DD201561A5 - Schaedlingsbekaempfungsmittel auf der basis von phenoxybenzylestern - Google Patents

Schaedlingsbekaempfungsmittel auf der basis von phenoxybenzylestern Download PDF

Info

Publication number: DD201561A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; formula; fluoro; benzyl; compounds
Prior art date: 1981-01-31

Application number

DD82237049A

Other languages

German (de)

English (en)

Inventor

Rainer Fuchs

Heinz U Blank

Guenther Rottloff

Ingeborg Hammann

Bernhard Homeyer

Wolfgang Behrenz

Wilhelm Stendel

Original Assignee

Bayer Ag

Priority date (The priority date 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 date listed.)

1981-01-31

Filing date

1982-01-28

Publication date

1983-07-27

1982-01-28 Application filed by Bayer Ag filed Critical Bayer Ag

1983-07-27 Publication of DD201561A5 publication Critical patent/DD201561A5/de

Links

-1 phenoxyl esters Chemical class 0.000 claims description 28
238000000034 method Methods 0.000 claims description 17
239000000460 chlorine Substances 0.000 claims description 16
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 12
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 12
229910052794 bromium Chemical group 0.000 claims description 12
239000002253 acid Substances 0.000 claims description 11
229910052801 chlorine Inorganic materials 0.000 claims description 11
125000001309 chloro group Chemical group Cl* 0.000 claims description 10
150000003254 radicals Chemical group 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 7
241000607479 Yersinia pestis Species 0.000 claims description 6
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
239000000575 pesticide Substances 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
239000004606 Fillers/Extenders Substances 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000000304 alkynyl group Chemical group 0.000 claims description 2
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
230000000895 acaricidal effect Effects 0.000 abstract description 5
150000001735 carboxylic acids Chemical class 0.000 abstract description 5
230000000749 insecticidal effect Effects 0.000 abstract description 4
150000003839 salts Chemical class 0.000 abstract description 3
230000000361 pesticidal effect Effects 0.000 abstract description 2
150000001875 compounds Chemical class 0.000 description 48
238000012360 testing method Methods 0.000 description 31
238000002360 preparation method Methods 0.000 description 30
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
239000000203 mixture Substances 0.000 description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
239000002904 solvent Substances 0.000 description 22
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 21
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238000009472 formulation Methods 0.000 description 13
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
239000002689 soil Substances 0.000 description 12
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241001465754 Metazoa Species 0.000 description 11
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LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 9
239000003085 diluting agent Substances 0.000 description 9
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
WVDDGKGOMKODPV-UHFFFAOYSA-N hydroxymethyl benzene Natural products OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 8
239000000243 solution Substances 0.000 description 8
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230000000694 effects Effects 0.000 description 7
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239000013543 active substance Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
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ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
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125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000011734 sodium Chemical group 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
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125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
CHLAOFANYRDCPD-UJURSFKZSA-N (1s,3r)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carbonyl chloride Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@@H]1C(Cl)=O CHLAOFANYRDCPD-UJURSFKZSA-N 0.000 description 2
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XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 2
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JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 2
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- 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
- A01N47/02—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 no bond to a nitrogen atom
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/29—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/295—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing hydroxy or O-metal groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/63—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/52—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
- C07C47/575—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
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)
Crystallography & Structural Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

DD82237049A 1981-01-31 1982-01-28 Schaedlingsbekaempfungsmittel auf der basis von phenoxybenzylestern DD201561A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813103325 DE3103325A1 (de)	1981-01-31	1981-01-31	4-fluor-3-halophenoxy-benzylester, verfahren zu deren herstellung und deren verwendung in schaedlingsbekaempfungsmitteln sowie neue zwischenprodukte und verfahren zu deren herstellung

Publications (1)

Publication Number	Publication Date
DD201561A5 true DD201561A5 (de)	1983-07-27

Family

ID=6123764

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82237049A DD201561A5 (de)	1981-01-31	1982-01-28	Schaedlingsbekaempfungsmittel auf der basis von phenoxybenzylestern

Country Status (16)

Country	Link
EP (1)	EP0057384B1 (fr)
JP (1)	JPS57144241A (fr)
KR (1)	KR830008981A (fr)
AU (1)	AU7964782A (fr)
BR (1)	BR8200506A (fr)
CS (1)	CS227034B2 (fr)
DD (1)	DD201561A5 (fr)
DE (2)	DE3103325A1 (fr)
DK (1)	DK41282A (fr)
ES (1)	ES509185A0 (fr)
HU (1)	HU187635B (fr)
IL (1)	IL64891A0 (fr)
PH (1)	PH17475A (fr)
PL (1)	PL234876A1 (fr)
PT (1)	PT74325B (fr)
ZA (1)	ZA82579B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2512815B1 (fr) *	1981-04-16	1989-04-14	Roussel Uclaf	Nouveaux derives de l'acide cyclopropane carboxylique, leur procede de preparation, leur application a la lutte contre les parasites
FR2580633A1 (fr) *	1985-04-23	1986-10-24	Roussel Uclaf	Nouveaux derives de l'acide phenyl isobutyrique, leur procede de preparation, leur application a la lutte contre les parasites
GB8614002D0 (en) *	1986-06-09	1986-07-16	Ici Plc	Halogenated diphenyl ether derivatives
EP0311565A1 (fr) *	1987-10-06	1989-04-12	Ciba-Geigy Ag	Pesticides
CN103242196B (zh) *	2013-05-15	2016-01-27	联保作物科技有限公司	环丙烷羧酸酯类化合物、其制备方法及其应用

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2615435C2 (de) *	1976-04-09	1984-02-09	Bayer Ag, 5090 Leverkusen	Substituierte Phenoxybenzyloxycarbonylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide
DE2739854A1 (de) *	1977-09-03	1979-03-15	Bayer Ag	Fluorsubstituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
GR74446B (fr) *	1978-03-20	1984-06-28	American Cyanamid Co
US4389412A (en) *	1979-03-30	1983-06-21	Kuraray Company, Ltd.	Substituted cyclopropanecarboxylic acid esters and pesticidal compositions containing the same as active ingredient
JPS5681538A (en) *	1979-11-27	1981-07-03	Sumitomo Chem Co Ltd	Carboxylic acid ester, its preparation, and insecticide and miticide containing said compound as effective component
US4376785A (en) *	1980-06-19	1983-03-15	Sumitomo Chemical Company, Limited	Cyclopropanecarboxylates and a low fish toxic insecticide and/or acaricide containing them

1981
- 1981-01-31 DE DE19813103325 patent/DE3103325A1/de not_active Withdrawn
1982
- 1982-01-20 AU AU79647/82A patent/AU7964782A/en not_active Abandoned
- 1982-01-21 DE DE8282100404T patent/DE3260412D1/de not_active Expired
- 1982-01-21 EP EP82100404A patent/EP0057384B1/fr not_active Expired
- 1982-01-22 PT PT74325A patent/PT74325B/pt unknown
- 1982-01-25 PH PH26784A patent/PH17475A/en unknown
- 1982-01-28 IL IL64891A patent/IL64891A0/xx unknown
- 1982-01-28 CS CS82600A patent/CS227034B2/cs unknown
- 1982-01-28 DD DD82237049A patent/DD201561A5/de unknown
- 1982-01-29 ES ES509185A patent/ES509185A0/es active Granted
- 1982-01-29 ZA ZA82579A patent/ZA82579B/xx unknown
- 1982-01-29 PL PL23487682A patent/PL234876A1/xx unknown
- 1982-01-29 DK DK41282A patent/DK41282A/da not_active Application Discontinuation
- 1982-01-29 BR BR8200506A patent/BR8200506A/pt unknown
- 1982-01-29 JP JP57011942A patent/JPS57144241A/ja active Pending
- 1982-01-29 HU HU82274A patent/HU187635B/hu unknown
- 1982-02-01 KR KR1019820000410A patent/KR830008981A/ko not_active Withdrawn

Also Published As

Publication number	Publication date
EP0057384B1 (fr)	1984-07-25
ES8306469A1 (es)	1983-06-01
PL234876A1 (fr)	1982-10-11
CS227034B2 (en)	1984-04-16
ES509185A0 (es)	1983-06-01
HU187635B (en)	1986-02-28
KR830008981A (ko)	1983-12-16
AU7964782A (en)	1982-08-12
EP0057384A2 (fr)	1982-08-11
JPS57144241A (en)	1982-09-06
ZA82579B (en)	1982-12-29
DK41282A (da)	1982-08-01
PH17475A (en)	1984-09-03
BR8200506A (pt)	1982-12-07
DE3260412D1 (en)	1984-08-30
PT74325B (en)	1983-08-08
EP0057384A3 (en)	1982-10-20
DE3103325A1 (de)	1982-08-26
IL64891A0 (en)	1982-03-31
PT74325A (en)	1982-02-01

Publication	Publication Date	Title
US4275250A (en)	1981-06-23	Fluorobenzyl alcohols
EP0019787B1 (fr)	1984-03-14	Esters d'acides 2-phénylalcén-1-yl-cyclopropane carboxyliques, procédé pour leur préparation et application comme insecticides et acaricides; intermédiaires pour leur préparation
EP0001064B1 (fr)	1982-07-07	Derivés oxycarbonyles de phénoxybenzyles fluores; alcools phénoxybenzyliques fluorés et halogénures phénoxybenzyliques fluorés, procédés pour leur préparation et leur application
DE2810634A1 (de)	1979-09-20	Pentafluorbenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0022970A2 (fr)	1981-01-28	Stéréoisomères d'esters alpha-cyano-3-phénoxy-4-fluor-benzyliques de l'acide 2,2-diméthyl-3-(2,2-dichloro-vinyl)-cyclopropane carboxylique, procédé pour leur préparation et leur application comme insecticides et acaricides
EP0043492B1 (fr)	1983-10-05	Esters d'acides 1-aryl-cyclopropan-1-carboxyliques, leur préparation et leur application comme insecticides
EP0121847B1 (fr)	1987-01-14	Esters d'acides 2,2-diméthyl-3-(2-halovinyl)-cyclopropanecarboxyliques, procédé pour leur préparation et leur utilisation comme pesticides
CA1156254A (fr)	1983-11-01	4-fluoro-3-phenoxy-benzyl 3-alkene-1-yl-2,3- dimethyl-cyclopropanecarboxylates, procede de preparation et application dans la lutte contre les animaux nuisibles
EP0033160B1 (fr)	1985-05-02	Esters substitués d'acide 3-(1,2-dibromo-alkyl)-2,2-diméthyl-cyclopropan-1-carboxylique, procédé et produits intermédiaires pour leur préparation et leur utilisation comme insecticides
EP0057384B1 (fr)	1984-07-25	Esters 4-fluoro-3-halophénoxy benzyles, procédé pour leur fabrication et leur utilisation en pesticides ainsi que produits intermédiaires et procédé pour leur préparation
EP0029515B1 (fr)	1982-12-22	Benzylesters d'acide 2,2,3,3-tetraméthylpropanecarboxylique substitués par du fluor, procédé pour leur préparation et leur utilisation comme pesticides
EP0040742B1 (fr)	1983-07-13	Esters de l'acide 3-(chloro-3,3,4,4,4-pentafluoro-1-butényl)-2,2-diméthylcyclopropane carboxylique, procédé pour leur préparation et leur utilisation dans des insecticides
EP0026437B1 (fr)	1983-06-08	Esters fluorobenzyliques d'acide 3-(2,3-dichloro-3,3-difluoro-prop-1-én-1-yl)-2,2 diméthyl cyclopropane-carboxylique, procédé pour leur préparation et leur utilisation comme pesticides
EP0061114B1 (fr)	1984-12-12	Esters phénoxypyridylméthyl, procédé pour leur préparation et leur utilisation dans des compositions pesticides
DE3005722A1 (de)	1981-08-20	Trifluormethylbenzylester, verfahren zu deren herstellung und deren verwendung in schaedlingsbekaempfungsmitteln
DE2842542A1 (de)	1980-04-17	Substituierte bromostyryl-cyclopropancarbonsaeurephenoxybenzylester, verfahren zu ihrer herstellunnd ihre verwendung als insektizide und akarizide
EP0020954A1 (fr)	1981-01-07	Esters fluorés d'acides oxyalcénylcyclopropanecarboxyliques, procédé pour leur préparation, produits intermédiaires, leur préparation, insecticides et acaricides contenant les produits finals, leur préparation et leur utilisation
EP0076961A1 (fr)	1983-04-20	(6-Phénoxy-2-pyridinyl)méthyl esters d'acides vinylcyclopropane carboxyliques substitués, procédé pour leur préparation, et leur utilisation comme pesticides
DE2947209A1 (de)	1981-06-11	Fluor-substituierte spirocarbonsaeure-benzylester, verfahren zu ihrer herstellung und ihre verendung in schaedlingsbekaempfungsmitteln
DE2939661A1 (de)	1981-04-23	Substituierte (alpha)-phenyl-carbonsaeure-(3-phenoxy-benzyl)-ester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide