DD256638A5 - Insektizide, akarizide, nematozide und molluskizide mittel - Google Patents

Insektizide, akarizide, nematozide und molluskizide mittel Download PDF

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Publication number: DD256638A5
Authority: DD; German Democratic Republic
Prior art keywords: ocf; alkyl; halogenated; halogen; chfcf
Prior art date: 1985-12-21

Application number

DD86297904A

Other languages

German (de)

English (en)

Inventor

Volker Koch

Andreas Fuss

Werner Bonin

Werner Knauf

Anna Waltersdorfer

Original Assignee

��@��k��

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.)

1985-12-21

Filing date

1986-12-18

Publication date

1988-05-18

1986-12-18 Application filed by ��@��k�� filed Critical ��@��k��

1988-05-18 Publication of DD256638A5 publication Critical patent/DD256638A5/de

Links

239000002917 insecticide Substances 0.000 title description 3
239000000642 acaricide Substances 0.000 title description 2
239000005645 nematicide Substances 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 81
239000004480 active ingredient Substances 0.000 claims abstract description 18
239000000203 mixture Substances 0.000 claims abstract description 17
241000238631 Hexapoda Species 0.000 claims abstract description 10
241000244206 Nematoda Species 0.000 claims abstract description 5
230000000895 acaricidal effect Effects 0.000 claims abstract description 5
241000237852 Mollusca Species 0.000 claims abstract description 4
230000000749 insecticidal effect Effects 0.000 claims abstract description 4
230000002013 molluscicidal effect Effects 0.000 claims abstract description 4
230000001069 nematicidal effect Effects 0.000 claims abstract description 4
229910052736 halogen Inorganic materials 0.000 claims description 30
150000002367 halogens Chemical group 0.000 claims description 30
-1 phenylsulfenyl Chemical group 0.000 claims description 30
238000000034 method Methods 0.000 claims description 21
150000003254 radicals Chemical class 0.000 claims description 17
125000000217 alkyl group Chemical group 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 7
125000004093 cyano group Chemical group *C#N 0.000 claims description 7
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 6
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 6
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
229910052760 oxygen Inorganic materials 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 4
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 4
KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical compound O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
239000000969 carrier Substances 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
125000001425 triazolyl group Chemical group 0.000 claims description 3
125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 2
125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 2
125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000002883 imidazolyl group Chemical group 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 2
125000001863 phosphorothioyl group Chemical group *P(*)(*)=S 0.000 claims description 2
125000003226 pyrazolyl group Chemical group 0.000 claims description 2
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 1
230000001473 noxious effect Effects 0.000 claims 1
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 1
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NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
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ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 2
ZRJSABISRHPRSB-UHFFFAOYSA-N 2,6-difluorobenzoyl isocyanate Chemical compound FC1=CC=CC(F)=C1C(=O)N=C=O ZRJSABISRHPRSB-UHFFFAOYSA-N 0.000 description 2
NZXURVQEEZUDOT-UHFFFAOYSA-N 3-chloro-2-(2,6-dichloro-4-isocyanatophenoxy)-5-(difluoromethoxy)pyridine Chemical compound ClC1=CC(OC(F)F)=CN=C1OC1=C(Cl)C=C(N=C=O)C=C1Cl NZXURVQEEZUDOT-UHFFFAOYSA-N 0.000 description 2
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LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
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CGTWCAVZZBLHQH-UHFFFAOYSA-N [cyano-(3-phenoxyphenyl)methyl] 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropane-1-carboxylate Chemical compound C1=CC(OCC)=CC=C1C1(C(=O)OC(C#N)C=2C=C(OC=3C=CC=CC=3)C=CC=2)C(Cl)(Cl)C1 CGTWCAVZZBLHQH-UHFFFAOYSA-N 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
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238000009835 boiling Methods 0.000 description 2
150000004657 carbamic acid derivatives Chemical class 0.000 description 2
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DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 2
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VZPRFNYMFQEGNV-UHFFFAOYSA-N naphthalen-2-ylmethyl cyclopropanecarboxylate Chemical compound C=1C=C2C=CC=CC2=CC=1COC(=O)C1CC1 VZPRFNYMFQEGNV-UHFFFAOYSA-N 0.000 description 2
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DXEMHWAAAJAXBG-UHFFFAOYSA-N (3-methyl-5-propan-2-ylphenyl) n-butanoyl-n-methylcarbamate Chemical compound CCCC(=O)N(C)C(=O)OC1=CC(C)=CC(C(C)C)=C1 DXEMHWAAAJAXBG-UHFFFAOYSA-N 0.000 description 1
125000006702 (C1-C18) alkyl group Chemical group 0.000 description 1
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XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 description 1
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CZZZABOKJQXEBO-UHFFFAOYSA-N 2,4-dimethylaniline Chemical class CC1=CC=C(N)C(C)=C1 CZZZABOKJQXEBO-UHFFFAOYSA-N 0.000 description 1
RELFZPZYUIBSFE-UHFFFAOYSA-N 2-(nitromethyl)-1,3-thiazolidine Chemical compound [O-][N+](=O)CC1NCCS1 RELFZPZYUIBSFE-UHFFFAOYSA-N 0.000 description 1
OWMUJGVUSWFZKG-UHFFFAOYSA-N 2-(nitromethyl)thiazinane Chemical compound [O-][N+](=O)CN1CCCCS1 OWMUJGVUSWFZKG-UHFFFAOYSA-N 0.000 description 1
CMJUNAQINNWKAU-KTKRTIGZSA-N 2-[[(z)-2-oxononadec-10-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)CNCCS(O)(=O)=O CMJUNAQINNWKAU-KTKRTIGZSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/69—Two or more oxygen atoms
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Pyridine Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DD86297904A 1985-12-21 1986-12-18 Insektizide, akarizide, nematozide und molluskizide mittel DD256638A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19853545569 DE3545569A1 (de)	1985-12-21	1985-12-21	Neue pyridin-derivate, verfahren zu ihrer herstellung, sie enthaltene mittel und ihre verwendung als schaedlingsbekaempfungsmittel

Publications (1)

Publication Number	Publication Date
DD256638A5 true DD256638A5 (de)	1988-05-18

Family

ID=6289243

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86297904A DD256638A5 (de)	1985-12-21	1986-12-18	Insektizide, akarizide, nematozide und molluskizide mittel

Country Status (14)

Country	Link
US (1)	US4855309A (fr)
EP (1)	EP0227046A3 (fr)
JP (1)	JPS62164666A (fr)
CN (1)	CN86108620A (fr)
AU (1)	AU588409B2 (fr)
BR (1)	BR8606340A (fr)
DD (1)	DD256638A5 (fr)
DE (1)	DE3545569A1 (fr)
DK (1)	DK618986A (fr)
HU (1)	HUT43924A (fr)
IL (1)	IL81044A0 (fr)
OA (1)	OA08449A (fr)
PT (1)	PT83994B (fr)
ZA (1)	ZA869559B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3545571A1 (de) *	1985-12-21	1987-06-25	Hoechst Ag	Heterocyclische phenylaether, verfahren zu deren herstellung und diese enthaltende herbizide mittel
ZA903739B (en) *	1989-05-27	1991-03-27	Sumitomo Chemical Co	A poison bait for control of noxious insects
WO1997009882A1 (fr) *	1995-09-14	1997-03-20	Valent U.S.A. Corporation	Sable enduit de phosphoroamidothioate et procede correspondant
US6806367B2 (en) *	2001-10-26	2004-10-19	Ishihara Sangyo Kaisha, Ltd.	Process for producing carbonyl hydrazones
SG11201509186TA (en)	2013-06-27	2016-01-28	Pfizer	Heteroaromatic compounds and their use as dopamine d1 ligands

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3931201A (en) *	1974-01-22	1976-01-06	The Dow Chemical Company	Substituted pyridinyloxy(thio)phenyl -acetamides, -ureas and urea derivatives
JPS5823871B2 (ja) *	1978-02-06	1983-05-18	石原産業株式会社	Ｎ↓−ピリジルオキシフエニルウレア系化合物及びそれらを含有する殺虫剤
AU532156B2 (en) *	1979-09-07	1983-09-22	Ishihara Sangyo Kaisha Ltd.	N-benzoyl-n'-pyridyloxy phenyl urea
DE3240975A1 (de) *	1981-11-09	1983-05-19	CIBA-GEIGY AG, 4002 Basel	Phenylbenzoylharnstoffe und -thioharnstoffe
DE3275720D1 (de) *	1981-11-10	1987-04-23	Ciba Geigy Ag	Phenylbenzoyl ureas as pesticides
EP0101662A3 (fr) *	1982-06-25	1985-12-04	Ciba-Geigy Ag	Acides benzoylparabanoiques
EP0109211A1 (fr) *	1982-11-05	1984-05-23	Imperial Chemical Industries Plc	Dérivés de la pyridine
CA1233822A (fr) *	1982-12-30	1988-03-08	David T. Chou	Benzoyl urees pesticides et procede de preparation
US4550108A (en) *	1983-08-17	1985-10-29	Ciba Geigy Corporation	1,3,5-Oxadiazine-2,4-diones and pesticidal use
US4723015A (en) *	1983-10-17	1988-02-02	Ciba-Geigy Corporation	Certain insecticidal N-2-pyridyloxyphenylbenzimidates
ATE40111T1 (de) *	1984-07-05	1989-02-15	Duphar Int Res	Benzoylharnstoffverbindungen sowie solche enthaltende insektizide und akarizide zusammensetzungen.
AU601145B2 (en) *	1985-03-01	1990-09-06	Duphar International Research B.V.	Benzoyl urea derivatives having anti-tumor activity

1985
- 1985-12-21 DE DE19853545569 patent/DE3545569A1/de not_active Withdrawn
1986
- 1986-12-18 EP EP86117656A patent/EP0227046A3/fr not_active Withdrawn
- 1986-12-18 DD DD86297904A patent/DD256638A5/de not_active IP Right Cessation
- 1986-12-18 OA OA59020A patent/OA08449A/fr unknown
- 1986-12-19 IL IL81044A patent/IL81044A0/xx unknown
- 1986-12-19 AU AU66757/86A patent/AU588409B2/en not_active Ceased
- 1986-12-19 ZA ZA869559A patent/ZA869559B/xx unknown
- 1986-12-19 US US06/944,323 patent/US4855309A/en not_active Expired - Fee Related
- 1986-12-19 HU HU865353A patent/HUT43924A/hu unknown
- 1986-12-19 BR BR8606340A patent/BR8606340A/pt unknown
- 1986-12-19 DK DK618986A patent/DK618986A/da not_active Application Discontinuation
- 1986-12-20 CN CN198686108620A patent/CN86108620A/zh active Pending
- 1986-12-20 JP JP61302887A patent/JPS62164666A/ja active Pending
- 1986-12-22 PT PT83994A patent/PT83994B/pt not_active IP Right Cessation

Also Published As

Publication number	Publication date
PT83994A (de)	1987-01-01
ZA869559B (en)	1987-10-28
JPS62164666A (ja)	1987-07-21
HUT43924A (en)	1988-01-28
US4855309A (en)	1989-08-08
DK618986D0 (da)	1986-12-19
OA08449A (fr)	1988-06-30
PT83994B (pt)	1989-07-31
CN86108620A (zh)	1987-08-05
DE3545569A1 (de)	1987-06-25
EP0227046A3 (fr)	1988-09-21
DK618986A (da)	1987-06-22
IL81044A0 (en)	1987-03-31
AU6675786A (en)	1987-06-25
BR8606340A (pt)	1987-10-13
EP0227046A2 (fr)	1987-07-01
AU588409B2 (en)	1989-09-14

Legal Events

Date	Code	Title	Description
1994-12-08	PJ	Ceased due to non-payment of renewal fee (addendum to changes before extension act)

Publication	Publication Date	Title
DE4131924A1 (de)	1993-07-08	Substituierte 4-alkoxypyrimidine, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
DE4208254A1 (de)	1993-09-16	Substituierte pyrimidine, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel und fungizid
NZ221686A (en)	1990-04-26	Compounds containing two separate heterocyclic rings and insecticidal compositions
EP0093976A1 (fr)	1983-11-16	Urées et thiourées 2,4-dihalogenbenzoyles, procédés pour leur fabrication et leur utilisation comme pesticides
DE19518054A1 (de)	1996-09-12	N-Arylpyrazolketone und deren Derivate, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel
DE19858191A1 (de)	2000-06-21	4-Haloalkyl-3-heterocyclylpyridine und 4-Haloalkyl-5-heterocyclyl-pyrimidine und ihre Verwendung als Repellentien
DE19858192A1 (de)	2000-06-21	4-Trifluormethyl-3-oxazolylpyridine, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel
DE19858193A1 (de)	2000-06-21	4-Trifluormethyl-3-oxadiazolylpyridine, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel
DE4213149A1 (de)	1993-10-28	Akarizide, insektizide und nematizide substituierte (Hetero)-Aryl-Alkyl-ketonoxim-O-ether, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0135894B1 (fr)	1989-08-23	N-carbamoylarylcarboximidates, procédé de préparation, compositions et utilisation pesticide
DE4417163A1 (de)	1995-11-23	Heterocyclylamino- und Heterocyclyloxy-cycloalkyl-Derivate, ihre Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel und Fungizide
DE3644799A1 (de)	1987-12-10	Neue pyrimidin-derivate, deren herstellung und verwendung
DE3613062A1 (de)	1987-10-29	N-benzoyl-n'-phenyl(thio)harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
EP0248348A1 (fr)	1987-12-09	Pesticides à base de dérivés de l'aminopyrimidine ainsi que composés aminopyrimidiniques
US4855309A (en)	1989-08-08	Pyridine derivatives, agents containing same, and the use thereof as pesticides
DE3802175A1 (de)	1989-08-03	N-phenylbenzamide und n-phenylbenzamidoxime, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als schaedlingsbekaempfungsmittel
EP0318882B1 (fr)	1993-06-23	(Thio)benzoylurées, leurs dérivés fonctionnels, procédé de préparation, compositions et utilisation comme pesticide
DE3810379A1 (de)	1989-10-12	Azaneophyl- und silazaneophylsulfide, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als schaedlingsbekaempfungsmittel
DE4331180A1 (de)	1995-03-16	Substituierte Pyridine, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel und Fungizide
DE3903404A1 (de)	1990-08-09	Pyrimidintrionderivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als schaedlingsbekaempfungsmittel
EP0386715B1 (fr)	1995-02-15	Dérivés hétéroaryl-aryl-butène-et-butane, procédé pour leur préparation, compositions les contenant et leur utilisation comme biocides
MXPA97003150A (en)	1997-06-01	Derivatives of heterociclilamino and heterocicliloxi-cicloalquenilo and its use as control agents depests and fungici
EP0199945A2 (fr)	1986-11-05	Esters d'acides carbamoylarylcarboximides, leur procédé de préparation, compositions les contenant et leur utilisation comme pesticide
EP0311962A2 (fr)	1989-04-19	Phosphates de pyridyle, leur procédé de préparation, composition les contenant et son utilisation comme pesticide
DE4117076A1 (de)	1992-11-26	Substituierte 4-hetaryl-pyrazoline