AP1004A - Pesticidal 1-aryl and pyridylpyrazole derivatives. - Google Patents

Pesticidal 1-aryl and pyridylpyrazole derivatives. Download PDF

Info

Publication number: AP1004A
Authority: AP; ARIPO
Prior art keywords: alkyl; formula; compound; amino; trifluoromethylphenyl
Prior art date: 1996-12-24

Application number

APAP/P/1999/001586A

Other languages

English (en)

Other versions

AP9901586A0 (en

Inventor

David Treadway Manning

Michael Thomas Pilato

Tei-The Wu

David William Hawkins

Original Assignee

Rhone Poulenc Agrochimie

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.)

1996-12-24

Filing date

1997-12-18

Publication date

2001-08-28

1997-12-18 Application filed by Rhone Poulenc Agrochimie filed Critical Rhone Poulenc Agrochimie

1999-06-30 Publication of AP9901586A0 publication Critical patent/AP9901586A0/xx

2001-08-28 Application granted granted Critical

2001-08-28 Publication of AP1004A publication Critical patent/AP1004A/en

Links

230000000361 pesticidal effect Effects 0.000 title claims abstract description 15
-1 hydroxy aminosulfonyl Chemical group 0.000 claims abstract description 87
125000000217 alkyl group Chemical group 0.000 claims abstract description 69
229910052736 halogen Inorganic materials 0.000 claims abstract description 27
150000002367 halogens Chemical class 0.000 claims abstract description 27
125000003342 alkenyl group Chemical group 0.000 claims abstract description 24
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 24
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 20
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 17
229910052731 fluorine Inorganic materials 0.000 claims abstract description 14
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 11
125000004457 alkyl amino carbonyl group Chemical group 0.000 claims abstract description 10
125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims abstract description 10
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 9
125000003545 alkoxy group Chemical group 0.000 claims abstract description 8
125000004691 alkyl thio carbonyl group Chemical group 0.000 claims abstract description 8
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 8
125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 8
125000000304 alkynyl group Chemical group 0.000 claims abstract description 7
125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims abstract description 6
125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
125000003435 aroyl group Chemical group 0.000 claims abstract description 4
239000001257 hydrogen Substances 0.000 claims abstract description 4
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 3
125000001475 halogen functional group Chemical group 0.000 claims abstract description 3
125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 145
239000000203 mixture Substances 0.000 claims description 85
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238000006243 chemical reaction Methods 0.000 claims description 24
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229910052801 chlorine Inorganic materials 0.000 claims description 19
229910052794 bromium Inorganic materials 0.000 claims description 18
150000003254 radicals Chemical class 0.000 claims description 13
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 8
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 8
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230000003647 oxidation Effects 0.000 claims description 6
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235000011152 sodium sulphate Nutrition 0.000 description 1
VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
MFSDELSXOVOZBJ-UHFFFAOYSA-M sodium;dodecyl sulfate;propane-1,2,3-triol Chemical compound [Na+].OCC(O)CO.CCCCCCCCCCCCOS([O-])(=O)=O MFSDELSXOVOZBJ-UHFFFAOYSA-M 0.000 description 1
ZNKXTIAQRUWLRL-UHFFFAOYSA-M sodium;sulfane;hydroxide Chemical compound O.[Na+].[SH-] ZNKXTIAQRUWLRL-UHFFFAOYSA-M 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
235000013599 spices Nutrition 0.000 description 1
230000028070 sporulation Effects 0.000 description 1
230000007480 spreading Effects 0.000 description 1
238000003892 spreading Methods 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
239000004575 stone Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
238000013268 sustained release Methods 0.000 description 1
239000012730 sustained-release form Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
238000001665 trituration Methods 0.000 description 1
239000013598 vector Substances 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
230000003612 virological effect Effects 0.000 description 1
239000003643 water by type Substances 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1
238000009736 wetting Methods 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
- 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
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- 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
- 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
- C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms

Landscapes

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

APAP/P/1999/001586A 1996-12-24 1997-12-18 Pesticidal 1-aryl and pyridylpyrazole derivatives. AP1004A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US3388596P	1996-12-24	1996-12-24
PCT/EP1997/007116 WO1998028279A1 (en)	1996-12-24	1997-12-18	Pesticidal 1-aryl and pyridylpyrazole derivatives

Publications (2)

Publication Number	Publication Date
AP9901586A0 AP9901586A0 (en)	1999-06-30
AP1004A true AP1004A (en)	2001-08-28

Family

ID=21873029

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
APAP/P/1999/001586A AP1004A (en)	1996-12-24	1997-12-18	Pesticidal 1-aryl and pyridylpyrazole derivatives.

Country Status (19)

Country	Link
EP (1)	EP0948487A1 (id)
JP (1)	JP2001506665A (id)
KR (1)	KR20000062318A (id)
AP (1)	AP1004A (id)
AU (1)	AU747450B2 (id)
BG (1)	BG103592A (id)
BR (1)	BR9714086A (id)
CA (1)	CA2275634A1 (id)
CZ (1)	CZ229999A3 (id)
EA (1)	EA003995B1 (id)
HU (1)	HUP0000464A3 (id)
ID (1)	ID22807A (id)
IL (1)	IL130537A (id)
NZ (1)	NZ336420A (id)
PL (1)	PL334237A1 (id)
SK (1)	SK284351B6 (id)
TR (1)	TR199901471T2 (id)
UA (1)	UA67734C2 (id)
WO (1)	WO1998028279A1 (id)

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FR2805971B1 (fr)	2000-03-08	2004-01-30	Aventis Cropscience Sa	Procedes de traitement et/ou de protection des cultures contre les arthropodes et compositions utiles pour de tels procedes
ZA200601794B (en) *	2003-09-04	2007-04-25	Bayer Cropscience Sa	Pesticidal 5-substituted-oxyalkylamino-1-arylpyrazole derivatives
PL1727805T3 (pl) *	2004-03-15	2009-01-30	Merial Ltd	Pochodne 1-fenylo i 1-pirydylopirazolu oraz ich zastosowanie jako pestycydów
US20050234119A1 (en) *	2004-04-16	2005-10-20	Soll Mark D	Antiparasitical agents and methods for treating, preventing and controlling external parasites in animals
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AR062844A1 (es)	2006-09-14	2008-12-10	Basf Ag	Composicion pesticida
UA110598C2 (uk)	2006-11-10	2016-01-25	Басф Се	Спосіб одержання кристалічної модифікації фіпронілу
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HRP20110641T4 (hr)	2006-11-10	2015-05-22	Basf Se	Kristalna modifikacija fipronila
ATE468748T1 (de)	2006-11-30	2010-06-15	Basf Se	Agrarchemikalienformulierungen, die n-vinylamid- copolymere enthalten
WO2008064990A2 (en)	2006-11-30	2008-06-05	Basf Se	Agrochemical formulations comprising l-vinyl-2 -pyrrolidinone co-polymers
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EP2258177A3 (en)	2006-12-15	2011-11-09	Rohm and Haas Company	Mixtures comprising 1-methylcyclopropene
DE102006061538A1 (de)	2006-12-27	2008-07-03	Bayer Healthcare Ag	Kombinationsprodukt zur Bekämpfung von Parasiten an Tieren
DE102006061537A1 (de)	2006-12-27	2008-07-03	Bayer Healthcare Ag	Mittel zur Bekämpfung von Parasiten an Tieren
US8211828B2 (en)	2007-01-19	2012-07-03	Basf Se	Fungicidal mixtures of 1-methylpyrazol-4-ylcarboxanilides and azolopyrimidinylamines
ES2383101T3 (es)	2007-01-26	2012-06-18	Basf Se	Compuestos de 3-amino-1,2-bencisotiazol para combatir plagas animales II
EP1952690A3 (en)	2007-01-31	2009-04-22	Basf Se	Pesticidal mixtures based on triazolopyrimidines and insecticides
CL2008000357A1 (es)	2007-02-06	2009-09-11	Basf Se	Agente que contiene al menos un antagonista de gaba, tal como fipronilo, al menos un fungicida de azol, tal como triconazol y al menos una giberelina; y su uso para mejorar la germinacion y/o la emergencia y/o vitalidad de las plantas.
EP2114163B1 (en)	2007-04-12	2017-05-10	Basf Se	Pesticidal mixtures comprising a cyanosulfoximine compound
CA2682294A1 (en)	2007-04-23	2008-10-30	Basf Se	Plant productivity enhancement by combining chemical agents with transgenic modifications
CL2008002420A1 (es)	2007-08-16	2009-10-23	Basf Se	Uso de una composicion que comprende a) un ingrediente activo seleccionado de piraclostrobina; b) un sulfato de eter poliarilfenol polialcoxi; y c) un co-polimero basado en esteres metaacrilicos para el tratamiento de semillas y composicion para el tratamiento de semillas.
HUE048086T2 (hu)	2007-09-20	2020-05-28	Bayer Cropscience Lp	Fungicid törzset és legalább egy további fungicidet tartalmazó kombinációk
JP2011510033A (ja)	2008-01-25	2011-03-31	シンジェンタパーティシペーションズアクチェンゲゼルシャフト	化合物
CA2749223C (en)	2009-01-27	2017-07-04	Basf Se	Method for dressing seeds
WO2010089244A1 (en)	2009-02-03	2010-08-12	Basf Se	Method for dressing seeds
JP2012519662A (ja)	2009-03-04	2012-08-30	ビーエーエスエフソシエタス・ヨーロピア	無脊椎有害生物を駆除するための３−アリールキナゾリン−４−オン化合物
ES2472918T3 (es)	2009-07-06	2014-07-03	Basf Se	Compuestos de piridazina para controlar plagas de invertebrados
WO2011117286A1 (en)	2010-03-23	2011-09-29	Basf Se	Pyridazine compounds for controlling invertebrate pests
US9925167B2 (en)	2011-06-30	2018-03-27	Hansen-Ab Gmbh	Agents for the control of parasites on animals
JO3626B1 (ar)	2012-02-23	2020-08-27	Merial Inc	تركيبات موضعية تحتوي على فيبرونيل و بيرميثرين و طرق استخدامها
AR100304A1 (es)	2014-02-05	2016-09-28	Basf Corp	Formulación de recubrimiento de semillas
WO2025242701A1 (en)	2024-05-22	2025-11-27	Basf Se	Seed treatment compositions

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1997
- 1997-12-18 SK SK856-99A patent/SK284351B6/sk not_active IP Right Cessation
- 1997-12-18 AP APAP/P/1999/001586A patent/AP1004A/en active
- 1997-12-18 ID IDW990586A patent/ID22807A/id unknown
- 1997-12-18 CZ CZ992299A patent/CZ229999A3/cs unknown
- 1997-12-18 KR KR1019997005757A patent/KR20000062318A/ko not_active Abandoned
- 1997-12-18 HU HU0000464A patent/HUP0000464A3/hu unknown
- 1997-12-18 JP JP52835198A patent/JP2001506665A/ja active Pending
- 1997-12-18 WO PCT/EP1997/007116 patent/WO1998028279A1/en not_active Ceased
- 1997-12-18 IL IL13053797A patent/IL130537A/en not_active IP Right Cessation
- 1997-12-18 CA CA002275634A patent/CA2275634A1/en not_active Abandoned
- 1997-12-18 EA EA199900598A patent/EA003995B1/ru not_active IP Right Cessation
- 1997-12-18 UA UA99074126A patent/UA67734C2/uk unknown
- 1997-12-18 NZ NZ336420A patent/NZ336420A/en unknown
- 1997-12-18 BR BR9714086-4A patent/BR9714086A/pt unknown
- 1997-12-18 AU AU57598/98A patent/AU747450B2/en not_active Ceased
- 1997-12-18 EP EP97953851A patent/EP0948487A1/en not_active Ceased
- 1997-12-18 TR TR1999/01471T patent/TR199901471T2/xx unknown
- 1997-12-18 PL PL97334237A patent/PL334237A1/xx unknown
1999
- 1999-07-19 BG BG103592A patent/BG103592A/xx unknown

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WO1993006089A1 (en) *	1991-09-27	1993-04-01	Zeneca Limited	N-phenylphrazoles as insecticides and acaricides
WO1994021606A1 (en) *	1993-03-25	1994-09-29	Zeneca Limited	Pentafluorosulphanylphenyl and pentafluorosulphanylpyridil substituted heteroaromatic compounds with insecticidal or acaricidal activity

Also Published As

Publication number	Publication date
JP2001506665A (ja)	2001-05-22
SK284351B6 (sk)	2005-02-04
EP0948487A1 (en)	1999-10-13
AU747450B2 (en)	2002-05-16
BG103592A (en)	2000-11-30
EA199900598A1 (ru)	2000-02-28
SK85699A3 (en)	2000-01-18
AP9901586A0 (en)	1999-06-30
WO1998028279A1 (en)	1998-07-02
CZ229999A3 (cs)	1999-11-17
BR9714086A (pt)	2000-05-09
HUP0000464A3 (en)	2002-01-28
HUP0000464A2 (hu)	2000-06-28
CA2275634A1 (en)	1998-07-02
NZ336420A (en)	2001-04-27
EA003995B1 (ru)	2003-12-25
AU5759898A (en)	1998-07-17
UA67734C2 (uk)	2004-07-15
KR20000062318A (ko)	2000-10-25
IL130537A (en)	2004-08-31
TR199901471T2 (xx)	1999-10-21
ID22807A (id)	1999-12-09
PL334237A1 (en)	2000-02-14
IL130537A0 (en)	2000-06-01

Publication	Publication Date	Title
AU747450B2 (en)	2002-05-16	Pesticidal 1-aryl and pyridylpyrazole derivatives
CA2275635C (en)	2008-11-25	Pesticidal 1-arylpyrazoles
US6350771B1 (en)	2002-02-26	Pesticidal 1-arylpyrazoles
AP1158A (en)	2003-06-30	Pesticidal 1- Aryl -3- Iminopyrazoles.
EP0973747B1 (en)	2003-10-15	Pesticidal 1-arylpyrazoles
US6638956B2 (en)	2003-10-28	Pesticidal 1-arylpyrazoles
US6008353A (en)	1999-12-28	Pesticidal 1-arylpyrazole boranes
US20020016468A1 (en)	2002-02-07	Pesticidal 1-arylpyrazole derivatives