DE3040488A1 - Phenoxyphenylpropenyloxycarbonylverbindungen, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide - Google Patents
Phenoxyphenylpropenyloxycarbonylverbindungen, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizideInfo
- Publication number
- DE3040488A1 DE3040488A1 DE19803040488 DE3040488A DE3040488A1 DE 3040488 A1 DE3040488 A1 DE 3040488A1 DE 19803040488 DE19803040488 DE 19803040488 DE 3040488 A DE3040488 A DE 3040488A DE 3040488 A1 DE3040488 A1 DE 3040488A1
- Authority
- DE
- Germany
- Prior art keywords
- halogen
- formula
- compounds
- hydrogen
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- -1 PHENOXYPHENYLPROPENYLOXYCARBONYL COMPOUNDS Chemical class 0.000 title claims description 25
- 238000000034 method Methods 0.000 title claims description 7
- 238000004519 manufacturing process Methods 0.000 title description 5
- 239000000642 acaricide Substances 0.000 title description 3
- 239000002917 insecticide Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 29
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 150000002367 halogens Chemical class 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 8
- 241000238631 Hexapoda Species 0.000 claims description 7
- 230000000895 acaricidal effect Effects 0.000 claims description 6
- 125000005059 halophenyl group Chemical group 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000001735 carboxylic acids Chemical class 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 230000000749 insecticidal effect Effects 0.000 claims description 4
- 229910052717 sulfur Chemical group 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 27
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
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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 7
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- 239000007900 aqueous suspension Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
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- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241001635274 Cydia pomonella Species 0.000 description 2
- 102100035861 Cytosolic 5'-nucleotidase 1A Human genes 0.000 description 2
- 235000016623 Fragaria vesca Nutrition 0.000 description 2
- 240000009088 Fragaria x ananassa Species 0.000 description 2
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 2
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- 101000802744 Homo sapiens Cytosolic 5'-nucleotidase 1A Proteins 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 241001147398 Ostrinia nubilalis Species 0.000 description 2
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- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 241001674048 Phthiraptera Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 241000238680 Rhipicephalus microplus Species 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 241000255628 Tabanidae Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
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- 230000005764 inhibitory process Effects 0.000 description 2
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
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- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
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- PDOBSLHNWIVQJX-UHFFFAOYSA-N 1-ethenylcyclopropane-1-carboxylic acid Chemical class OC(=O)C1(C=C)CC1 PDOBSLHNWIVQJX-UHFFFAOYSA-N 0.000 description 1
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- 238000010790 dilution Methods 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 244000013123 dwarf bean Species 0.000 description 1
- 235000005489 dwarf bean Nutrition 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 201000002266 mite infestation Diseases 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- FHQKDLNFTINTBW-UHFFFAOYSA-N prop-1-ynyl carbamate Chemical compound CC#COC(N)=O FHQKDLNFTINTBW-UHFFFAOYSA-N 0.000 description 1
- CQPJLZWBXXBTJA-UHFFFAOYSA-N prop-1-ynylphosphonic acid Chemical class CC#CP(O)(O)=O CQPJLZWBXXBTJA-UHFFFAOYSA-N 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- CCBCJOPAGXYIQL-UHFFFAOYSA-M tetrabenzylazanium;chloride Chemical compound [Cl-].C=1C=CC=CC=1C[N+](CC=1C=CC=CC=1)(CC=1C=CC=CC=1)CC1=CC=CC=C1 CCBCJOPAGXYIQL-UHFFFAOYSA-M 0.000 description 1
- DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19803040488 DE3040488A1 (de) | 1980-10-28 | 1980-10-28 | Phenoxyphenylpropenyloxycarbonylverbindungen, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
| ES506409A ES506409A0 (es) | 1980-10-28 | 1981-10-21 | Procedimiento para la preparacion de compuestos fenoxifenil-propeniloxicarbonilicos |
| EP81108803A EP0050859A1 (de) | 1980-10-28 | 1981-10-23 | Phenoxyphenylpropenyloxycarbonylverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide |
| GR66367A GR74700B (enExample) | 1980-10-28 | 1981-10-26 | |
| IL64121A IL64121A0 (en) | 1980-10-28 | 1981-10-26 | Phenoxyphenylpropenyloxycarbonyl compounds,processes for their preparation and their use as insecticides and acaricides |
| ZW258/81A ZW25881A1 (en) | 1980-10-28 | 1981-10-26 | Phenoxyphenylpropenyloxycarbonyl compounds processes for their preparation and their use as insecticides and acaricides |
| US06/315,150 US4370345A (en) | 1980-10-28 | 1981-10-26 | Phenoxyphenylpropenyloxycarbonyl compounds and their use as insecticides and acaricides |
| ZA817429A ZA817429B (en) | 1980-10-28 | 1981-10-27 | Phenoxyphenylpropenyloxycarbonyl compounds,processes for their preparation and their use as insecticides and acaricides |
| JP56170848A JPS5799554A (en) | 1980-10-28 | 1981-10-27 | Phenoxyphenylpropenyloxycarbonyl compounds, manufacture and insecticidal and tickicidal agent containing same |
| BR8106952A BR8106952A (pt) | 1980-10-28 | 1981-10-27 | Compostos processo para a sua preparacao sua aplicacao composicoes inseticidas e acaricidas e processo para combater insetos e acaros nocivos |
| DK474581A DK474581A (da) | 1980-10-28 | 1981-10-27 | Phenoxyphenylpropenyloxycarbonylforbindelser fremgangsmaade til fremstilling deraf samt deres anvendelse som insecticider og acaricider |
| DD81234388A DD201752A5 (de) | 1980-10-28 | 1981-10-27 | Insektizide und akarizide mittel |
| AU76862/81A AU7686281A (en) | 1980-10-28 | 1981-10-27 | Phenoxypheny-propenyloxycarbonyl compounds |
| OA57528A OA06761A (fr) | 1980-10-28 | 1981-10-28 | Procédé phénoxyphényl-prophényloxy-carboniliques, procédé pour les préparer et leur application en tant qu'insecticides et acaricides. |
| MA19516A MA19314A1 (fr) | 1980-10-28 | 1981-10-28 | Composes phenoxyphenyl-propenyloxy-carbonyliques , procede pour les preparer et leur application en tant qu'incsecticides et acaricides . |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19803040488 DE3040488A1 (de) | 1980-10-28 | 1980-10-28 | Phenoxyphenylpropenyloxycarbonylverbindungen, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3040488A1 true DE3040488A1 (de) | 1982-06-03 |
Family
ID=6115296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19803040488 Withdrawn DE3040488A1 (de) | 1980-10-28 | 1980-10-28 | Phenoxyphenylpropenyloxycarbonylverbindungen, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4370345A (enExample) |
| EP (1) | EP0050859A1 (enExample) |
| JP (1) | JPS5799554A (enExample) |
| AU (1) | AU7686281A (enExample) |
| BR (1) | BR8106952A (enExample) |
| DD (1) | DD201752A5 (enExample) |
| DE (1) | DE3040488A1 (enExample) |
| DK (1) | DK474581A (enExample) |
| ES (1) | ES506409A0 (enExample) |
| GR (1) | GR74700B (enExample) |
| IL (1) | IL64121A0 (enExample) |
| MA (1) | MA19314A1 (enExample) |
| OA (1) | OA06761A (enExample) |
| ZA (1) | ZA817429B (enExample) |
| ZW (1) | ZW25881A1 (enExample) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4118505A (en) * | 1973-04-20 | 1978-10-03 | Sumitomo Chemical Company, Limited | Novel cyclopropanecarboxylates |
| JPS5638563B2 (enExample) * | 1973-07-28 | 1981-09-08 | ||
| US4225616A (en) * | 1978-06-26 | 1980-09-30 | Ciba-Geigy Corporation | Tetrahaloethylcyclopropane-carboxylic acid esters |
-
1980
- 1980-10-28 DE DE19803040488 patent/DE3040488A1/de not_active Withdrawn
-
1981
- 1981-10-21 ES ES506409A patent/ES506409A0/es active Granted
- 1981-10-23 EP EP81108803A patent/EP0050859A1/de not_active Withdrawn
- 1981-10-26 ZW ZW258/81A patent/ZW25881A1/xx unknown
- 1981-10-26 IL IL64121A patent/IL64121A0/xx unknown
- 1981-10-26 US US06/315,150 patent/US4370345A/en not_active Expired - Fee Related
- 1981-10-26 GR GR66367A patent/GR74700B/el unknown
- 1981-10-27 ZA ZA817429A patent/ZA817429B/xx unknown
- 1981-10-27 DD DD81234388A patent/DD201752A5/de unknown
- 1981-10-27 JP JP56170848A patent/JPS5799554A/ja active Pending
- 1981-10-27 BR BR8106952A patent/BR8106952A/pt unknown
- 1981-10-27 AU AU76862/81A patent/AU7686281A/en not_active Abandoned
- 1981-10-27 DK DK474581A patent/DK474581A/da not_active Application Discontinuation
- 1981-10-28 OA OA57528A patent/OA06761A/xx unknown
- 1981-10-28 MA MA19516A patent/MA19314A1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0050859A1 (de) | 1982-05-05 |
| ZW25881A1 (en) | 1982-05-19 |
| ES8207118A1 (es) | 1982-09-16 |
| BR8106952A (pt) | 1982-07-13 |
| DK474581A (da) | 1982-04-29 |
| AU7686281A (en) | 1982-05-06 |
| ZA817429B (en) | 1982-09-29 |
| ES506409A0 (es) | 1982-09-16 |
| JPS5799554A (en) | 1982-06-21 |
| GR74700B (enExample) | 1984-07-04 |
| OA06761A (fr) | 1982-06-30 |
| IL64121A0 (en) | 1982-01-31 |
| DD201752A5 (de) | 1983-08-10 |
| MA19314A1 (fr) | 1982-07-01 |
| US4370345A (en) | 1983-01-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8130 | Withdrawal |