DD143390A5 - Neue insektizide - Google Patents

Neue insektizide Download PDF

Info

Publication number: DD143390A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; formula; dimethyl; pyrazole; butyl
Prior art date: 1978-05-06

Application number

DD79212677A

Other languages

German (de)

English (en)

Inventor

Fritz Maurer

Hans-Jochem Riebel

Rolf Schroeder

Ingeborg Hammann

Bernhard Homeyer

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.)

1978-05-06

Filing date

1979-05-04

Publication date

1980-08-20

1979-05-04 Application filed by Bayer Ag filed Critical Bayer Ag

1980-08-20 Publication of DD143390A5 publication Critical patent/DD143390A5/de

Links

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WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
241001509970 Reticulitermes <genus> Species 0.000 description 1
241000125167 Rhopalosiphum padi Species 0.000 description 1
235000011034 Rubus glaucus Nutrition 0.000 description 1
244000235659 Rubus idaeus Species 0.000 description 1
235000009122 Rubus idaeus Nutrition 0.000 description 1
241000316887 Saissetia oleae Species 0.000 description 1
241000253973 Schistocerca gregaria Species 0.000 description 1
241001157779 Scutigera Species 0.000 description 1
241001313237 Scutigerella immaculata Species 0.000 description 1
239000004113 Sepiolite Substances 0.000 description 1
241000258242 Siphonaptera Species 0.000 description 1
241000180219 Sitobion avenae Species 0.000 description 1
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241000339374 Thrips tabaci Species 0.000 description 1
241001414989 Thysanoptera Species 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
241001238451 Tortrix viridana Species 0.000 description 1
241000018137 Trialeurodes vaporariorum Species 0.000 description 1
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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
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 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
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235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 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
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 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
150000001298 alcohols Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 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
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
125000000129 anionic group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000011230 binding agent Substances 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
229910052794 bromium Inorganic materials 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000002775 capsule Substances 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
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
239000004927 clay Substances 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
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000036576 dermal application Effects 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
229960001760 dimethyl sulfoxide Drugs 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000009189 diving Effects 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000008393 encapsulating agent Substances 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
230000012173 estrus Effects 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
235000013312 flour Nutrition 0.000 description 1
239000002816 fuel additive Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000002429 hydrazines Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
238000001802 infusion Methods 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex 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
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238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 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
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose 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
APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 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
230000007935 neutral effect Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 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
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229910052625 palygorskite Inorganic materials 0.000 description 1
239000003208 petroleum Substances 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
239000011148 porous material Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
239000004540 pour-on Substances 0.000 description 1
230000002035 prolonged effect Effects 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
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
238000001953 recrystallisation Methods 0.000 description 1
239000011435 rock Substances 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
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 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
241000894007 species Species 0.000 description 1
239000004544 spot-on Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 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
239000003039 volatile agent Substances 0.000 description 1
239000002023 wood 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/24—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms having sulfone or sulfonic acid radicals in the molecule
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5

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)
Plural Heterocyclic Compounds (AREA)

DD79212677A 1978-05-06 1979-05-04 Neue insektizide DD143390A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782819932 DE2819932A1 (de)	1978-05-06	1978-05-06	N,n-dimethyl-o-pyrazolyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide

Publications (1)

Publication Number	Publication Date
DD143390A5 true DD143390A5 (de)	1980-08-20

Family

ID=6038809

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79212677A DD143390A5 (de)	1978-05-06	1979-05-04	Neue insektizide

Country Status (14)

Country	Link
US (1)	US4215132A (pt)
EP (1)	EP0005240B1 (pt)
JP (1)	JPS54145663A (pt)
AT (1)	AT362620B (pt)
AU (1)	AU4668179A (pt)
BR (1)	BR7902731A (pt)
DD (1)	DD143390A5 (pt)
DE (2)	DE2819932A1 (pt)
DK (1)	DK185379A (pt)
ES (1)	ES480247A1 (pt)
IL (1)	IL57203A0 (pt)
PL (1)	PL215385A1 (pt)
PT (1)	PT69565A (pt)
ZA (1)	ZA792149B (pt)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2912494A1 (de) *	1979-03-29	1980-10-09	Bayer Ag	N,n-dimethyl-0-pyrazolyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
DE3202625A1 (de) *	1982-01-27	1983-08-04	Bayer Ag, 5090 Leverkusen	N,n-dimethyl-o-(1-carbamoyl-5-pyrazolyl)-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
DE3509567A1 (de) *	1985-03-16	1986-09-18	Bayer Ag, 5090 Leverkusen	Herbizide und insektizide mittel auf basis von pyrazolderivaten
DE3602728A1 (de) *	1985-05-17	1986-11-20	Bayer Ag, 51373 Leverkusen	Schaedlingsbekaempfungsmittel auf basis von pyrazolderivaten
DE3609423A1 (de) *	1986-03-20	1987-10-01	Bayer Ag	Schaedlingsbekaempfungsmittel auf basis von 1-aryl-4-trifluormethyl-5-aminopyrazolen

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH437904A (de) *	1964-03-13	1967-06-15	Agripat Sa	Schädlingsbekämpfungsmittel
DE2644589A1 (de) *	1976-10-02	1978-04-06	Bayer Ag	Tert.-butylsubstituierte pyrazolylcarbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und nematizide
DD133034A5 (de) *	1976-10-02	1978-11-29	Bayer Ag	Insektizide mittel
DE2644588C2 (de) *	1976-10-02	1987-02-19	Bayer Ag, 5090 Leverkusen	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide

1978
- 1978-05-06 DE DE19782819932 patent/DE2819932A1/de not_active Withdrawn
1979
- 1979-04-04 BR BR7902731A patent/BR7902731A/pt unknown
- 1979-04-18 US US06/031,096 patent/US4215132A/en not_active Expired - Lifetime
- 1979-04-26 DE DE7979101258T patent/DE2960299D1/de not_active Expired
- 1979-04-26 EP EP79101258A patent/EP0005240B1/de not_active Expired
- 1979-04-30 PT PT69565A patent/PT69565A/pt unknown
- 1979-05-03 IL IL57203A patent/IL57203A0/xx unknown
- 1979-05-04 AU AU46681/79A patent/AU4668179A/en not_active Abandoned
- 1979-05-04 AT AT334879A patent/AT362620B/de not_active IP Right Cessation
- 1979-05-04 DK DK185379A patent/DK185379A/da unknown
- 1979-05-04 DD DD79212677A patent/DD143390A5/de unknown
- 1979-05-04 ES ES480247A patent/ES480247A1/es not_active Expired
- 1979-05-04 JP JP5520279A patent/JPS54145663A/ja active Pending
- 1979-05-04 ZA ZA792149A patent/ZA792149B/xx unknown
- 1979-05-05 PL PL21538579A patent/PL215385A1/xx unknown

Also Published As

Publication number	Publication date
AU4668179A (en)	1979-11-08
BR7902731A (pt)	1979-11-20
PT69565A (en)	1979-05-01
EP0005240A3 (en)	1979-11-28
EP0005240A2 (de)	1979-11-14
JPS54145663A (en)	1979-11-14
DE2819932A1 (de)	1979-11-15
ES480247A1 (es)	1979-11-01
US4215132A (en)	1980-07-29
DE2960299D1 (en)	1981-08-06
ZA792149B (en)	1980-06-25
ATA334879A (de)	1980-10-15
EP0005240B1 (de)	1981-04-29
DK185379A (da)	1979-11-07
AT362620B (de)	1981-06-10
IL57203A0 (en)	1979-09-30
PL215385A1 (pt)	1980-06-16

Publication	Publication Date	Title
EP0315826A1 (de)	1989-05-17	Imidazoline
CH634304A5 (de)	1983-01-31	Phenylcarbamoyl-pyrazoline, verfahren zu deren herstellung sowie die verbindungen enthaltende insektizide.
EP0004022A1 (de)	1979-09-19	Pentafluorbenzyloxycarbonylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide
EP0316845B1 (de)	1994-01-19	1,2,3,4-Tetrahydro-5-nitro-pyrimidin-Derivate
EP0017066B1 (de)	1982-04-28	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0043978B1 (de)	1983-08-24	N-Phosphonylcarbonyl-Carbamate, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Schädlingsbekämpfungsmittel und ihre Verwendung zur Schädlingsbekämpfung
DE2644588C2 (de)	1987-02-19	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0008762B1 (de)	1981-10-21	N,N-Dimethyl-O-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0022511B1 (de)	1983-03-09	N,N-Dimethyl-O-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Schädlingsbekämpfungsmittel
EP0005240B1 (de)	1981-04-29	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
DE2644589A1 (de)	1978-04-06	Tert.-butylsubstituierte pyrazolylcarbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und nematizide
EP0000198B1 (de)	1980-07-23	N,N-Dialkyl-0-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
DE3739264A1 (de)	1989-06-01	2-chlor-1,3-thiazol-5-yl-methyl substituierte nitrogruppenhaltige imidazolidino-1,2,3,4-tetrahydropyrimidine bzw. hexahydropyrimidino-1,2,3,4-tetrahydropyrimidine
DE3012642A1 (de)	1981-10-08	3-carbamoyl-4-hydroxy-cumarine, verfahren zu ihrer herstellung als schaedlingsbekaepfungsmittel
EP0062821B1 (de)	1985-05-22	N-Alkyl-O-pyrazol-4-yl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0009103B1 (de)	1981-04-29	N-(O-Äthyl-S-n-propyl-(di)thiophosphoryloxy)-naphtalimide, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Schädlingsbekämpfungsmittel, ihre Herstellung und Verwendung
DE2831165A1 (de)	1980-01-24	2-cyclopropyl-pyrimidin(4)yl-thionophosphonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0090247B1 (de)	1986-07-23	Substituierte N,N-Dimethyl-O-pyrimidin-4-yl-carbamin-säureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
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