2001-03-17 | Benzoilpyrazols and herbicide on the base thereof |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US6420317B1 (cs) |
| EP (1) | EP1280778B1 (cs) |
| JP (1) | JP4938954B2 (cs) |
| KR (1) | KR100752893B1 (cs) |
| CN (1) | CN1187335C (cs) |
| AR (1) | AR027989A1 (cs) |
| AT (1) | ATE334968T1 (cs) |
| AU (2) | AU2001287299B2 (cs) |
| BG (1) | BG65857B1 (cs) |
| BR (1) | BRPI0109636B1 (cs) |
| CA (1) | CA2403942C (cs) |
| CZ (1) | CZ301032B6 (cs) |
| DE (1) | DE50110620D1 (cs) |
| ES (1) | ES2269446T3 (cs) |
| HU (1) | HU228171B1 (cs) |
| IL (2) | IL151986A0 (cs) |
| MX (1) | MXPA02009567A (cs) |
| NZ (1) | NZ521642A (cs) |
| PL (1) | PL207287B1 (cs) |
| RS (1) | RS50437B (cs) |
| RU (1) | RU2276665C2 (cs) |
| SK (1) | SK285580B6 (cs) |
| TW (1) | TWI239953B (cs) |
| UA (1) | UA73168C2 (cs) |
| WO (1) | WO2001074785A1 (cs) |
| ZA (1) | ZA200207829B (cs) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20030017549A (ko) * | 2000-06-19 | 2003-03-03 | 바이엘 크롭사이언스 게엠베하 | 제초제 |
| DE10157339A1 (de) * | 2001-11-22 | 2003-06-12 | Bayer Cropscience Gmbh | Synergistische herbizide Mittel enthaltend Herbizide aus der Gruppe der Benzoylpyrazole |
| DE10157545A1 (de) | 2001-11-23 | 2003-06-12 | Bayer Cropscience Gmbh | Herbizide Mittel enthaltend Benzoylpyrazole und Safener |
| DE10160139A1 (de) * | 2001-12-07 | 2003-06-18 | Bayer Cropscience Gmbh | Synergistische herbizide Mittel enthaltend bestimmte Herbizide aus der Gruppe der Benzoylcylohexandione |
| DE10258867A1 (de) * | 2002-12-17 | 2004-07-08 | Bayer Cropscience Gmbh | Mikroemulsionskonzentrate |
| 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 |
| DE102004011007A1 (de) | 2004-03-06 | 2005-09-22 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
| US20050215433A1 (en) * | 2004-03-26 | 2005-09-29 | Benitez Francisco M | Aromatic fluid as agricultural solvent |
| DE102005014944A1 (de) | 2005-04-01 | 2006-10-05 | Bayer Cropscience Gmbh | Synergistische kulturpflanzenverträgliche herbizide Mittel enthaltend Herbizide aus der Gruppe der Benzoylpyrazole |
| EP1728430A1 (de) | 2005-06-04 | 2006-12-06 | Bayer CropScience GmbH | Herbizide Mittel |
| BRPI0611102A2 (pt) * | 2005-06-04 | 2010-08-10 | Bayer Cropscience Ag | concetrado de suspensão de óleo |
| DE102005048539A1 (de) * | 2005-10-11 | 2007-04-12 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
| WO2007059870A2 (de) * | 2005-11-25 | 2007-05-31 | Bayer Cropscience Ag | Wässrige suspensionskonzentrate aus 4-benzoylpyrazolherbiziden |
| EP1790229A1 (de) * | 2005-11-25 | 2007-05-30 | Bayer CropScience AG | Wässrige Suspensionskonzentrate aus Oxadiazolherbiziden |
| DE102005056744A1 (de) | 2005-11-29 | 2007-05-31 | Bayer Cropscience Gmbh | Flüssige Formulierungen enthaltend Dialkylsulfosuccinate und Inhibitoren der Hydroxyphenylpyruvat-Dioxygenase |
| DE102006056083A1 (de) | 2006-11-28 | 2008-05-29 | Bayer Cropscience Ag | Synergistisch wirkende und kulturpflanzenverträgliche herbizide Mittel enthaltend Herbizide aus der Gruppe der Benzoylpyrazole |
| EP2052615A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| DE102008037628A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Crop Science Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
| MX2012001245A (es) * | 2009-07-29 | 2012-04-20 | Bayer Cropscience Ag | 4-(3-alquilbenzoil)pirazoles y su uso como herbicidas. |
| CA2827159A1 (en) | 2011-02-15 | 2012-08-23 | Ruth Meissner | Synergistic combinations containing a dithiino-tetracarboxamide fungicide and a herbicide, safener or plant growth regulator |
| CA2835187A1 (en) | 2011-05-06 | 2012-11-15 | Syngenta Participations Ag | Herbicidal composition comprising pinoxaden and fluroxypyr, and methods of use thereof |
| DE102011080001A1 (de) | 2011-07-28 | 2012-10-25 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Carbamat-Insektizide als Safener |
| DE102011080004A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Carbamat-Fungizide als Safener |
| DE102011079991A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Crop Science Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Nicotinoid-Insektizide als Safener |
| DE102011080007A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Conazole- und Triazol-Fungizide als Safener |
| DE102011079997A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Corpscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Pyrazol-Insektizide als Safener |
| DE102011080020A1 (de) | 2011-07-28 | 2012-09-13 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Dicarboximid-Fungizide als Safener |
| DE102011080016A1 (de) | 2011-07-28 | 2012-10-25 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Strobilurin-Fungizide als Safener |
| DE102011080010A1 (de) | 2011-07-28 | 2012-10-25 | Bayer Cropscience Ag | Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Anilid- und Thiazol-Fungizide als Safener |
| CN103717076B (zh) | 2011-08-10 | 2016-04-13 | 拜耳知识产权股份有限公司 | 含有特定特特拉姆酸衍生物的活性化合物组合物 |
| JP6153619B2 (ja) | 2012-10-19 | 2017-06-28 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | カルボキサミド誘導体を含む活性化合物の組み合わせ |
| CN103980202B (zh) * | 2014-05-27 | 2017-01-18 | 青岛清原化合物有限公司 | 一种具有除草活性的4‑苯甲酰吡唑类化合物 |
| CN105230629B (zh) * | 2015-11-17 | 2017-04-19 | 青岛清原农冠抗性杂草防治有限公司 | 增效除草组合物 |
| CN105475316A (zh) * | 2015-12-29 | 2016-04-13 | 南京华洲药业有限公司 | 一种含磺酰草吡唑与异丙隆的混合除草剂 |
| CN105494353B (zh) * | 2015-12-29 | 2018-04-20 | 南京华洲药业有限公司 | 一种含磺酰草吡唑与嘧啶肟草醚的混合除草剂 |
| CN105494354B (zh) * | 2015-12-29 | 2018-02-16 | 南京华洲药业有限公司 | 一种含磺酰草吡唑与乙羧氟草醚的混合除草剂 |
| CN105494376A (zh) * | 2015-12-29 | 2016-04-20 | 南京华洲药业有限公司 | 一种含磺酰草吡唑与唑啉草酯的混合除草剂 |
| CN106070309B (zh) * | 2016-06-21 | 2018-06-15 | 江苏清原农冠抗性杂草防治有限公司 | 含有双唑草酮的复配除草组合物及其使用方法 |
| WO2023233400A1 (en) | 2022-05-30 | 2023-12-07 | Adama Agan Ltd. | Stabilized liquid herbicide formulation of high-load pyrasulfotole |
| WO2024116184A1 (en) | 2022-12-01 | 2024-06-06 | Adama Agan Ltd. | Process for the preparation of 2-alkylsulfonyl substituted benzoic acid derivatives |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5436648B2 (cs) | 1974-03-28 | 1979-11-10 | ||
| JPS6022713B2 (ja) | 1978-09-01 | 1985-06-03 | 三共株式会社 | ピラゾ−ル誘導体 |
| JPS61257974A (ja) * | 1985-05-11 | 1986-11-15 | Nissan Chem Ind Ltd | ピラゾ−ル誘導体，その製造方法および選択性除草剤 |
| US4744815A (en) * | 1985-05-11 | 1988-05-17 | Nissan Chemical Industries, Ltd. | 4-benzoyl-1-alkyl (alkenyl) - pyrazoles, composition containing them, herbicidal method of using them, and intermediate in their preparation |
| US4643757A (en) | 1985-05-20 | 1987-02-17 | Nissan Chemical Industries, Ltd. | Herbicidal 4-benzoyl-1-methyl-5-hydroxypyrazoles |
| JPH0828442A (ja) | 1994-07-20 | 1996-01-30 | Tokico Ltd | ポンプユニット |
| AR006793A1 (es) * | 1996-04-26 | 1999-09-29 | Ishihara Sangyo Kaisha | Compuestos pirazol o sus sales y herbicidas conteniendo los mismos |
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