DK168287B1 - Vinylcyclopropancarboxylsyreestre, deres fremstilling og anvendelse som plantebeskyttelsesmiddel, middel heraf og fremgangsmåde til fremstilling deraf og fremgangsmåde til bekæmpelse af skadelige organismer - Google Patents

Vinylcyclopropancarboxylsyreestre, deres fremstilling og anvendelse som plantebeskyttelsesmiddel, middel heraf og fremgangsmåde til fremstilling deraf og fremgangsmåde til bekæmpelse af skadelige organismer Download PDF

Info

Publication number: DK168287B1
Authority: DK; Denmark
Prior art keywords: formula; carboxylic acid; spp; acid esters; general formula
Prior art date: 1985-04-18

Application number

DK176086A

Other languages

Danish (da)

English (en)

Other versions

DK176086A (da

DK176086D0 (da

Inventor

Klaus Naumann

Rudolf Braden

Wolfgang Behrenz

Benedikt Becker

Bernhard Homeyer

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.)

1985-04-18

Filing date

1986-04-17

Publication date

1994-03-07

1986-04-17 Application filed by Bayer Ag filed Critical Bayer Ag

1986-04-17 Publication of DK176086D0 publication Critical patent/DK176086D0/da

1986-10-19 Publication of DK176086A publication Critical patent/DK176086A/da

1994-03-07 Application granted granted Critical

1994-03-07 Publication of DK168287B1 publication Critical patent/DK168287B1/da

Links

238000002360 preparation method Methods 0.000 title claims description 20
PDOBSLHNWIVQJX-UHFFFAOYSA-N 1-ethenylcyclopropane-1-carboxylic acid Chemical class OC(=O)C1(C=C)CC1 PDOBSLHNWIVQJX-UHFFFAOYSA-N 0.000 title claims description 16
238000000034 method Methods 0.000 title claims description 14
239000003795 chemical substances by application Substances 0.000 title claims description 7
239000011814 protection agent Substances 0.000 title 1
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241000908127 Porcellio scaber Species 0.000 description 1
108010009736 Protein Hydrolysates Proteins 0.000 description 1
235000005805 Prunus cerasus Nutrition 0.000 description 1
241000722234 Pseudococcus Species 0.000 description 1
241000526145 Psylla Species 0.000 description 1
241001105129 Ptinus Species 0.000 description 1
241001509970 Reticulitermes <genus> Species 0.000 description 1
241000722249 Rhodnius prolixus Species 0.000 description 1
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241000509416 Sarcoptes Species 0.000 description 1
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241000522594 Scorpio maurus Species 0.000 description 1
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239000004113 Sepiolite Substances 0.000 description 1
241000258242 Siphonaptera Species 0.000 description 1
241000254181 Sitophilus Species 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
241000256248 Spodoptera Species 0.000 description 1
241000256247 Spodoptera exigua Species 0.000 description 1
241000256251 Spodoptera frugiperda Species 0.000 description 1
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241000130771 Tinea pellionella Species 0.000 description 1
241000333689 Tineola Species 0.000 description 1
241000511627 Tipula paludosa Species 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
241000018137 Trialeurodes vaporariorum Species 0.000 description 1
241001414833 Triatoma Species 0.000 description 1
241000254086 Tribolium <beetle> Species 0.000 description 1
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241000255993 Trichoplusia ni Species 0.000 description 1
241000267823 Trogoderma Species 0.000 description 1
241001274788 Viteus vitifoliae Species 0.000 description 1
235000013447 Xanthosoma atrovirens Nutrition 0.000 description 1
240000001781 Xanthosoma sagittifolium Species 0.000 description 1
241000353223 Xenopsylla cheopis Species 0.000 description 1
241001466337 Yponomeuta Species 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
241001414985 Zygentoma Species 0.000 description 1
KUASAUZPUNOVSE-UHFFFAOYSA-N [4-(dimethylamino)-2,3,5,6-tetrafluorophenyl]methanol Chemical compound CN(C)C1=C(F)C(F)=C(CO)C(F)=C1F KUASAUZPUNOVSE-UHFFFAOYSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000002969 artificial stone Substances 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
150000003938 benzyl alcohols Chemical class 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
239000001273 butane Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
229940105329 carboxymethylcellulose Drugs 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
NSRVAAFSPOGUEI-UHFFFAOYSA-N chloro-(2,3,5,6-tetrafluoro-4-methylphenyl)methanethiol Chemical compound CC1=C(F)C(F)=C(C(S)Cl)C(F)=C1F NSRVAAFSPOGUEI-UHFFFAOYSA-N 0.000 description 1
XLOPRKKSAJMMEW-UHFFFAOYSA-N chrysanthemic acid Chemical compound CC(C)=CC1C(C(O)=O)C1(C)C XLOPRKKSAJMMEW-UHFFFAOYSA-N 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
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150000003983 crown ethers Chemical class 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000001035 drying Methods 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
230000012173 estrus Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003502 gasoline Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000005457 ice water Substances 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
239000003595 mist Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000011368 organic material Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000006072 paste Substances 0.000 description 1
UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000002728 pyrethroid Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000012958 reprocessing Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000779 smoke Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000007704 transition Effects 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/743—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of acids with a three-membered ring and with unsaturation outside the 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
- 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
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
- C07C321/24—Thiols, sulfides, hydropolysulfides, or polysulfides having thio groups bound to carbon atoms of six-membered aromatic rings
- C07C321/28—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to carbon atoms of six-membered aromatic rings

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)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

DK176086A 1985-04-18 1986-04-17 Vinylcyclopropancarboxylsyreestre, deres fremstilling og anvendelse som plantebeskyttelsesmiddel, middel heraf og fremgangsmåde til fremstilling deraf og fremgangsmåde til bekæmpelse af skadelige organismer DK168287B1 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3513978		1985-04-18
DE19853513978 DE3513978A1 (de)	1985-04-18	1985-04-18	Vinylcyclopropancarbonsaeureester

Publications (3)

Publication Number	Publication Date
DK176086D0 DK176086D0 (da)	1986-04-17
DK176086A DK176086A (da)	1986-10-19
DK168287B1 true DK168287B1 (da)	1994-03-07

Family

ID=6268442

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK176086A DK168287B1 (da)	1985-04-18	1986-04-17	Vinylcyclopropancarboxylsyreestre, deres fremstilling og anvendelse som plantebeskyttelsesmiddel, middel heraf og fremgangsmåde til fremstilling deraf og fremgangsmåde til bekæmpelse af skadelige organismer

Country Status (29)

Country	Link
US (1)	US4820735A (hu)
EP (1)	EP0200943B1 (hu)
JP (2)	JPH0768189B2 (hu)
KR (1)	KR940010766B1 (hu)
CN (1)	CN1013861B (hu)
AR (1)	AR242782A1 (hu)
AT (1)	ATE39111T1 (hu)
AU (1)	AU592082B2 (hu)
BR (1)	BR8601715A (hu)
CA (1)	CA1280762C (hu)
CS (1)	CS258478B2 (hu)
DD (1)	DD244490A5 (hu)
DE (2)	DE3513978A1 (hu)
DK (1)	DK168287B1 (hu)
ES (1)	ES8704454A1 (hu)
FI (1)	FI87351C (hu)
GR (1)	GR861006B (hu)
HU (1)	HU203866B (hu)
IE (1)	IE58670B1 (hu)
IL (1)	IL78500A (hu)
MA (1)	MA20666A1 (hu)
NO (1)	NO163326C (hu)
NZ (1)	NZ215826A (hu)
PH (1)	PH22037A (hu)
PL (1)	PL148195B1 (hu)
PT (1)	PT82352B (hu)
TR (1)	TR24983A (hu)
ZA (1)	ZA862879B (hu)
ZW (1)	ZW6786A1 (hu)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2587589B1 (fr) *	1985-09-23	1990-05-11	Roussel Uclaf	Nouvelles compositions pesticides renfermant du (1r cis,e) 2,2-dimethyl 3/2-fluoro 3-oxo 3-methoxy 1-propenyl/cyclopropane carboxylate de pentafluoro phenyl methyl
GB8607920D0 (en) *	1986-04-01	1986-05-08	Cpc International Inc	Dry food composition
DE3705224A1 (de) *	1987-02-19	1988-09-01	Bayer Ag	(+)1r-trans-2,2-dimethyl-3-(2,2-dichlorvinyl) -cyclopropancarbonsaeure-2,3,5,6- tetrafluorbenzylester
IT1226546B (it) *	1988-07-07	1991-01-24	Mini Ricerca Scient Tecnolog	Esteri dell'acido 2,2-dimetil- ciclopropancarbossilico
FR2678609B1 (fr) *	1991-07-04	1994-08-26	Roussel Uclaf	Nouveaux esters pyrethrinouides de l'alcool 4-amino 2,3,5,6-tetrafluorophenyl methylique, leur procede de preparation et leur application comme pesticides.
CN102070439B (zh) *	2011-01-13	2013-01-02	浙江大学	(±)-2,2-二甲基-3-乙烯基环丙烷羧酸的制备方法
CN108218696B (zh) *	2016-12-21	2021-03-26	江苏优嘉植物保护有限公司	一种联苯菊酯的生产工艺

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2819788A1 (de) *	1978-05-05	1979-11-08	Bayer Ag	Benzylester mit fluorsubstituierten aether- und/oder thioaethergruppen und ihre verwendung als insektizide
DE2831193A1 (de) *	1978-07-15	1980-01-24	Bayer Ag	Fluoralkenylsubstituierte cyclopropancarbonsaeureester und ihre verwendung als insektizide
GB2066810A (en) *	1979-12-21	1981-07-15	Ici Ltd	Fluorinated benzyl esters of cyclopropane carboxylic acids
BR8008346A (pt) *	1979-12-21	1981-07-07	Ici Ltd	Compostos e composicoes inseticidas a base dos mesmos,bem como processo de sua obtencao
US4370346A (en) *	1979-12-21	1983-01-25	Imperial Chemical Industries Plc	Halogenated esters
DE3170890D1 (en) *	1980-12-17	1985-07-11	Ici Plc	Fluorobenzyl cyclopropane carboxylates, their preparation, compositions comprising them and their use as insecticides
GB2097384A (en) *	1981-03-18	1982-11-03	Ici Plc	Fluorinated benzyl esters of tetramethylcyclopropane carboxylic acid

1985
- 1985-04-18 DE DE19853513978 patent/DE3513978A1/de not_active Withdrawn
1986
- 1986-03-21 ZW ZW67/86A patent/ZW6786A1/xx unknown
- 1986-04-02 AR AR86303549A patent/AR242782A1/es active
- 1986-04-07 PH PH33626A patent/PH22037A/en unknown
- 1986-04-08 NO NO861365A patent/NO163326C/no unknown
- 1986-04-09 PT PT82352A patent/PT82352B/pt not_active IP Right Cessation
- 1986-04-09 DE DE8686104876T patent/DE3661357D1/de not_active Expired
- 1986-04-09 AT AT86104876T patent/ATE39111T1/de not_active IP Right Cessation
- 1986-04-09 EP EP86104876A patent/EP0200943B1/de not_active Expired
- 1986-04-10 CN CN86102323A patent/CN1013861B/zh not_active Expired
- 1986-04-15 TR TR86/0192A patent/TR24983A/xx unknown
- 1986-04-15 CS CS862758A patent/CS258478B2/cs unknown
- 1986-04-15 NZ NZ215826A patent/NZ215826A/xx unknown
- 1986-04-15 IL IL78500A patent/IL78500A/xx not_active IP Right Cessation
- 1986-04-16 GR GR861006A patent/GR861006B/el unknown
- 1986-04-16 DD DD86289241A patent/DD244490A5/de not_active IP Right Cessation
- 1986-04-16 MA MA20891A patent/MA20666A1/fr unknown
- 1986-04-16 FI FI861606A patent/FI87351C/fi not_active IP Right Cessation
- 1986-04-16 CA CA000506773A patent/CA1280762C/en not_active Expired - Lifetime
- 1986-04-17 HU HU861605A patent/HU203866B/hu not_active IP Right Cessation
- 1986-04-17 IE IE101786A patent/IE58670B1/en not_active IP Right Cessation
- 1986-04-17 AU AU56341/86A patent/AU592082B2/en not_active Ceased
- 1986-04-17 DK DK176086A patent/DK168287B1/da active
- 1986-04-17 PL PL1986259008A patent/PL148195B1/pl unknown
- 1986-04-17 BR BR8601715A patent/BR8601715A/pt not_active IP Right Cessation
- 1986-04-17 ES ES554092A patent/ES8704454A1/es not_active Expired
- 1986-04-17 JP JP61087231A patent/JPH0768189B2/ja not_active Expired - Lifetime
- 1986-04-17 ZA ZA862879A patent/ZA862879B/xx unknown
- 1986-04-18 KR KR1019860003005A patent/KR940010766B1/ko not_active Expired - Lifetime
1987
- 1987-08-18 US US07/087,999 patent/US4820735A/en not_active Expired - Fee Related
1993
- 1993-03-17 JP JP5081154A patent/JPH0749415B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
CA1280762C (en)	1991-02-26
FI861606L (fi)	1986-10-19
US4820735A (en)	1989-04-11
KR860008117A (ko)	1986-11-12
JPH0749415B2 (ja)	1995-05-31
CN1013861B (zh)	1991-09-11
PT82352B (pt)	1988-10-14
EP0200943B1 (de)	1988-12-07
NO163326B (no)	1990-01-29
ATE39111T1 (de)	1988-12-15
NZ215826A (en)	1989-03-29
FI87351B (fi)	1992-09-15
ES554092A0 (es)	1987-04-01
DE3513978A1 (de)	1986-10-30
BR8601715A (pt)	1986-12-16
MA20666A1 (fr)	1986-12-31
DD244490A5 (de)	1987-04-08
JPS61243049A (ja)	1986-10-29
IL78500A0 (en)	1986-08-31
AU592082B2 (en)	1990-01-04
PT82352A (en)	1986-05-01
IE861017L (en)	1986-10-18
FI87351C (fi)	1992-12-28
NO163326C (no)	1990-05-09
IL78500A (en)	1991-06-10
CS258478B2 (en)	1988-08-16
CS275886A2 (en)	1987-05-14
EP0200943A1 (de)	1986-11-12
ZA862879B (en)	1986-12-30
HUT41963A (en)	1987-06-29
ES8704454A1 (es)	1987-04-01
JPH0768189B2 (ja)	1995-07-26
PH22037A (en)	1988-05-13
CN86102323A (zh)	1986-12-03
DK176086A (da)	1986-10-19
PL148195B1 (en)	1989-09-30
DK176086D0 (da)	1986-04-17
GR861006B (en)	1986-08-12
IE58670B1 (en)	1993-11-03
FI861606A0 (fi)	1986-04-16
DE3661357D1 (de)	1989-01-12
KR940010766B1 (ko)	1994-11-11
NO861365L (no)	1986-10-20
ZW6786A1 (en)	1986-06-25
AU5634186A (en)	1986-10-23
JPH0649001A (ja)	1994-02-22
HU203866B (en)	1991-10-28
AR242782A1 (es)	1993-05-31
TR24983A (tr)	1992-08-17

Publication	Publication Date	Title
JPS6218538B2 (hu)	1987-04-23
JPS6312041B2 (hu)	1988-03-17
HU178441B (en)	1982-05-28	Insecticide and acaricide compositions containing fluoro-substituted phenoxy-bracket-banzyl-oxy-bracket closed-carbonyl-compounds and process for producing these materials
HU196604B (en)	1988-12-28	Insecticides, acaricides and nematocides comprising thionophosphoric acid ester derivatives as active ingredient and process for producing thionophosphoric acid esters applied as active ingredient
US4423066A (en)	1983-12-27	Combating arthropods with perfluorobenzyl 2,2-dimethyl-3-vinyl-cyclopropane carboxylates
DK168287B1 (da)	1994-03-07	Vinylcyclopropancarboxylsyreestre, deres fremstilling og anvendelse som plantebeskyttelsesmiddel, middel heraf og fremgangsmåde til fremstilling deraf og fremgangsmåde til bekæmpelse af skadelige organismer
US4376786A (en)	1983-03-15	Combating arthropods with 4-fluoro-3-phenoxy-benzyl 3-alken-1-yl-2,2-dimethyl-cyclopropanecarboxylates
US4699922A (en)	1987-10-13	Tetramethylcyclopropanecarboxylates
KR100420159B1 (ko)	2004-05-31	5,6-디하이드로-1,3-옥사진의제조방법
KR100346161B1 (ko)	2002-11-30	3-아릴-4-하이드록시-△3-디하이드로푸라논유도체
HU185236B (en)	1984-12-28	Pesticide compositions containing substituted esters of 3-bracket-1,2-dibromo-alkyl-bracket closed-2,2-dimethyl-cyclopropane-carboxylic acid and process for producing these compounds
DK161511B (da)	1991-07-15	Fluor-substituerede 2,2,3,3-tetramethyl-cyclopropan-1-carboxylsyre-benzylestere, fremgangsmaade til fremstilling deraf samt insekticide og acaricide midler indeholdende disse forbindelser
CS217991B2 (en)	1983-02-25	Insecticide and acaricide means and method of making the active agent
CS208123B2 (en)	1981-08-31	Insecticide and acaricide means and method of making the active substances
HU184682B (en)	1984-09-28	Insecticide and acaricide compositions containing phenoxy-benzyl-esters of substituted bromo-styryl-cyclopropane-carboxylic acid and process for preparing the active substances
CS220342B2 (en)	1983-03-25	Insecticide and acaricide composition and method of producing active component thereof
JPS6341381B2 (hu)	1988-08-17
KR860000558B1 (ko)	1986-05-14	2,2-디메틸-3-(2,2-디클로로비닐)-사이클로프로판-1-카복실산 α-시아노-3-페녹시-4-플루오로-벤질 에스테르의 입체 이성체의 제조방법
DE2837524A1 (de)	1980-03-20	Substituierte alpha-phenyl-carbonsaeure- (4-fluoro-3-phenoxy-benzyl)-ester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
DK160878B (da)	1991-04-29	O-alkyl-o-(3,5,6-trichlor-pyrid-2-yl)-alkylthionophosphonsyreestere, fremg. til deres fremst., middel til bekaempelse af skadelige organismer indeholdende forbindelserne, anvendelse af forbindelserne til bekaempelse af skadelige organismer, fremg. til bekaempelse af skadelige organismer under anvendelse af forb. og fremg. til fremst. af midler til bekaempelse af skade. organismer indeh. forbindelserne