BG62077B1 - Нови 3-фенилпиразолови производни и използването им катофунгициди - Google Patents

Нови 3-фенилпиразолови производни и използването им катофунгициди Download PDF

Info

Publication number: BG62077B1
Authority: BG; Bulgaria
Prior art keywords: halogen; hydrogen; water; nitro; derivatives
Prior art date: 1994-07-13

Application number

BG101207A

Other languages

Bulgarian (bg)

English (en)

Other versions

BG101207A (en

Inventor

Richard Cantegril

Jacques Mortier

Denis Croisat

Raymond Peignier

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.)

1994-07-13

Filing date

1997-02-07

Publication date

1999-02-26

1997-02-07 Application filed by Rhone-Poulenc Agrochimie filed Critical Rhone-Poulenc Agrochimie

1997-08-29 Publication of BG101207A publication Critical patent/BG101207A/xx

1999-02-26 Publication of BG62077B1 publication Critical patent/BG62077B1/bg

Links

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GDUANFXPOZTYKS-UHFFFAOYSA-N 6-bromo-8-[(2,6-difluoro-4-methoxybenzoyl)amino]-4-oxochromene-2-carboxylic acid Chemical compound FC1=CC(OC)=CC(F)=C1C(=O)NC1=CC(Br)=CC2=C1OC(C(O)=O)=CC2=O GDUANFXPOZTYKS-UHFFFAOYSA-N 0.000 description 1
241001465180 Botrytis Species 0.000 description 1
NJNQNGFWWPCEGJ-UHFFFAOYSA-N C1=CC=C(C(=C1)C2=C(C=NN2)Cl)N Chemical class C1=CC=C(C(=C1)C2=C(C=NN2)Cl)N NJNQNGFWWPCEGJ-UHFFFAOYSA-N 0.000 description 1
ITKRKSNBSIUDMP-UHFFFAOYSA-N CC=1C=C(C=C(C=1F)C)C(C(=CN(C)C)Cl)=O Chemical compound CC=1C=C(C=C(C=1F)C)C(C(=CN(C)C)Cl)=O ITKRKSNBSIUDMP-UHFFFAOYSA-N 0.000 description 1
206010021033 Hypomenorrhoea Diseases 0.000 description 1
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
241000233654 Oomycetes Species 0.000 description 1
239000004435 Oxo alcohol Substances 0.000 description 1
241001123569 Puccinia recondita Species 0.000 description 1
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
240000006365 Vitis vinifera Species 0.000 description 1
235000014787 Vitis vinifera Nutrition 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
239000012346 acetyl chloride Substances 0.000 description 1
230000021736 acetylation Effects 0.000 description 1
238000006640 acetylation reaction Methods 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
229940126543 compound 14 Drugs 0.000 description 1
229940125758 compound 15 Drugs 0.000 description 1
229940125782 compound 2 Drugs 0.000 description 1
229940125846 compound 25 Drugs 0.000 description 1
238000007906 compression Methods 0.000 description 1
230000006835 compression Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
239000010949 copper Substances 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
230000006378 damage Effects 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
238000005202 decontamination Methods 0.000 description 1
230000003588 decontaminative effect Effects 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
150000001989 diazonium salts Chemical class 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000003623 enhancer Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000000499 gel Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
235000002532 grape seed extract Nutrition 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
239000005457 ice water Substances 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
229910052751 metal Chemical class 0.000 description 1
239000002184 metal Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
YGBMCLDVRUGXOV-UHFFFAOYSA-N n-[6-[6-chloro-5-[(4-fluorophenyl)sulfonylamino]pyridin-3-yl]-1,3-benzothiazol-2-yl]acetamide Chemical compound C1=C2SC(NC(=O)C)=NC2=CC=C1C(C=1)=CN=C(Cl)C=1NS(=O)(=O)C1=CC=C(F)C=C1 YGBMCLDVRUGXOV-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
238000006396 nitration reaction Methods 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
230000035515 penetration Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229940044654 phenolsulfonic acid Drugs 0.000 description 1
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
150000003017 phosphorus Polymers 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000013138 pruning Methods 0.000 description 1
150000003217 pyrazoles Chemical class 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000007873 sieving Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000758 substrate Substances 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
230000009974 thixotropic effect Effects 0.000 description 1
GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
238000001665 trituration Methods 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000004562 water dispersible granule Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1

Classifications

- 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
- C07D231/16—Halogen atoms or nitro radicals

Landscapes

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

BG101207A 1994-07-13 1997-02-07 Нови 3-фенилпиразолови производни и използването им катофунгициди BG62077B1 (bg)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR9408936A FR2722369B1 (fr)	1994-07-13	1994-07-13	Compositions fongicides a base de derives 3-phenyl-pyrazoles pour le traitement du materiel vegetal de multiplication, nouveaux derives 3-phenyl-pyrazoles et leurs applications fongicides
PCT/FR1995/000921 WO1996002138A1 (fr)	1994-07-13	1995-07-10	Compositions fongicides a base de derives 3-phenyl-pyrazoles pour le traitement du materiel vegetal de multiplication, nouveaux derives 3-phenyl-pyrazoles et leurs applications fongicides

Publications (2)

Publication Number	Publication Date
BG101207A BG101207A (en)	1997-08-29
BG62077B1 true BG62077B1 (bg)	1999-02-26

Family

ID=9465542

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BG101207A BG62077B1 (bg)	1994-07-13	1997-02-07	Нови 3-фенилпиразолови производни и използването им катофунгициди

Country Status (18)

Country	Link
EP (1)	EP0769905A1 (sv)
JP (1)	JPH10502661A (sv)
KR (1)	KR970704349A (sv)
CN (1)	CN1152853A (sv)
AU (1)	AU2931295A (sv)
BG (1)	BG62077B1 (sv)
BR (1)	BR9508790A (sv)
CA (1)	CA2194913A1 (sv)
CO (1)	CO4480715A1 (sv)
CZ (1)	CZ9197A3 (sv)
FI (1)	FI970099L (sv)
FR (1)	FR2722369B1 (sv)
HU (1)	HUT76819A (sv)
MX (1)	MX9700297A (sv)
PL (1)	PL318161A1 (sv)
SK (1)	SK4697A3 (sv)
WO (1)	WO1996002138A1 (sv)
ZA (1)	ZA955518B (sv)

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WO1996024589A1 (fr) *	1995-02-07	1996-08-15	Nissan Chemical Industries, Ltd.	Derives et herbicides a base de pyrazole
WO1998043480A1 (fr) *	1997-03-28	1998-10-08	Rhone-Poulenc Agro	Compositions fongicides comprenant un 3-phenyl-pyrazole
MXPA02008780A (es) *	2000-03-16	2003-02-12	Basf Ag	Preparacion de 7-(pirazol-3-il)benzoxazoles.
EE05400B1 (et)	2001-04-10	2011-04-15	Pfizer Inc.	Prasoolderivaadid, neid v?i nende farmatseutiliselt vastuv?etavaid sooli, solvaate v?i derivaate sisaldavad farmatseutilised kompositsioonid, nende kasutamine ning meetodid nende valmistamiseks
ATE313532T1 (de)	2003-07-22	2006-01-15	Arena Pharm Inc	Diaryl- und arylheteroarylharnstoffderivate als modulatoren des 5-ht2a-serotoninrezeptors, die sich zur prophylaxe und behandlung von damit im zusammenhang stehenden erkrankungen eignen
CA2559038C (en) *	2004-03-23	2013-09-10	Arena Pharmaceuticals, Inc.	Processes for preparing substituted n-aryl-n'-[3-(1h-pyrazol-5-yl) phenyl] ureas and intermediates thereof
SA05260357B1 (ar)	2004-11-19	2008-09-08	ارينا فارماسيتو تيكالز ، أنك	مشتقات 3_فينيل_بيرازول كمعدلات لمستقبل سيروتينين 5_ht2a مفيدة في علاج الاضطرابات المتعلقه به
SE528817C2 (sv)	2005-05-23	2007-02-20	Camfil Ab	Påsfilteraggregat
WO2007136680A2 (en)	2006-05-18	2007-11-29	Arena Pharmaceuticals, Inc.	3-pyraz0lyl-benzamide-4-ethers, secondary amines and derivatives thereof as modulators of the 5-ht2a serotonin receptor useful for the treatment of disorders related thereto
BRPI0712030A2 (pt)	2006-05-18	2012-01-03	Arena Pharm Inc	formas cristalinas e processos para preparaÇço de fenil-pirazàis éteis como moduladores dos receptores de serotonina 5-h-t2a
USRE45336E1 (en)	2006-05-18	2015-01-13	Arena Pharmaceuticals, Inc.	Primary amines and derivatives thereof as modulators of the 5-HT2A serotonin receptor useful for the treatment of disorders related thereto
TWI415845B (zh)	2006-10-03	2013-11-21	Arena Pharm Inc	用於治療與５-ｈｔ2ａ血清素受體相關聯病症之作為５-ｈｔ2ａ血清素受體之調節劑的吡唑衍生物
WO2009023253A2 (en)	2007-08-15	2009-02-19	Arena Pharmaceuticals Inc.	IMIDAZO[L,2-α]PYRIDINE DERIVATIVES AS MODULATORS OF THE 5-HT2A SEROTONIN RECEPTOR USEFUL FOR THE TREATMENT OF DISORDERS RELATED THERETO
US20110021538A1 (en)	2008-04-02	2011-01-27	Arena Pharmaceuticals, Inc.	Processes for the preparation of pyrazole derivatives useful as modulators of the 5-ht2a serotonin receptor
HUE036506T2 (hu)	2008-10-28	2018-07-30	Arena Pharm Inc	5-HT2A szerotonin receptor modulátort tartalmazó készítmények az ilyen receptor modulátorokkal kapcsolatos rendellenességek kezelésére
WO2010062321A1 (en)	2008-10-28	2010-06-03	Arena Pharmaceuticals, Inc.	Processes useful for the preparation of 1-[3-(4-bromo-2-methyl-2h-pyrazol-3-yl)-4-methoxy-phenyl]-3-(2,4-difluoro-phenyl)-urea and crystalline forms related thereto
US8980891B2 (en)	2009-12-18	2015-03-17	Arena Pharmaceuticals, Inc.	Crystalline forms of certain 3-phenyl-pyrazole derivatives as modulators of the 5-HT2A serotonin receptor useful for the treatment of disorders related thereto
TWI504350B (zh)	2010-09-01	2015-10-21	Du Pont	殺真菌吡唑及其混合物
CA2989343A1 (en)	2015-06-12	2016-12-15	Yandong Wen	Diaryl and arylheteroaryl urea derivatives useful for the prophylaxis and treatment of rem sleep behavior disorder
JP2018520187A (ja)	2015-07-15	2018-07-26	アクソヴァントサイエンシーズゲゼルシャフトミットベシュレンクテルハフツングAxovant Sciences GmbH	神経変性疾患と関連する幻覚の予防および処置のために有用な５−ｈｔ２ａセロトニン受容体のモジュレーターとしてのジアリールおよびアリールヘテロアリール尿素誘導体
CN112839505B (zh) *	2018-10-18	2023-06-06	住友化学株式会社	苯基吡唑化合物及植物病害防除方法
AR121893A1 (es) *	2020-04-22	2022-07-20	Sumitomo Chemical Co	Compuesto de fenilo y método para controlar enfermedades vegetales
AR130609A1 (es)	2022-09-30	2024-12-18	Sumitomo Chemical Co	Compuesto de fenilpirazol y método para controlar enfermedades vegetales

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FR2682379B1 (fr) *	1991-10-09	1994-02-11	Rhone Poulenc Agrochimie	Nouveaux phenylpyrazoles fongicides.
FR2690440B1 (fr) *	1992-04-27	1995-05-19	Rhone Poulenc Agrochimie	Arylpyrazoles fongicides.

1994
- 1994-07-13 FR FR9408936A patent/FR2722369B1/fr not_active Expired - Fee Related
1995
- 1995-07-03 ZA ZA955518A patent/ZA955518B/xx unknown
- 1995-07-10 EP EP95925032A patent/EP0769905A1/fr not_active Withdrawn
- 1995-07-10 CZ CZ9791A patent/CZ9197A3/cs unknown
- 1995-07-10 HU HU9700092A patent/HUT76819A/hu unknown
- 1995-07-10 WO PCT/FR1995/000921 patent/WO1996002138A1/fr not_active Application Discontinuation
- 1995-07-10 CA CA002194913A patent/CA2194913A1/fr not_active Abandoned
- 1995-07-10 CN CN95194108A patent/CN1152853A/zh active Pending
- 1995-07-10 MX MX9700297A patent/MX9700297A/es unknown
- 1995-07-10 BR BR9508790A patent/BR9508790A/pt unknown
- 1995-07-10 JP JP8504744A patent/JPH10502661A/ja active Pending
- 1995-07-10 AU AU29312/95A patent/AU2931295A/en not_active Abandoned
- 1995-07-10 PL PL95318161A patent/PL318161A1/xx unknown
- 1995-07-10 SK SK46-97A patent/SK4697A3/sk unknown
- 1995-07-10 KR KR1019970700203A patent/KR970704349A/ko not_active Application Discontinuation
- 1995-07-11 CO CO95030223A patent/CO4480715A1/es unknown
1997
- 1997-01-10 FI FI970099A patent/FI970099L/sv unknown
- 1997-02-07 BG BG101207A patent/BG62077B1/bg unknown

Also Published As

Publication number	Publication date
HUT76819A (en)	1997-11-28
FI970099A0 (sv)	1997-01-10
ZA955518B (en)	1996-10-24
BR9508790A (pt)	1997-12-30
BG101207A (en)	1997-08-29
CN1152853A (zh)	1997-06-25
MX9700297A (es)	1997-05-31
CA2194913A1 (fr)	1996-02-01
KR970704349A (ko)	1997-09-06
JPH10502661A (ja)	1998-03-10
FR2722369B1 (fr)	1998-07-10
CO4480715A1 (es)	1997-07-09
CZ9197A3 (en)	1997-04-16
SK4697A3 (en)	1997-09-10
FR2722369A1 (fr)	1996-01-19
EP0769905A1 (fr)	1997-05-02
PL318161A1 (en)	1997-05-26
FI970099L (sv)	1997-03-10
WO1996002138A1 (fr)	1996-02-01
AU2931295A (en)	1996-02-16

Publication	Publication Date	Title
BG62077B1 (bg)	1999-02-26	Нови 3-фенилпиразолови производни и използването им катофунгициди
JP2793956B2 (ja)	1998-09-03	トリアジン誘導体およびそれを有効成分とする除草剤
EP1845086B1 (en)	2013-04-24	N-(2-substituted phenyl)-N-methoxycarbamates and their preparation and use thereof
JP3002786B2 (ja)	2000-01-24	有害生物防除組成物
US5945382A (en)	1999-08-31	Fungicidal arylpyrazoles
SK306592A3 (en)	1995-10-11	3-phenylpyrazole derivatives, method of their preparation and fungicidal compositions containing them
DE3013162A1 (de)	1980-10-30	N-substituierte tetrahydrophthalimide und herbizide mittel mit einem gehalt derselben
US4622323A (en)	1986-11-11	Fungicidal 2-cyanobenzimidazole derivatives
EP0126254A1 (de)	1984-11-28	N-(2-Nitrophenyl)-4-aminopyrimidin-Derivate als Mikrobizide
CZ128493A3 (en)	1994-01-19	Phenylbenzamides, process of their preparation and fungicidal composition in which they are comprised
JPS60166665A (ja)	1985-08-29	テトラヒドロ−２ｈ−インダゾ−ル誘導体、その製造法およびそれを有効成分とする除草剤
JPS6223752B2 (sv)	1987-05-25
NO862231L (no)	1986-12-05	Fungicide midler.
JPS6299368A (ja)	1987-05-08	Δ↑２−１，２，４−トリアゾリン−５−オン誘導体及びその製法並びにその用途
JPS62205063A (ja)	1987-09-09	新規な２−シアノベンゾイミダゾ−ル誘導体、その製造方法および殺菌剤としてのその使用、並びに他の殺菌剤との組合せ物
EP0288976A2 (de)	1988-11-02	Mittel zum Schutz gegen Pflanzenkrankheiten
US4942178A (en)	1990-07-17	Plant protection agents for control of fungi
US4405743A (en)	1983-09-20	Pyrazolylpyrimidine derivatives
JP2504072B2 (ja)	1996-06-05	置換ベンゾイル誘導体および除草剤
JPH0576477B2 (sv)	1993-10-22
JPH01157965A (ja)	1989-06-21	殺菌性ピリジルカルバメート及びそれらの塩
DE2129524C3 (de)	1981-07-23	Fungizide Mittel auf Basis von Phenylhydrazono-imid azolenin-Derivaten
JPS61280471A (ja)	1986-12-11	テトラヒドロフタルイミド誘導体およびそれを有効成分とする除草剤
JPH0226632B2 (sv)	1990-06-12
CH631602A5 (en)	1982-08-31	Microbicides