RU1792280C - Способ борьбы с нежелательной растительностью - Google Patents
Способ борьбы с нежелательной растительностьюInfo
- Publication number
- RU1792280C RU1792280C SU4614419A SU4614419A RU1792280C RU 1792280 C RU1792280 C RU 1792280C SU 4614419 A SU4614419 A SU 4614419A SU 4614419 A SU4614419 A SU 4614419A RU 1792280 C RU1792280 C RU 1792280C
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- hydrogen
- alkoxy
- halogen
- substituted
- Prior art date
Links
- 241000196324 Embryophyta Species 0.000 title description 6
- 238000000034 method Methods 0.000 title description 6
- 150000003217 pyrazoles Chemical class 0.000 abstract description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical group 0.000 abstract 6
- 150000002431 hydrogen Chemical group 0.000 abstract 6
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- WVANEDDSWQMDIK-UHFFFAOYSA-N 2-chloro-3-(2-methoxyethoxy)-4-methylsulfonylbenzoic acid Chemical compound COCCOC1=C(Cl)C(C(O)=O)=CC=C1S(C)(=O)=O WVANEDDSWQMDIK-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
- C07C317/46—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
-
- 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
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
-
- 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
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/24—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms having sulfone or sulfonic acid radicals in the molecule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/12—Esters of phosphoric acids with hydroxyaryl compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/65031—Five-membered rings having the nitrogen atoms in the positions 1 and 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Использование: сельское хоз йство, химический способ борьбы с сорной и нежелатель ной растительностью. Сущность изобретени : способ заключаетс в использовании новых производи ых пиразола Общей формулы t4(A) H- С/СО-2-С1-3-У-4СНз502СбН2/ С/ОН/, где А - этил или изопропил; V-2-метоксиэтокси, 2-этоксиэтокси, 2-изопропоксиэтоксй, цик- лопропилметокси, пропаргилоксй. 2-тетра- гидрофурфурилокси, 2-пиранилметокси, в количестве 0,05-0,4 кг/га, 4 табл.
Description
.Изобретение относитс к химическим способам борьбы с сорной и нежелательной растительностью. ;; /V
Известны способы борьбы с сорной растительностью в посевах культурных растег ний, основанные на. использовании производных пиразола. К ним относитс , например, способ, основанный на использовании 1-метил-4-ароилпиразолов.
.. - Однако известные способы данного типа недостаточно эффективны в отношении отдельных видов сорных растений.:
-; Целью изобретени вл етс повышение эффективности способа борьбы с сорн ками , основанного на испрльзованим произвЬднУх пйразбла.: ::; : Ниже представлены новые производные пиразола согласно изобретению, споббб их получени и примеры, иллюстрирующиетер- бицидные свойства этих соединений.. ; Пример 1, Получение 1-этил-4- 2- хлор-3-(2-метоксиэтокси)-4-(метансульфон ил)бензоил -5- гидроксипиразола (соединение 1).
Смесь 1,2 г 2-хлор-4-метансульфонил-3- (2-метоксйэтокси) бензойной кислоты, 0,3 г карбоната капм , 0,45 г 1-этил-5-гидрокси- Пирззола, 0,77 г М.М -дмциклЬгексилкарбо- диимида и 40 мл трет-амилового спирта перемешивают при 80-90°С 4-5 ч. После этого из реакционной смеси отгон ют растворитель, к остатку прибавл ют слабый водный раствор карбоната кали , добавл ют хлороформ, отдел ют водный слой, подкисл ют его концентрированной солйной кислотой и экстрагируют хлорофор- ./M OM/ Y .. : .у- : : .; - .. ; .; .. : Экстракт сушат над безводным сульфатом нёггри , отгон ют растворитель и получают конечное йёщёство, которое после перекристаллизации из этилового спирта . имеет т:1пл.159-1600С.
В услови х примера 1 получают другие сЬединейи , перечень которых представлен 6. табл. 1. ; Активные вещества используют в виде препаративных форм: смачивающихс порошков , концентратов эмульсий, гранул ч| Ч
ю to
00
о
со
N
{г с- -зогсн3,
N ОН А
Лослевсходна обработка
Таблица 3
Послеаскодова обработка
Продолжение табл.3
Т. а б и ц а 4
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17675888 | 1988-07-15 | ||
JP2603089 | 1989-02-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
RU1792280C true RU1792280C (ru) | 1993-01-30 |
Family
ID=26363753
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU4614419A RU1792280C (ru) | 1988-07-15 | 1989-07-14 | Способ борьбы с нежелательной растительностью |
SU915010216A RU2042667C1 (ru) | 1988-07-15 | 1991-12-03 | Производные 4-бензоилпиразола |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU915010216A RU2042667C1 (ru) | 1988-07-15 | 1991-12-03 | Производные 4-бензоилпиразола |
Country Status (13)
Country | Link |
---|---|
US (2) | US4986845A (ru) |
EP (1) | EP0352543B1 (ru) |
KR (1) | KR0128286B1 (ru) |
CN (1) | CN1017240B (ru) |
AT (1) | ATE112271T1 (ru) |
BR (1) | BR8903486A (ru) |
CA (1) | CA1338788C (ru) |
DE (1) | DE68918524T2 (ru) |
DK (1) | DK170439B1 (ru) |
ES (1) | ES2064388T3 (ru) |
HU (1) | HU205912B (ru) |
IL (1) | IL90819A (ru) |
RU (2) | RU1792280C (ru) |
Families Citing this family (54)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4008403A1 (de) * | 1990-03-16 | 1991-09-19 | Merck Patent Gmbh | Glykolsaeurederivate |
CA2131191A1 (en) * | 1992-03-03 | 1993-09-04 | Mitsuru Shibata | Pyrazole derivatives |
DE4311722C1 (de) * | 1993-04-08 | 1994-04-07 | Basf Ag | Verfahren zur Herstellung von Halogenmethyl-benzoylcyaniden und neue Halogenmethyl-benzoylcyanide |
AU685868B2 (en) * | 1993-11-09 | 1998-01-29 | Idemitsu Kosan Co. Ltd | Pyrazole derivatives and herbicide containing the same |
JP3478412B2 (ja) * | 1994-01-27 | 2003-12-15 | 富士写真フイルム株式会社 | ピラゾール化合物 |
WO1996016023A1 (de) * | 1994-11-24 | 1996-05-30 | Basf Aktiengesellschaft | Verfahren zur herstellung von halogenmethyl-benzoylcyaniden |
DE69627830T2 (de) * | 1995-02-13 | 2004-01-22 | Idemitsu Kosan Co. Ltd. | Pyrazol-derivate |
TR199700844T1 (xx) | 1995-02-24 | 1998-01-21 | Basf Aktiengesellschaft | Pirazolil-Benzoil T�revleri. |
DE19532312A1 (de) * | 1995-09-01 | 1997-03-06 | Basf Ag | Pyrazol-4-yl-benzoylderivate |
HU228459B1 (en) | 1997-01-17 | 2013-03-28 | Basf Ag | (3-heterocyclyl-substituted benzoyl)-pyrazole derivatives, preparation and intermediates thereof, and their use as herbicide |
AR012142A1 (es) * | 1997-03-24 | 2000-09-27 | Dow Agrosciences Llc | Compuestos de 1-alquil-4-benzoil-5-hiroxipirazol, composiciones herbicidas que los contienen; metodo para controlar vegetacion no deseada y compuestosintermediarios utiles para preparar dichos compuestos |
AR012141A1 (es) * | 1997-03-24 | 2000-09-27 | Dow Agrosciences Llc | PROCESO PARA PREPARAR 1-ALQUILO-4-(2-CLORO-3-ALCOXIBENCENO), COMPUESTOS INTERMEDIARIOS DE APLICACIoN EN DICHO PROCESO Y PROCEDIMIENTO PARA PREPARAR DICHOS COMPUESTOS INTERMEDIARIOS |
US6211403B1 (en) | 1997-03-24 | 2001-04-03 | Dow Agrosciences Llc | Process for preparing 2-chloro-3-alkoxy-4-alkylsulfonyl-benzoic acids and esters |
EP0984962B1 (de) * | 1997-05-07 | 2003-04-09 | Basf Aktiengesellschaft | Substituierte 4-benzoyl-pyrazole |
WO1998052926A2 (en) * | 1997-05-23 | 1998-11-26 | Dow Agrosciences Llc | 1-alkyl-4-benzoyl-5-hydroxypyrazole compounds and their use as herbicides |
EP1077972A1 (en) * | 1998-05-22 | 2001-02-28 | Dow AgroSciences LLC | 1-alkyl-4-[(3-oxetanyl-)benzoyl]-5-hydroxypyrazole compounds and their use as herbicides |
US6756497B1 (en) * | 1998-07-14 | 2004-06-29 | Nippon Soda Co., Ltd. | Benzoic acid derivatives and processes for the preparation thereof |
PL348888A1 (en) | 1998-12-04 | 2002-06-17 | Basf Ag | 3-(heterocyclyl)-substituted benzoylpyrazols |
DE19914140A1 (de) * | 1999-03-27 | 2000-09-28 | Bayer Ag | Substituierte Benzoylpyrazole |
DE19946853A1 (de) * | 1999-09-30 | 2001-04-05 | Bayer Ag | Substituierte Arylketone |
WO2001053275A2 (de) * | 2000-01-17 | 2001-07-26 | Bayer Aktiengesellschaft | Substituierte arylketone |
DE10037149A1 (de) * | 2000-07-29 | 2002-02-07 | Bayer Ag | Substituierte Arylketone |
DE10043074A1 (de) * | 2000-09-01 | 2002-03-14 | Aventis Cropscience Gmbh | Herbizid wirksame Benzoylcyclohexandione |
BR0209537A (pt) * | 2001-05-09 | 2004-03-09 | Bayer Cropscience Ag | Arilcetonas substituìdas |
DE10136449A1 (de) * | 2001-05-09 | 2002-11-14 | Bayer Ag | Substituierte Arylketone |
DE10138577A1 (de) * | 2001-05-21 | 2002-11-28 | Bayer Ag | Substituierte Benzoylpyrazole |
DE10206792A1 (de) * | 2002-02-19 | 2003-08-28 | Bayer Cropscience Ag | Substituierte Arylketone |
DE10209645A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Cropscience Ag | Substituierte Arylketone |
DE10235945A1 (de) | 2002-08-06 | 2004-02-19 | Bayer Cropscience Gmbh | 3-Aminocarbonyl substituierte Benzoylpyrazolone |
WO2005058037A1 (en) * | 2003-12-12 | 2005-06-30 | Syngenta Participations Ag | Picolinylpyrazoles as herbicides |
KR100643510B1 (ko) * | 2005-01-20 | 2006-11-10 | 박현문 | 반도체 장비용 대형 오링의 제조장치 및 그 성형장치에의해 제조된 대형 오링 |
AR056889A1 (es) | 2005-12-15 | 2007-10-31 | Ishihara Sangyo Kaisha | Compuestos benzoilpirazol y herbicidas que los contienen |
UA94003C2 (ru) * | 2006-11-28 | 2011-03-25 | Ишихара Санджай Кайша, Лтд. | Соединения бензоилпиразола, гербицид ha их ochobe и способ борьбы c нежелательными растениями |
JP5420169B2 (ja) * | 2006-12-27 | 2014-02-19 | 石原産業株式会社 | ベンゾイルピラゾール系化合物を含有する除草剤 |
JP5416354B2 (ja) | 2007-02-02 | 2014-02-12 | 石原産業株式会社 | ベンゾイルピラゾール系化合物を含有する除草性組成物 |
EP1980556A1 (de) | 2007-04-12 | 2008-10-15 | Bayer CropScience AG | 4-(4-Trifluormethyl-3-thiobenzoyl)pyrazole und ihre Verwendung als Herbizide |
DE102007026875A1 (de) | 2007-06-11 | 2008-12-24 | Bayer Cropscience Ag | 3-Cyclopropyl-4-(3-thiobenzoyl)pyrazole und ihre Verwendung als Herbizide |
JP5449855B2 (ja) * | 2008-05-20 | 2014-03-19 | 石原産業株式会社 | ピラゾール系化合物、それらの製造方法及びそれらを含有する除草剤 |
EP2127521A1 (de) * | 2008-05-29 | 2009-12-02 | Bayer CropScience Aktiengesellschaft | Herbizid wirksame 4-(3-Alkylsulfinylbenzoyl)pyrazole |
JP5584452B2 (ja) | 2008-12-11 | 2014-09-03 | 石原産業株式会社 | ベンゾイルピラゾール系化合物を含有する除草性組成物 |
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EP2550276A1 (en) | 2010-03-23 | 2013-01-30 | Basf Se | Substituted pyridines having herbicidal action |
US20130065760A1 (en) | 2010-03-23 | 2013-03-14 | Basf Se | Substituted Pyridines Having Herbicidal Action |
AU2011231819A1 (en) | 2010-03-23 | 2012-10-18 | Basf Se | Pyridothiazines having herbicidal action |
AR081526A1 (es) | 2010-03-23 | 2012-10-03 | Basf Se | Piridazinas sustituidas que tienen accion herbicida |
WO2011117211A1 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Substituted pyridazines having herbicidal action |
JP2013522335A (ja) | 2010-03-23 | 2013-06-13 | ビーエーエスエフ ソシエタス・ヨーロピア | 除草活性を有するピラジノチアジン |
WO2012010573A1 (de) | 2010-07-21 | 2012-01-26 | Bayer Cropscience Ag | 4-(4-halogenalkyl-3-thiobenzoyl)pyrazole und ihre verwendung als herbizide |
HUE028210T2 (en) | 2010-12-23 | 2016-12-28 | Basf Se | Pyridines with herbicidal activity |
WO2012168397A1 (en) | 2011-06-09 | 2012-12-13 | Basf Se | Substituted pyridines having herbicidal activity |
WO2012168241A1 (en) | 2011-06-09 | 2012-12-13 | Basf Se | Substituted pyrazines having herbicidal activity |
BR112014029531A2 (pt) | 2012-06-01 | 2017-06-27 | Basf Se | composto de piridina, composição e método para controlar vegetação indesejada |
CN105246900A (zh) | 2013-05-24 | 2016-01-13 | 巴斯夫欧洲公司 | 具有除草活性的取代吡啶化合物 |
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1989
- 1989-06-21 US US07/369,523 patent/US4986845A/en not_active Ceased
- 1989-06-29 CN CN89104508A patent/CN1017240B/zh not_active Expired
- 1989-06-30 CA CA000604603A patent/CA1338788C/en not_active Expired - Fee Related
- 1989-06-30 IL IL9081989A patent/IL90819A/en not_active IP Right Cessation
- 1989-07-11 AT AT89112691T patent/ATE112271T1/de not_active IP Right Cessation
- 1989-07-11 EP EP89112691A patent/EP0352543B1/en not_active Expired - Lifetime
- 1989-07-11 ES ES89112691T patent/ES2064388T3/es not_active Expired - Lifetime
- 1989-07-11 DE DE68918524T patent/DE68918524T2/de not_active Expired - Fee Related
- 1989-07-14 DK DK349289A patent/DK170439B1/da not_active IP Right Cessation
- 1989-07-14 HU HU893573A patent/HU205912B/hu not_active IP Right Cessation
- 1989-07-14 BR BR898903486A patent/BR8903486A/pt not_active Application Discontinuation
- 1989-07-14 KR KR1019890010068A patent/KR0128286B1/ko not_active IP Right Cessation
- 1989-07-14 RU SU4614419A patent/RU1792280C/ru active
-
1991
- 1991-12-03 RU SU915010216A patent/RU2042667C1/ru not_active IP Right Cessation
-
1992
- 1992-09-18 US US07/946,900 patent/USRE34779E/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
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Патент JP № 60-51.175, кл. А 01 N 43/56, 1985. . Л:1;;:,4 ;,,.. :. . . : v. : . * |
Also Published As
Publication number | Publication date |
---|---|
HUT51256A (en) | 1990-04-28 |
DK170439B1 (da) | 1995-09-04 |
EP0352543A1 (en) | 1990-01-31 |
IL90819A (en) | 1994-06-24 |
AU618609B2 (en) | 1992-01-02 |
DK349289D0 (da) | 1989-07-14 |
DK349289A (da) | 1990-01-16 |
EP0352543B1 (en) | 1994-09-28 |
HU205912B (en) | 1992-07-28 |
US4986845A (en) | 1991-01-22 |
CA1338788C (en) | 1996-12-10 |
RU2042667C1 (ru) | 1995-08-27 |
BR8903486A (pt) | 1990-03-13 |
AU3800589A (en) | 1990-01-25 |
CN1039586A (zh) | 1990-02-14 |
IL90819A0 (en) | 1990-01-18 |
USRE34779E (en) | 1994-11-08 |
ATE112271T1 (de) | 1994-10-15 |
ES2064388T3 (es) | 1995-02-01 |
DE68918524D1 (de) | 1994-11-03 |
DE68918524T2 (de) | 1995-05-04 |
KR900001657A (ko) | 1990-02-27 |
CN1017240B (zh) | 1992-07-01 |
KR0128286B1 (ko) | 1998-04-02 |
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