DD145994A5 - Insektizide und/oder fungizide mittel - Google Patents

Insektizide und/oder fungizide mittel Download PDF

Info

Publication number: DD145994A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; iso; dimethyl; formula; chj
Prior art date: 1978-09-02

Application number

DD79215237A

Other languages

German (de)

English (en)

Inventor

Fritz Maurer

Rolf Schroeder

Ingeborg Hammann

Bernhard Homeyer

Paul-Ernst Frohberger

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.)

1978-09-02

Filing date

1979-08-28

Publication date

1981-01-21

1979-08-28 Application filed by Bayer Ag filed Critical Bayer Ag

1981-01-21 Publication of DD145994A5 publication Critical patent/DD145994A5/de

Links

239000000417 fungicide Substances 0.000 title abstract description 3
239000002917 insecticide Substances 0.000 title abstract description 3
125000000217 alkyl group Chemical group 0.000 claims abstract description 15
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
239000001257 hydrogen Substances 0.000 claims abstract description 10
230000000749 insecticidal effect Effects 0.000 claims abstract description 9
229910052736 halogen Inorganic materials 0.000 claims abstract description 3
150000002367 halogens Chemical class 0.000 claims abstract description 3
238000000034 method Methods 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 19
238000002360 preparation method Methods 0.000 claims description 16
239000003085 diluting agent Substances 0.000 claims description 15
241000238631 Hexapoda Species 0.000 claims description 6
230000000855 fungicidal effect Effects 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 4
239000004606 Fillers/Extenders Substances 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
241000233866 Fungi Species 0.000 claims 3
230000003032 phytopathogenic effect Effects 0.000 claims 3
230000001069 nematicidal effect Effects 0.000 claims 1
239000004480 active ingredient Substances 0.000 abstract description 8
239000000575 pesticide Substances 0.000 abstract description 6
150000002431 hydrogen Chemical class 0.000 abstract description 4
239000000463 material Substances 0.000 abstract description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
241000607479 Yersinia pestis Species 0.000 abstract description 2
239000003795 chemical substances by application Substances 0.000 abstract description 2
BPCFBUOIUJCLTD-UHFFFAOYSA-N pyrimidin-2-yl N,N-dimethoxycarbamate Chemical class CON(C(OC1=NC=CC=N1)=O)OC BPCFBUOIUJCLTD-UHFFFAOYSA-N 0.000 abstract description 2
101100242909 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) pbpA gene Proteins 0.000 abstract 2
101100269618 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) aliA gene Proteins 0.000 abstract 2
-1 for example Substances 0.000 description 74
KWCYOXGCAIGIGW-UHFFFAOYSA-N 4-methyl-2-(methylsulfanylmethyl)-5-propan-2-ylpyrimidine Chemical compound CSCC1=NC(=C(C=N1)C(C)C)C KWCYOXGCAIGIGW-UHFFFAOYSA-N 0.000 description 29
150000001875 compounds Chemical class 0.000 description 25
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
229910052757 nitrogen Inorganic materials 0.000 description 16
239000002904 solvent Substances 0.000 description 16
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 12
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
239000002253 acid Substances 0.000 description 10
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
238000009472 formulation Methods 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
125000004432 carbon atom Chemical group C* 0.000 description 8
239000003995 emulsifying agent Substances 0.000 description 8
238000002844 melting Methods 0.000 description 8
230000008018 melting Effects 0.000 description 8
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241000196324 Embryophyta Species 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000007858 starting material Substances 0.000 description 6
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical group CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
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239000000460 chlorine Substances 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
229910000027 potassium carbonate Inorganic materials 0.000 description 5
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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 4
206010061217 Infestation Diseases 0.000 description 4
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 4
229960000583 acetic acid Drugs 0.000 description 4
125000002877 alkyl aryl group Chemical group 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000000706 filtrate Substances 0.000 description 4
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230000009885 systemic effect Effects 0.000 description 4
150000008081 1H-pyrimidin-4-ones Chemical class 0.000 description 3
LNJMHEJAYSYZKK-UHFFFAOYSA-N 2-methylpyrimidine Chemical compound CC1=NC=CC=N1 LNJMHEJAYSYZKK-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
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GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052794 bromium Inorganic materials 0.000 description 3
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239000012141 concentrate Substances 0.000 description 3
238000001816 cooling Methods 0.000 description 3
239000013078 crystal Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
238000001914 filtration Methods 0.000 description 3
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000007800 oxidant agent Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000000725 suspension Substances 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
DNCYBUMDUBHIJZ-UHFFFAOYSA-N 1h-pyrimidin-6-one Chemical compound O=C1C=CN=CN1 DNCYBUMDUBHIJZ-UHFFFAOYSA-N 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
CJHNMYLMNBCRRB-UHFFFAOYSA-N 4,5-dimethyl-2-(methylsulfanylmethyl)pyrimidine Chemical compound CSCC1=NC(=C(C=N1)C)C CJHNMYLMNBCRRB-UHFFFAOYSA-N 0.000 description 2
GGHIZNIYMPVZHC-UHFFFAOYSA-N 5-ethyl-2-(propylsulfanylmethyl)pyrimidine Chemical compound C(CC)SCC1=NC=C(C=N1)CC GGHIZNIYMPVZHC-UHFFFAOYSA-N 0.000 description 2
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235000011303 Brassica alboglabra Nutrition 0.000 description 2
235000011302 Brassica oleracea Nutrition 0.000 description 2
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
YIIMEMSDCNDGTB-UHFFFAOYSA-N Dimethylcarbamoyl chloride Chemical compound CN(C)C(Cl)=O YIIMEMSDCNDGTB-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
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UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
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241000721623 Myzus Species 0.000 description 2
241000721621 Myzus persicae Species 0.000 description 2
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CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
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WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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125000001931 aliphatic group Chemical group 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
238000012512 characterization method Methods 0.000 description 2
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235000011152 sodium sulphate Nutrition 0.000 description 2
239000000126 substance Substances 0.000 description 2
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RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
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HILGSIWGSAQZMS-UHFFFAOYSA-N 2-(ethylsulfanylmethyl)pyrimidine Chemical compound CCSCc1ncccn1 HILGSIWGSAQZMS-UHFFFAOYSA-N 0.000 description 1
VLHGBZJHFWEHFY-UHFFFAOYSA-N 2-(ethylsulfonylmethyl)-5,6-dimethyl-1h-pyrimidin-4-one Chemical compound CCS(=O)(=O)CC1=NC(C)=C(C)C(O)=N1 VLHGBZJHFWEHFY-UHFFFAOYSA-N 0.000 description 1
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ZTFRXSJZFVDAKN-UHFFFAOYSA-N 4,5-dimethyl-2-(methylsulfinylmethyl)pyrimidine Chemical compound CS(=O)CC1=NC(=C(C=N1)C)C ZTFRXSJZFVDAKN-UHFFFAOYSA-N 0.000 description 1
HATROGJCGJWAJF-UHFFFAOYSA-N 4,5-dimethyl-2-(methylsulfonylmethyl)pyrimidine Chemical compound CS(=O)(=O)CC1=NC(=C(C=N1)C)C HATROGJCGJWAJF-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
- C07D239/90—Oxygen atoms with acyclic radicals attached in position 2 or 3
- 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems

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)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DD79215237A 1978-09-02 1979-08-28 Insektizide und/oder fungizide mittel DD145994A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782838359 DE2838359A1 (de)	1978-09-02	1978-09-02	N,n-dimethyl-0-pyrimidinyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel

Publications (1)

Publication Number	Publication Date
DD145994A5 true DD145994A5 (de)	1981-01-21

Family

ID=6048552

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79215237A DD145994A5 (de)	1978-09-02	1979-08-28	Insektizide und/oder fungizide mittel

Country Status (13)

Country	Link
US (1)	US4234587A (da)
EP (1)	EP0008762B1 (da)
JP (1)	JPS5535088A (da)
AU (1)	AU5047079A (da)
BR (1)	BR7905611A (da)
DD (1)	DD145994A5 (da)
DE (2)	DE2838359A1 (da)
DK (1)	DK366279A (da)
ES (1)	ES483785A1 (da)
IL (1)	IL58148A (da)
PL (1)	PL218080A1 (da)
PT (1)	PT70124A (da)
ZA (1)	ZA794623B (da)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2928185A1 (de) *	1979-07-12	1981-01-29	Bayer Ag	N,n-dimethyl-o-pyrimidinyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
US4343803A (en) *	1981-05-04	1982-08-10	Olin Corporation	2-Trichloromethyl-4-pyrimidinyl carbamates and their use as fungicides
US4395551A (en) *	1981-12-10	1983-07-26	Uniroyal, Inc.	Pyridopyrimidinone compounds
DE3211035A1 (de) *	1982-03-25	1983-09-29	Bayer Ag, 5090 Leverkusen	Substituierte n,n-dimethyl-o-pyrimidin-e-yl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
EP0100795A1 (en) *	1982-08-06	1984-02-22	Olin Corporation	Selected 2-trichloromethyl-4-pyrimidinyl carbamates and their use as fungicides
EP0218171A3 (de) *	1985-10-09	1988-01-13	Bayer Ag	Verfahren zur Herstellung von 2-Alkylsulfonylalkylen-pyrimidinen
US4786640A (en) *	1987-06-12	1988-11-22	American Home Products Corporation	2,6-disubstituted-5-cyano-4-pyrimidinyloxyacetic acid aldose reductase inhibitors
DE3911488A1 (de) *	1989-04-08	1990-10-11	Bayer Ag	Pyrimidin-4-yl-carbamidsaeureester

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA519436A (en) *	1949-08-22	1955-12-13	Gysin Hans	Carbamic acid esters as well as pest combatting agents and a method of making the same
FR1060289A (fr) *	1951-07-16	1954-03-31	Geigy Ag J R	Dérivés hétérocycliques de l'acide carbamique et leur procédé de préparation
GB1263260A (en) *	1968-10-29	1972-02-09	Ici Ltd	Pyrimidine derivatives and compositions containing them
DE2752613A1 (de) *	1977-11-25	1979-06-07	Bayer Ag	N,n-dialkyl-0-pyrimidinyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide

1978
- 1978-09-02 DE DE19782838359 patent/DE2838359A1/de not_active Withdrawn
1979
- 1979-08-22 US US06/068,795 patent/US4234587A/en not_active Expired - Lifetime
- 1979-08-27 PT PT70124A patent/PT70124A/pt unknown
- 1979-08-27 EP EP79103155A patent/EP0008762B1/de not_active Expired
- 1979-08-27 DE DE7979103155T patent/DE2961070D1/de not_active Expired
- 1979-08-28 DD DD79215237A patent/DD145994A5/de unknown
- 1979-08-30 IL IL58148A patent/IL58148A/xx unknown
- 1979-08-31 ES ES483785A patent/ES483785A1/es not_active Expired
- 1979-08-31 AU AU50470/79A patent/AU5047079A/en not_active Abandoned
- 1979-08-31 ZA ZA00794623A patent/ZA794623B/xx unknown
- 1979-08-31 JP JP11053579A patent/JPS5535088A/ja active Pending
- 1979-08-31 BR BR7905611A patent/BR7905611A/pt unknown
- 1979-08-31 DK DK366279A patent/DK366279A/da not_active Application Discontinuation
- 1979-09-01 PL PL21808079A patent/PL218080A1/xx unknown

Also Published As

Publication number	Publication date
DE2838359A1 (de)	1980-03-20
IL58148A0 (en)	1979-12-30
IL58148A (en)	1983-09-30
ZA794623B (en)	1980-09-24
EP0008762B1 (de)	1981-10-21
BR7905611A (pt)	1980-05-13
JPS5535088A (en)	1980-03-11
AU5047079A (en)	1980-03-13
EP0008762A1 (de)	1980-03-19
DK366279A (da)	1980-03-03
PT70124A (en)	1979-09-01
PL218080A1 (da)	1980-06-16
US4234587A (en)	1980-11-18
DE2961070D1 (en)	1981-12-24
ES483785A1 (es)	1980-05-16

Publication	Publication Date	Title
EP0315826A1 (de)	1989-05-17	Imidazoline
EP0009634A1 (de)	1980-04-16	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0008762B1 (de)	1981-10-21	N,N-Dimethyl-O-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0017066B1 (de)	1982-04-28	N,N-Dimethyl-O-pyrazolyl-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
DE2644588C2 (de)	1987-02-19	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0043978B1 (de)	1983-08-24	N-Phosphonylcarbonyl-Carbamate, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Schädlingsbekämpfungsmittel und ihre Verwendung zur Schädlingsbekämpfung
EP0002200B1 (de)	1981-09-02	N,N-Dialkyl-O-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0005240B1 (de)	1981-04-29	N,N-Dimethyl-O-pyrazolyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0000198B1 (de)	1980-07-23	N,N-Dialkyl-0-pyrimidinyl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
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
EP0062821B1 (de)	1985-05-22	N-Alkyl-O-pyrazol-4-yl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0069881A1 (de)	1983-01-19	S-Azolyl-methyl-di(tri)-thiophosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0090247B1 (de)	1986-07-23	Substituierte N,N-Dimethyl-O-pyrimidin-4-yl-carbamin-säureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0168704B1 (de)	1988-06-22	Pyrimidinyl-thionophosphorsäureester
EP0087561B1 (de)	1986-01-29	N,N-Dimethyl-0-(1-carbamoyl-5-pyrazolyl)-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0392240B1 (de)	1994-05-11	Pyrimidin-4-yl-carbamidsäureester
DE3438919A1 (de)	1986-04-24	Substituierte phenyl-carbaminsaeureester
DE2732101A1 (de)	1979-01-25	Pyridazinon(thiono)-phosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0000895A1 (de)	1979-03-07	Aryl-N-alkyl-carbamate, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0075144A1 (de)	1983-03-30	N,N-Dimethyl-O-imidazol-4-yl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel