PH26000A - 3 (2H) pyridazinone compounds derivatives and compositions for controlling and/or preventing insect pests intermediates - Google Patents
3 (2H) pyridazinone compounds derivatives and compositions for controlling and/or preventing insect pests intermediates Download PDFInfo
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- PH26000A PH26000A PH37289A PH37289A PH26000A PH 26000 A PH26000 A PH 26000A PH 37289 A PH37289 A PH 37289A PH 37289 A PH37289 A PH 37289A PH 26000 A PH26000 A PH 26000A
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- 239000000203 mixture Substances 0.000 title claims description 76
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical class OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 title description 46
- 241000238631 Hexapoda Species 0.000 title description 11
- 241000607479 Yersinia pestis Species 0.000 title description 10
- 239000000543 intermediate Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 206
- 125000004432 carbon atom Chemical group C* 0.000 claims description 34
- 125000005843 halogen group Chemical group 0.000 claims description 25
- 239000004480 active ingredient Substances 0.000 claims description 21
- -1 pyridazinone compound Chemical class 0.000 claims description 18
- 230000000749 insecticidal effect Effects 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 241000238876 Acari Species 0.000 claims description 9
- 230000000895 acaricidal effect Effects 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 230000001069 nematicidal effect Effects 0.000 claims description 7
- 230000003071 parasitic effect Effects 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 4
- 125000001188 haloalkyl group Chemical group 0.000 claims description 4
- 235000013350 formula milk Nutrition 0.000 claims 9
- 239000000460 chlorine Substances 0.000 description 1503
- 125000001309 chloro group Chemical group Cl* 0.000 description 320
- 125000001246 bromo group Chemical group Br* 0.000 description 217
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 88
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 79
- 101150065749 Churc1 gene Proteins 0.000 description 79
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- 125000006414 CCl Chemical group ClC* 0.000 description 52
- 239000000243 solution Substances 0.000 description 43
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 41
- 238000000034 method Methods 0.000 description 41
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 39
- 238000009472 formulation Methods 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
- 101001122499 Homo sapiens Nociceptin receptor Proteins 0.000 description 26
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- 239000008187 granular material Substances 0.000 description 23
- 238000002360 preparation method Methods 0.000 description 23
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 21
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- 238000006243 chemical reaction Methods 0.000 description 11
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 11
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- 125000003963 dichloro group Chemical group Cl* 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
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- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 9
- 239000004563 wettable powder Substances 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
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- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 8
- 235000013312 flour Nutrition 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical compound C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 description 8
- 229910000027 potassium carbonate Inorganic materials 0.000 description 8
- 229940093956 potassium carbonate Drugs 0.000 description 8
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- 241000721621 Myzus persicae Species 0.000 description 7
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- 235000012216 bentonite Nutrition 0.000 description 7
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
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- 125000001424 substituent group Chemical group 0.000 description 6
- 239000000454 talc Substances 0.000 description 6
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- 235000015099 wheat brans Nutrition 0.000 description 6
- 241000358422 Nephotettix cincticeps Species 0.000 description 5
- 244000046052 Phaseolus vulgaris Species 0.000 description 5
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 5
- 241000500437 Plutella xylostella Species 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 5
- 229910052794 bromium Inorganic materials 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- WZPMZMCZAGFKOC-UHFFFAOYSA-N diisopropyl hydrogen phosphate Chemical compound CC(C)OP(O)(=O)OC(C)C WZPMZMCZAGFKOC-UHFFFAOYSA-N 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- 239000000230 xanthan gum Substances 0.000 description 5
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- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 4
- 241000238657 Blattella germanica Species 0.000 description 4
- 240000007124 Brassica oleracea Species 0.000 description 4
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 4
- 241000726760 Cadra cautella Species 0.000 description 4
- 241000256059 Culex pipiens Species 0.000 description 4
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
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- 150000001298 alcohols Chemical class 0.000 description 4
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- 150000007529 inorganic bases Chemical class 0.000 description 4
- 125000000466 oxiranyl group Chemical group 0.000 description 4
- 229960005235 piperonyl butoxide Drugs 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 125000005916 2-methylpentyl group Chemical group 0.000 description 3
- 125000004938 5-pyridyl group Chemical group N1=CC=CC(=C1)* 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 102100023702 C-C motif chemokine 13 Human genes 0.000 description 3
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 3
- 229940126062 Compound A Drugs 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 3
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- 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 2
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- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen 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
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having 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
- C07D237/14—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having 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
- C07D237/14—Oxygen atoms
- C07D237/16—Two oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having 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
- C07D237/18—Sulfur atoms
-
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
- C07D405/14—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 three or more hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth 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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19128987 | 1987-07-30 | ||
JP31933687 | 1987-12-17 | ||
JP63154329A JP2674102B2 (ja) | 1987-07-30 | 1988-06-22 | ピリダジノン誘導体および害虫防除剤 |
Publications (1)
Publication Number | Publication Date |
---|---|
PH26000A true PH26000A (en) | 1992-01-29 |
Family
ID=27320646
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PH37289A PH26000A (en) | 1987-07-30 | 1988-07-26 | 3 (2H) pyridazinone compounds derivatives and compositions for controlling and/or preventing insect pests intermediates |
Country Status (18)
Country | Link |
---|---|
US (1) | US4945091A (xx) |
EP (1) | EP0302346B1 (xx) |
CN (2) | CN1022563C (xx) |
AU (1) | AU618014B2 (xx) |
BG (1) | BG48201A3 (xx) |
BR (1) | BR8803774A (xx) |
CA (1) | CA1331988C (xx) |
DE (1) | DE3852587T2 (xx) |
ES (1) | ES2065901T3 (xx) |
HU (1) | HU204666B (xx) |
IE (1) | IE66308B1 (xx) |
IL (1) | IL87128A (xx) |
IN (1) | IN169817B (xx) |
NZ (1) | NZ225623A (xx) |
PH (1) | PH26000A (xx) |
PL (1) | PL155678B1 (xx) |
RU (1) | RU2033992C1 (xx) |
YU (1) | YU145988A (xx) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR244212A1 (es) * | 1986-02-08 | 1993-10-29 | Nissan Chemical Ind Ltd | Derivados de 2-t-butil-4-halo-5-fenoxi,alcoxi o alquiltio-3-(2h)-piridazinona,preparacion y composiciones de uso agricola, salvo cuando sean de aplicacion en el hombre y animales domesticos. |
US5004744A (en) * | 1988-12-13 | 1991-04-02 | Bayer Aktiengesellschaft | Pyridazinones as pesticides |
DE3844227A1 (de) * | 1988-12-29 | 1990-07-05 | Basf Ag | 3(2h)-pyridazinonderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen |
DE3914337A1 (de) * | 1989-04-29 | 1990-10-31 | Basf Ag | 3(2h)-pyridazinonderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen |
IL94394A (en) * | 1989-05-17 | 1994-10-21 | Nissan Chemical Ind Ltd | History of pyridazinone, process for their preparation and preparations for controlling and / or preventing insects, mites, nematodes and mollusks |
US5278163A (en) * | 1989-05-17 | 1994-01-11 | Nissan Chemical Industries, Ltd. | Pyridazinone derivatives and compositions for controlling and/or preventing insect pests |
FR2648135B1 (fr) * | 1989-06-07 | 1991-09-27 | Pf Medicament | Derives de phenyl-1-dihydro-1,4 amino-3 oxo-4 pyridazines, leur preparation et leur application en therapeutique |
DE4012338A1 (de) * | 1990-04-18 | 1991-10-24 | Bayer Ag | Substituierte pyridazinone, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel |
US5286725A (en) * | 1990-09-17 | 1994-02-15 | Ministero Dell'universita' E Della Ricerca Scientifica E Technologica | Pyridazinones endowed with acaricide and insecticide action |
WO1994012479A1 (en) * | 1992-12-03 | 1994-06-09 | Otsuka Kagaku Kabushiki Kaisha | Pyridazinone derivative and insecticidal and miticidal agent |
EP0665223A1 (en) * | 1994-01-28 | 1995-08-02 | Takeda Chemical Industries, Ltd. | Antitumor agent, novel 3(2H)-pyridazinone derivatives and their preparation |
MX2009002081A (es) | 2009-02-24 | 2009-10-14 | Mezclas Y Fertilizantes S A De | Una composicion de repelente botanico a base de allium sativum y acidos humicos para combatir insectos plaga y procedimiento de obtencion y usos. |
CN107964007B (zh) * | 2016-10-20 | 2021-02-12 | 沈阳中化农药化工研发有限公司 | 哒嗪酮类化合物及其应用 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2628181A (en) * | 1949-04-13 | 1953-02-10 | Monsanto Chemicals | Treating plants with 4, 5-dichloro-3-pyridazones |
US2832780A (en) * | 1955-09-14 | 1958-04-29 | Warner Lambert Pharmaceutical | Hydrazides of pyridazonyl-substituted alkanoic acids |
US3108103A (en) * | 1960-01-29 | 1963-10-22 | Basf Ag | 4, 5-dihalogenpyridazones |
BE627826A (xx) * | 1960-09-09 | |||
DE1225651B (de) * | 1961-07-19 | 1966-09-29 | Basf Ag | Verfahren zur Herstellung von 1,4,5-trisubstituierten Pyridazonen-(6) |
ES355900A1 (es) * | 1968-06-27 | 1969-12-16 | Inst De Investigaciones Terape | Procedimiento para la obtencion de compuestos de la serie de la piridazona. |
US4147784A (en) * | 1978-03-24 | 1979-04-03 | The Dow Chemical Company | 4,5-Dihydro-4-oxo-1,3-dithiolo(4,5-D)pyridazine-2-ylidene-propanedinitriles |
DE3143303A1 (de) * | 1981-10-31 | 1983-05-11 | Basf Ag, 6700 Ludwigshafen | Pyridazinon-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
US4571397A (en) * | 1982-03-05 | 1986-02-18 | Nissan Chemical Industries | Pyridazinone derivatives, preparation thereof, and agricultural and horticultural fungicidal, insecticidal, acaricidal, nematicidal compositions containing said derivatives |
DE3328770A1 (de) * | 1983-08-10 | 1985-02-28 | Basf Ag, 6700 Ludwigshafen | Pyridazinon-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
DE3578304D1 (de) * | 1984-11-29 | 1990-07-26 | Nissan Chemical Ind Ltd | Pyridazinonderivate, deren herstellung und insektizidische, acaricidische, nematicidische, fungizidische zusammensetzungen. |
JPH0641454B2 (ja) * | 1985-02-27 | 1994-06-01 | 日産化学工業株式会社 | ピリダジノン誘導体 |
US4837217A (en) * | 1985-04-19 | 1989-06-06 | Nissan Chemical Industries, Ltd. | Pyridazinone derivatives, preparation thereof, and insecticidal, acaricidal, nematicidal, fungicidal compositions |
-
1988
- 1988-07-12 US US07/217,664 patent/US4945091A/en not_active Expired - Fee Related
- 1988-07-15 IL IL8712888A patent/IL87128A/en not_active IP Right Cessation
- 1988-07-25 EP EP88111950A patent/EP0302346B1/en not_active Expired - Lifetime
- 1988-07-25 DE DE3852587T patent/DE3852587T2/de not_active Expired - Fee Related
- 1988-07-25 ES ES88111950T patent/ES2065901T3/es not_active Expired - Lifetime
- 1988-07-26 PH PH37289A patent/PH26000A/en unknown
- 1988-07-27 BG BG085065A patent/BG48201A3/xx unknown
- 1988-07-27 IN IN639/DEL/88A patent/IN169817B/en unknown
- 1988-07-28 CA CA000573355A patent/CA1331988C/en not_active Expired - Fee Related
- 1988-07-28 YU YU01459/88A patent/YU145988A/xx unknown
- 1988-07-29 RU SU884356230A patent/RU2033992C1/ru active
- 1988-07-29 BR BR8803774A patent/BR8803774A/pt not_active Application Discontinuation
- 1988-07-29 IE IE233088A patent/IE66308B1/en not_active IP Right Cessation
- 1988-07-29 PL PL1988273980A patent/PL155678B1/pl unknown
- 1988-07-29 HU HU884037A patent/HU204666B/hu not_active IP Right Cessation
- 1988-07-29 NZ NZ225623A patent/NZ225623A/xx unknown
- 1988-07-29 AU AU20195/88A patent/AU618014B2/en not_active Ceased
- 1988-07-30 CN CN88104699A patent/CN1022563C/zh not_active Expired - Fee Related
-
1991
- 1991-12-04 CN CN91111402A patent/CN1062636A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
CN1062636A (zh) | 1992-07-15 |
IL87128A (en) | 1994-06-24 |
PL273980A1 (en) | 1989-12-27 |
CN1022563C (zh) | 1993-10-27 |
EP0302346A2 (en) | 1989-02-08 |
DE3852587D1 (de) | 1995-02-09 |
IN169817B (xx) | 1991-12-28 |
DE3852587T2 (de) | 1995-05-18 |
HUT47794A (en) | 1989-04-28 |
BR8803774A (pt) | 1989-02-21 |
HU204666B (en) | 1992-02-28 |
YU145988A (en) | 1990-06-30 |
RU2033992C1 (ru) | 1995-04-30 |
AU618014B2 (en) | 1991-12-12 |
ES2065901T3 (es) | 1995-03-01 |
CN1030913A (zh) | 1989-02-08 |
EP0302346B1 (en) | 1994-12-28 |
IE66308B1 (en) | 1995-12-27 |
AU2019588A (en) | 1989-02-02 |
EP0302346A3 (en) | 1990-04-25 |
BG48201A3 (en) | 1990-12-14 |
PL155678B1 (pl) | 1991-12-31 |
IE882330L (en) | 1989-01-30 |
IL87128A0 (en) | 1988-12-30 |
NZ225623A (en) | 1990-08-28 |
CA1331988C (en) | 1994-09-13 |
US4945091A (en) | 1990-07-31 |
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