TWI233778B - Active compound combinations having insecticidal and acaricidal properties - Google Patents
Active compound combinations having insecticidal and acaricidal properties Download PDFInfo
- Publication number
- TWI233778B TWI233778B TW089119784A TW89119784A TWI233778B TW I233778 B TWI233778 B TW I233778B TW 089119784 A TW089119784 A TW 089119784A TW 89119784 A TW89119784 A TW 89119784A TW I233778 B TWI233778 B TW I233778B
- Authority
- TW
- Taiwan
- Prior art keywords
- alkyl
- crc6
- substituted
- halogen
- alkoxy
- Prior art date
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- 230000000895 acaricidal effect Effects 0.000 title claims abstract description 7
- 230000000749 insecticidal effect Effects 0.000 title claims abstract description 7
- 150000001875 compounds Chemical class 0.000 title claims description 80
- 239000000203 mixture Substances 0.000 claims abstract description 49
- 239000005557 antagonist Substances 0.000 claims abstract description 11
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 9
- 239000000556 agonist Substances 0.000 claims abstract description 4
- -1 CrC6-carbyl Chemical class 0.000 claims description 106
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 42
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 125000005843 halogen group Chemical group 0.000 claims description 21
- 230000002079 cooperative effect Effects 0.000 claims description 17
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 125000005842 heteroatom Chemical group 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
- 241001465754 Metazoa Species 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 125000004429 atom Chemical group 0.000 claims description 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 229910052757 nitrogen Chemical group 0.000 claims description 7
- 230000002195 synergetic effect Effects 0.000 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 239000002917 insecticide Substances 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 101100258328 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) crc-2 gene Proteins 0.000 claims description 5
- 230000001276 controlling effect Effects 0.000 claims description 5
- 239000000779 smoke Substances 0.000 claims description 5
- 239000004575 stone Substances 0.000 claims description 5
- 239000004606 Fillers/Extenders Substances 0.000 claims description 4
- 239000012190 activator Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
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- 244000061176 Nicotiana tabacum Species 0.000 claims description 3
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 229960001231 choline Drugs 0.000 claims description 3
- 210000004268 dentin Anatomy 0.000 claims description 3
- 125000006413 ring segment Chemical group 0.000 claims description 3
- 125000000335 thiazolyl group Chemical group 0.000 claims description 3
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000005109 alkynylthio group Chemical group 0.000 claims description 2
- 229960002715 nicotine Drugs 0.000 claims description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims description 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
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- 102000005962 receptors Human genes 0.000 claims description 2
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- 108010009685 Cholinergic Receptors Proteins 0.000 claims 3
- 102000034337 acetylcholine receptors Human genes 0.000 claims 3
- POPPVIRYGJQIOF-UHFFFAOYSA-N 2-acetyloxyethyl(trimethyl)azanium;3-(1-methylpyrrolidin-2-yl)pyridine Chemical compound CC(=O)OCC[N+](C)(C)C.CN1CCCC1C1=CC=CN=C1 POPPVIRYGJQIOF-UHFFFAOYSA-N 0.000 claims 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
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- 229940121683 Acetylcholine receptor antagonist Drugs 0.000 claims 1
- APOMZJYELVOCBK-UHFFFAOYSA-N C(C)(=N)N.N1=CC=CC(=C1)C1N(C)CCC1 Chemical compound C(C)(=N)N.N1=CC=CC(=C1)C1N(C)CCC1 APOMZJYELVOCBK-UHFFFAOYSA-N 0.000 claims 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
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- 239000000018 receptor agonist Substances 0.000 claims 1
- 229940044551 receptor antagonist Drugs 0.000 claims 1
- 239000002464 receptor antagonist Substances 0.000 claims 1
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- 125000004122 cyclic group Chemical group 0.000 abstract description 6
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 abstract description 4
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- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
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- 229910052709 silver Inorganic materials 0.000 description 1
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- 239000011775 sodium fluoride Substances 0.000 description 1
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- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- HXJNZPXGMGELDP-UHFFFAOYSA-J tin(4+);tetrabenzoate Chemical class [Sn+4].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 HXJNZPXGMGELDP-UHFFFAOYSA-J 0.000 description 1
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- 230000001988 toxicity Effects 0.000 description 1
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- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- JDLYKQWJXAQNNS-UHFFFAOYSA-L zinc;dibenzoate Chemical class [Zn+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 JDLYKQWJXAQNNS-UHFFFAOYSA-L 0.000 description 1
- MTYHLWRUYCUTPA-UHFFFAOYSA-L zinc;naphthalene-1-carboxylate Chemical compound [Zn+2].C1=CC=C2C(C(=O)[O-])=CC=CC2=C1.C1=CC=C2C(C(=O)[O-])=CC=CC2=C1 MTYHLWRUYCUTPA-UHFFFAOYSA-L 0.000 description 1
- PIAOLBVUVDXHHL-VOTSOKGWSA-N β-nitrostyrene Chemical compound [O-][N+](=O)\C=C\C1=CC=CC=C1 PIAOLBVUVDXHHL-VOTSOKGWSA-N 0.000 description 1
Classifications
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- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- 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
- A01N47/40—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides
-
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19948129A DE19948129A1 (de) | 1999-10-07 | 1999-10-07 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TWI233778B true TWI233778B (en) | 2005-06-11 |
Family
ID=7924680
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW089119784A TWI233778B (en) | 1999-10-07 | 2000-09-26 | Active compound combinations having insecticidal and acaricidal properties |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US6893651B1 (enExample) |
| EP (1) | EP1221845B1 (enExample) |
| JP (1) | JP5193410B2 (enExample) |
| KR (1) | KR100659929B1 (enExample) |
| CN (1) | CN1215768C (enExample) |
| AR (1) | AR025789A1 (enExample) |
| AT (1) | ATE243419T1 (enExample) |
| AU (1) | AU773494B2 (enExample) |
| BR (1) | BR0014610B1 (enExample) |
| CA (1) | CA2386360A1 (enExample) |
| CZ (1) | CZ20021184A3 (enExample) |
| DE (2) | DE19948129A1 (enExample) |
| DK (1) | DK1221845T3 (enExample) |
| ES (1) | ES2197117T3 (enExample) |
| HU (1) | HUP0202847A3 (enExample) |
| IL (1) | IL148546A0 (enExample) |
| MX (1) | MXPA02003497A (enExample) |
| PL (1) | PL362790A1 (enExample) |
| PT (1) | PT1221845E (enExample) |
| TR (1) | TR200200911T2 (enExample) |
| TW (1) | TWI233778B (enExample) |
| WO (1) | WO2001024634A1 (enExample) |
| ZA (1) | ZA200201807B (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19948129A1 (de) * | 1999-10-07 | 2001-04-12 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE19953775A1 (de) * | 1999-11-09 | 2001-05-10 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10024934A1 (de) * | 2000-05-19 | 2001-11-22 | Bayer Ag | Wirkstoffkombinationen mit insektiziden akariziden Eigenschaften |
| DE10353281A1 (de) * | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| DE102004001112A1 (de) * | 2004-01-07 | 2005-08-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektizide und akariziden Eigenschaften |
| WO2005094585A1 (en) * | 2004-03-16 | 2005-10-13 | Syngenta Participations Ag | Pesticidal composition and method for seed treatment |
| EP2008517A1 (de) * | 2007-06-29 | 2008-12-31 | Bayer CropScience AG | Akarizide Wirkstoffkombinationen |
| CN102548412B (zh) | 2009-10-15 | 2015-06-03 | 拜尔农作物科学股份公司 | 活性化合物结合物 |
| CN104186500A (zh) * | 2014-08-18 | 2014-12-10 | 广东中迅农科股份有限公司 | 一种含有噻嗪酮和螺螨酯的杀虫杀螨组合物 |
| CN104782647A (zh) * | 2015-03-31 | 2015-07-22 | 阮积恩 | 一种含噻虫啉和螺螨酯的杀螨组合物 |
| DE202015104873U1 (de) | 2015-09-14 | 2015-09-21 | Andreas Müller | Hänge-Bepflanzungsmatte |
Family Cites Families (70)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4531002A (en) | 1983-08-26 | 1985-07-23 | Shell Oil Company | Process for preparing insecticidal N-acyl-tetrahydro-2-nitromethylene-2H-1,3-thiazines |
| US4606862A (en) | 1983-08-26 | 1986-08-19 | Shell Oil Company | Amides of N-(3-(1-chloro-2-nitroethenylthio)propane) |
| JPH0629256B2 (ja) | 1983-10-06 | 1994-04-20 | 日本バイエルアグロケム株式会社 | ニトロメチレン−テトラヒドロピリミジン誘導体，その製法及び殺虫，殺ダニ，殺センチユウ剤 |
| JPS60172976A (ja) | 1984-02-16 | 1985-09-06 | Nippon Tokushu Noyaku Seizo Kk | ニトロメチレン誘導体，その製法及び殺虫，殺ダニ，殺センチユウ剤 |
| ZW5085A1 (en) | 1984-04-13 | 1985-09-18 | Nihon Tokushu Noyaku Seizo Kk | Nitromethylene derivatives,intermediates thereof,processes for production thereof,and insecticides |
| GB8500863D0 (en) | 1985-01-14 | 1985-02-20 | Fine Organics Ltd | Preparation of thiazine derivatives |
| US5204360A (en) | 1985-02-04 | 1993-04-20 | Nihon Bayer Agrochem K.K. | Heterocyclic compounds |
| ATE67493T1 (de) | 1985-02-04 | 1991-10-15 | Bayer Agrochem Kk | Heterocyclische verbindungen. |
| US5001138B1 (en) | 1985-02-04 | 1998-01-20 | Bayer Agrochem Kk | Heterocyclic compounds |
| JPH072736B2 (ja) | 1985-08-27 | 1995-01-18 | 日本バイエルアグロケム株式会社 | ニトロメチレン誘導体、その製法及び殺虫剤 |
| US5304324A (en) * | 1986-03-07 | 1994-04-19 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | Monodispersed glycol suspension of fine inorganic oxide particles having excellent dispersion stability |
| JPH0717621B2 (ja) | 1986-03-07 | 1995-03-01 | 日本バイエルアグロケム株式会社 | 新規ヘテロ環式化合物 |
| JPH085859B2 (ja) | 1986-07-01 | 1996-01-24 | 日本バイエルアグロケム株式会社 | 新規アルキレンジアミン類 |
| JPH07121909B2 (ja) | 1986-09-10 | 1995-12-25 | 日本バイエルアグロケム株式会社 | 新規複素環式化合物及び殺虫剤 |
| US4963574A (en) | 1987-02-24 | 1990-10-16 | Ciba-Geigy Corporation | N-cyanoisothiourea compounds useful in pest control |
| JPS63287764A (ja) | 1987-05-21 | 1988-11-24 | Nippon Tokushu Noyaku Seizo Kk | Ｎ−３−シアノベンジル−ヘテロ環式化合物及び殺虫剤 |
| JP2597095B2 (ja) | 1987-06-09 | 1997-04-02 | 日本バイエルアグロケム株式会社 | シアノアルキル―ヘテロ環式化合物を含有する殺虫剤 |
| CH673557A5 (enExample) | 1987-07-20 | 1990-03-30 | Ciba Geigy Ag | |
| DE3856183T2 (de) | 1987-08-01 | 1998-11-05 | Takeda Chemical Industries Ltd | Zwischenprodukte, ihre Herstellung und Verwendung zur Herstellung alpha-ungesättigter Amine |
| EP0306696B1 (de) | 1987-08-04 | 1994-02-16 | Ciba-Geigy Ag | Substituierte Guanidine |
| US4918086A (en) | 1987-08-07 | 1990-04-17 | Ciba-Geigy Corporation | 1-nitro-2,2-diaminoethylene derivatives |
| EP0303570A3 (de) | 1987-08-12 | 1990-11-07 | Ciba-Geigy Ag | Substituierte Isothioharnstoffe |
| NL8702059A (nl) * | 1987-09-02 | 1989-04-03 | Philips Nv | Supergeleidend lichaam. |
| JP2583429B2 (ja) | 1987-11-06 | 1997-02-19 | 日本バイエルアグロケム株式会社 | イミダゾリン類及び殺虫剤 |
| JP2884412B2 (ja) | 1988-10-21 | 1999-04-19 | 日本バイエルアグロケム株式会社 | 殺虫性シアノ化合物 |
| GB8826539D0 (en) | 1988-11-14 | 1988-12-21 | Shell Int Research | Nitromethylene compounds their preparation & their use as pesticides |
| JP2779403B2 (ja) | 1988-11-29 | 1998-07-23 | 日本バイエルアグロケム株式会社 | 殺虫性ニトロ化合物 |
| US5238949A (en) | 1988-11-29 | 1993-08-24 | Nihon Bayer Agrochem K.K. | Insecticidally active nitro pyridyl compounds |
| IE960442L (en) | 1988-12-27 | 1990-06-27 | Takeda Chemical Industries Ltd | Guanidine derivatives, their production and insecticides |
| JP2822050B2 (ja) | 1989-02-04 | 1998-11-05 | 日本バイエルアグロケム株式会社 | ２―ニトロイミノイミダゾリジン類の製法 |
| US5204359A (en) | 1989-02-13 | 1993-04-20 | Nihon Bayer Agrochem K.K. | Insecticidally active nitro compounds |
| ES2059841T3 (es) | 1989-02-13 | 1994-11-16 | Bayer Agrochem Kk | Nitro compuestos con actividad insecticida. |
| JP2610988B2 (ja) | 1989-03-09 | 1997-05-14 | 日本バイエルアグロケム 株式会社 | 新規ヘテロ環式化合物及び殺虫剤 |
| US6232309B1 (en) | 1989-03-09 | 2001-05-15 | Nihon Bayer Agrochem K.K. | Insecticidal heterocyclic compounds |
| US5304566A (en) | 1989-10-06 | 1994-04-19 | Nippon Soda Co., Ltd | Pyridine compounds which have useful insecticidal utility |
| JPH03200768A (ja) | 1989-10-24 | 1991-09-02 | Agro Kanesho Co Ltd | ニトログアニジン化合物及び殺虫剤 |
| AU628229B2 (en) | 1989-11-10 | 1992-09-10 | Agro-Kanesho Co. Ltd. | Hexahydrotriazine compounds and insecticides |
| JP2943246B2 (ja) | 1990-01-11 | 1999-08-30 | 日本曹達株式会社 | ニトロエチレン誘導体、その製造方法及び殺虫剤 |
| JP2867345B2 (ja) | 1990-01-23 | 1999-03-08 | 日本バイエルアグロケム株式会社 | 殺虫性トリフルオロアセチル誘導体 |
| JPH03246283A (ja) | 1990-02-21 | 1991-11-01 | Mitsubishi Kasei Corp | イソオキサゾール誘導体及びこれを有効成分とする殺虫剤 |
| US5180833A (en) * | 1990-03-16 | 1993-01-19 | Takeda Chemical Industries, Ltd. | Process for the preparation of chlorothiazole derivatives |
| JPH03279359A (ja) | 1990-03-27 | 1991-12-10 | Ishihara Sangyo Kaisha Ltd | ニトログアニジン誘導体、それらの製造方法及びそれらを含有する有害生物防除剤 |
| US5192778A (en) | 1990-04-03 | 1993-03-09 | Mitsui Toatsu Chemicals, Inc. | Dialkoxymethylimidazolidine derivatives, preparation thereof, insecticides containing same as an effective ingredient and intermediates therefor |
| US5264584A (en) | 1990-04-03 | 1993-11-23 | Mitsui Toatsu Chemicals, Inc. | Dialkoxymethylimidazolidine derivatives |
| IE911168A1 (en) | 1990-04-13 | 1991-10-23 | Takeda Chemical Industries Ltd | Novel intermediates for preparing guanidine derivatives,¹their preparation and use |
| JPH049371A (ja) | 1990-04-25 | 1992-01-14 | Ishihara Sangyo Kaisha Ltd | ニトロイミノ系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
| JPH05507088A (ja) | 1990-05-17 | 1993-10-14 | ユニバーシテイ・オブ・サウスカロライナ | 殺節足動物性ニトロエチレン及びニトログアニジン |
| JPH0739430B2 (ja) | 1990-07-06 | 1995-05-01 | アグロカネショウ株式会社 | 有機リン化合物、その製造法および該化合物を含有する殺虫、殺ダニ、殺線虫剤 |
| IL99161A (en) | 1990-08-17 | 1996-11-14 | Takeda Chemical Industries Ltd | History of guanidine A process for their preparation and preparations from pesticides that contain them |
| IL99576A0 (en) | 1990-10-05 | 1992-08-18 | Ciba Geigy Ag | Triazacyclohexane derivatives |
| DE4216814A1 (de) * | 1991-07-16 | 1993-01-21 | Bayer Ag | 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrofuranon- und 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrothiophenon-derivate |
| JP3042122B2 (ja) | 1991-12-26 | 2000-05-15 | 日本曹達株式会社 | Ｎ−シアノアセトアミジン誘導体の製造方法 |
| US6022871A (en) | 1992-07-22 | 2000-02-08 | Novartis Corporation | Oxadiazine derivatives |
| TW240163B (en) | 1992-07-22 | 1995-02-11 | Syngenta Participations Ag | Oxadiazine derivatives |
| JP3258502B2 (ja) | 1993-10-26 | 2002-02-18 | 三井化学株式会社 | 殺虫性テトラヒドロフラン誘導体 |
| JP2766848B2 (ja) | 1993-10-26 | 1998-06-18 | 三井化学株式会社 | フラニル系殺虫剤 |
| JP4136000B2 (ja) | 1994-06-03 | 2008-08-20 | 三井化学株式会社 | 殺虫性テトラヒドロフラン系化合物 |
| JP3722512B2 (ja) | 1995-04-20 | 2005-11-30 | 三井化学株式会社 | 殺虫性５−｛（テトラヒドロ−３−フラニル）メチル｝−４−ニトロイミノパーヒドロ−１，３，５−オキサジアジン誘導体 |
| DE19519007A1 (de) | 1995-05-24 | 1996-11-28 | Bayer Ag | Insektizide Mittel |
| ES2180786T3 (es) | 1995-06-28 | 2003-02-16 | Bayer Ag | Fenilcetoenoles 2,4,5-trisubstituidos para el empleo como pesticidas y herbicidas. |
| CN1152860C (zh) * | 1995-06-30 | 2004-06-09 | 拜尔公司 | 二烷基-卤代苯基取代的酮-烯醇 |
| CN100399898C (zh) * | 1996-04-29 | 2008-07-09 | 诺瓦蒂斯公司 | 农药组合物 |
| FR2761232B1 (fr) | 1997-03-26 | 2000-03-10 | Rhone Merieux | Procede et moyens d'eradication des puces dans les locaux habites par les petits mammiferes |
| DE19913174A1 (de) * | 1999-03-24 | 2000-09-28 | Bayer Ag | Synergistische insektizide Mischungen |
| DE19948129A1 (de) * | 1999-10-07 | 2001-04-12 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10013914A1 (de) * | 2000-03-21 | 2001-09-27 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10015310A1 (de) * | 2000-03-28 | 2001-10-04 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10018370A1 (de) * | 2000-04-14 | 2001-10-18 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10042736A1 (de) * | 2000-08-31 | 2002-03-14 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| US6526679B1 (en) * | 2001-11-19 | 2003-03-04 | Timothy P. Wood | Mounting device for commendation bars |
-
1999
- 1999-10-07 DE DE19948129A patent/DE19948129A1/de not_active Withdrawn
-
2000
- 2000-09-25 BR BRPI0014610-2A patent/BR0014610B1/pt active IP Right Grant
- 2000-09-25 WO PCT/EP2000/009323 patent/WO2001024634A1/de not_active Ceased
- 2000-09-25 TR TR2002/00911T patent/TR200200911T2/xx unknown
- 2000-09-25 ES ES00967765T patent/ES2197117T3/es not_active Expired - Lifetime
- 2000-09-25 JP JP2001527648A patent/JP5193410B2/ja not_active Expired - Lifetime
- 2000-09-25 AU AU77813/00A patent/AU773494B2/en not_active Ceased
- 2000-09-25 IL IL14854600A patent/IL148546A0/xx unknown
- 2000-09-25 DK DK00967765T patent/DK1221845T3/da active
- 2000-09-25 AT AT00967765T patent/ATE243419T1/de not_active IP Right Cessation
- 2000-09-25 PL PL00362790A patent/PL362790A1/xx not_active Application Discontinuation
- 2000-09-25 MX MXPA02003497A patent/MXPA02003497A/es active IP Right Grant
- 2000-09-25 DE DE50002673T patent/DE50002673D1/de not_active Expired - Lifetime
- 2000-09-25 CA CA002386360A patent/CA2386360A1/en not_active Abandoned
- 2000-09-25 EP EP00967765A patent/EP1221845B1/de not_active Expired - Lifetime
- 2000-09-25 CZ CZ20021184A patent/CZ20021184A3/cs unknown
- 2000-09-25 PT PT00967765T patent/PT1221845E/pt unknown
- 2000-09-25 KR KR1020027003617A patent/KR100659929B1/ko not_active Expired - Lifetime
- 2000-09-25 HU HU0202847A patent/HUP0202847A3/hu unknown
- 2000-09-25 US US10/089,989 patent/US6893651B1/en not_active Expired - Lifetime
- 2000-09-25 CN CN008138869A patent/CN1215768C/zh not_active Expired - Lifetime
- 2000-09-26 TW TW089119784A patent/TWI233778B/zh not_active IP Right Cessation
- 2000-09-27 AR ARP000105060A patent/AR025789A1/es not_active Application Discontinuation
-
2002
- 2002-03-05 ZA ZA200201807A patent/ZA200201807B/xx unknown
-
2005
- 2005-01-06 US US11/030,244 patent/US8841294B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| HUP0202847A3 (en) | 2005-03-29 |
| DE50002673D1 (de) | 2003-07-31 |
| US8841294B2 (en) | 2014-09-23 |
| CN1378423A (zh) | 2002-11-06 |
| AR025789A1 (es) | 2002-12-11 |
| EP1221845A1 (de) | 2002-07-17 |
| US20050187215A1 (en) | 2005-08-25 |
| KR100659929B1 (ko) | 2006-12-21 |
| AU773494B2 (en) | 2004-05-27 |
| DE19948129A1 (de) | 2001-04-12 |
| MXPA02003497A (es) | 2002-09-02 |
| JP5193410B2 (ja) | 2013-05-08 |
| TR200200911T2 (tr) | 2002-09-23 |
| PL362790A1 (en) | 2004-11-02 |
| CZ20021184A3 (cs) | 2002-07-17 |
| AU7781300A (en) | 2001-05-10 |
| CA2386360A1 (en) | 2001-04-12 |
| HUP0202847A2 (hu) | 2002-12-28 |
| ZA200201807B (en) | 2003-12-31 |
| EP1221845B1 (de) | 2003-06-25 |
| BR0014610B1 (pt) | 2013-05-07 |
| US6893651B1 (en) | 2005-05-17 |
| KR20020035605A (ko) | 2002-05-11 |
| JP2003510339A (ja) | 2003-03-18 |
| ATE243419T1 (de) | 2003-07-15 |
| CN1215768C (zh) | 2005-08-24 |
| BR0014610A (pt) | 2002-06-11 |
| PT1221845E (pt) | 2003-11-28 |
| IL148546A0 (en) | 2002-09-12 |
| DK1221845T3 (da) | 2003-10-13 |
| WO2001024634A1 (de) | 2001-04-12 |
| ES2197117T3 (es) | 2004-01-01 |
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