UA80731C2 - Fungicidal mixture based on triazolopyrimidines and azoles, fungicidal agent, controlling method, seed and using compounds - Google Patents

Fungicidal mixture based on triazolopyrimidines and azoles, fungicidal agent, controlling method, seed and using compounds Download PDF

Info

Publication number: UA80731C2
Authority: UA; Ukraine
Prior art keywords: formula; fungicidal; compounds; mixtures; triazolopyrimidine
Prior art date: 2002-11-15

Application number

UAA200505922A

Other languages

English (en)

Ukrainian (uk)

Inventor

Thomas Grotte

Eberhard Ammermann

Reinhard Stierl

Siegfried Strathmann

Ulrich Schoefl

Original Assignee

Basf 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.)

2002-11-15

Filing date

2003-11-14

Publication date

2007-10-25

2003-11-14 Application filed by Basf Ag filed Critical Basf Ag

2007-10-25 Publication of UA80731C2 publication Critical patent/UA80731C2/uk

Links

239000000203 mixture Substances 0.000 title claims abstract description 77
150000001875 compounds Chemical class 0.000 title claims abstract description 51
230000000855 fungicidal effect Effects 0.000 title claims abstract description 17
238000000034 method Methods 0.000 title claims abstract description 9
239000000417 fungicide Substances 0.000 title claims description 11
150000003851 azoles Chemical class 0.000 title description 3
YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical class BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 claims abstract description 27
241000233866 Fungi Species 0.000 claims abstract description 25
-1 fluzylazole Chemical compound 0.000 claims abstract description 18
WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims abstract description 9
MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 claims abstract description 9
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WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
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235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
241000219122 Cucurbita Species 0.000 description 1
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241000238631 Hexapoda Species 0.000 description 1
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235000019738 Limestone Nutrition 0.000 description 1
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240000005561 Musa balbisiana Species 0.000 description 1
235000018290 Musa x paradisiaca Nutrition 0.000 description 1
241000244206 Nematoda Species 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
241000209056 Secale Species 0.000 description 1
235000007238 Secale cereale Nutrition 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
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
OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
230000003044 adaptive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 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
DVARTQFDIMZBAA-UHFFFAOYSA-O ammonium nitrate Chemical class [NH4+].[O-][N+]([O-])=O DVARTQFDIMZBAA-UHFFFAOYSA-O 0.000 description 1
ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical class [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
235000019289 ammonium phosphates Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical class N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
235000021016 apples Nutrition 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
239000010426 asphalt Substances 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
239000003637 basic solution Substances 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
238000009835 boiling Methods 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
239000011651 chromium Substances 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
235000016213 coffee Nutrition 0.000 description 1
235000013353 coffee beverage Nutrition 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
125000004122 cyclic group Chemical group 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
231100000676 disease causative agent Toxicity 0.000 description 1
239000004491 dispersible concentrate Substances 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
235000012055 fruits and vegetables Nutrition 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
238000000227 grinding Methods 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
229940071870 hydroiodic acid Drugs 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000006028 limestone Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [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
230000007246 mechanism Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
239000010742 number 1 fuel oil Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
239000004550 soluble concentrate Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000004552 water soluble powder Substances 0.000 description 1
239000003021 water soluble solvent 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

- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
- 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<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof

Landscapes

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)

UAA200505922A 2002-11-15 2003-11-14 Fungicidal mixture based on triazolopyrimidines and azoles, fungicidal agent, controlling method, seed and using compounds UA80731C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10253584		2002-11-15
PCT/EP2003/012767 WO2004064519A1 (de)	2002-11-15	2003-11-14	Fungizide mischungen auf der basis eines triazolopyrimidin-derivates und azolen

Publications (1)

Publication Number	Publication Date
UA80731C2 true UA80731C2 (en)	2007-10-25

Family

ID=32747416

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UAA200505922A UA80731C2 (en)	2002-11-15	2003-11-14	Fungicidal mixture based on triazolopyrimidines and azoles, fungicidal agent, controlling method, seed and using compounds

Country Status (26)

Country	Link
US (1)	US20060111320A1 (es)
EP (1)	EP1562428A1 (es)
JP (1)	JP2006517521A (es)
KR (1)	KR100717675B1 (es)
CN (1)	CN1711019A (es)
AP (1)	AP2005003312A0 (es)
AR (1)	AR042055A1 (es)
AU (1)	AU2003303097A1 (es)
BR (1)	BR0316273A (es)
CA (1)	CA2505588A1 (es)
CO (1)	CO5570637A2 (es)
CR (1)	CR7837A (es)
EA (1)	EA200500722A1 (es)
EC (1)	ECSP055760A (es)
EG (1)	EG23743A (es)
HR (1)	HRP20050550A2 (es)
MA (1)	MA27494A1 (es)
MX (1)	MXPA05004548A (es)
NO (1)	NO20051926L (es)
OA (1)	OA12956A (es)
PL (1)	PL377178A1 (es)
RS (1)	RS20050358A (es)
TW (1)	TW200505342A (es)
UA (1)	UA80731C2 (es)
WO (1)	WO2004064519A1 (es)
ZA (1)	ZA200504842B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EA200600615A1 (ru) *	2003-10-01	2006-08-25	Басф Акциенгезельшафт	Фунгицидные смеси
WO2007141010A1 (en) *	2006-06-08	2007-12-13	Syngenta Participations Ag,	A method of protecting a plant propagation material, a plant, parts of a plant and/or plant organs
CN101617669B (zh) *	2009-07-28	2012-07-04	陕西汤普森生物科技有限公司	一种含氟菌唑与戊唑醇的杀菌组合物
CN102165957B (zh) *	2011-03-05	2014-03-05	陕西美邦农药有限公司	一种含有腈苯唑与三唑类化合物的增效杀菌组合物
GB201610264D0 (en) *	2016-06-13	2016-07-27	Syngenta Participations Ag	Pesticidal compositions

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1469772A (en) *	1973-06-21	1977-04-06	Boots Co Ltd	Fungicidal imidazole derivatives
DE4130298A1 (de) *	1991-09-12	1993-03-18	Basf Ag	Fungizide mischungen
EP0645091B1 (de) *	1993-09-24	1996-04-17	BASF Aktiengesellschaft	Fungizide Mischungen
EP0844818B1 (de) *	1995-08-17	1999-09-22	Basf Aktiengesellschaft	Fungizide mischungen eines oximethercarbonsäureamids mit azolderivaten
JPH0988790A (ja) *	1995-09-29	1997-03-31	Nissan Motor Co Ltd	内燃機関の電子制御装置
TWI252231B (en) *	1997-04-14	2006-04-01	American Cyanamid Co	Fungicidal trifluorophenyl-triazolopyrimidines
US6268371B1 (en) *	1998-09-10	2001-07-31	American Cyanamid Co.	Fungicidal mixtures
ES2203021T3 (es) *	1998-09-25	2004-04-01	Basf Aktiengesellschaft	Mezclas fungicidas.
EA200401291A1 (ru) *	2002-04-05	2005-02-24	Басф Акциенгезельшафт	Фунгицидная смесь на базе производных бензамидоксима и азолов

2003
- 2003-11-14 HR HR20050550A patent/HRP20050550A2/hr not_active Application Discontinuation
- 2003-11-14 OA OA1200500138A patent/OA12956A/en unknown
- 2003-11-14 KR KR1020057008581A patent/KR100717675B1/ko not_active Expired - Fee Related
- 2003-11-14 UA UAA200505922A patent/UA80731C2/uk unknown
- 2003-11-14 EP EP03814404A patent/EP1562428A1/de not_active Withdrawn
- 2003-11-14 JP JP2004566760A patent/JP2006517521A/ja not_active Withdrawn
- 2003-11-14 RS YUP-2005/0358A patent/RS20050358A/sr unknown
- 2003-11-14 AP AP2005003312A patent/AP2005003312A0/xx unknown
- 2003-11-14 CA CA002505588A patent/CA2505588A1/en not_active Abandoned
- 2003-11-14 MX MXPA05004548A patent/MXPA05004548A/es not_active Application Discontinuation
- 2003-11-14 EA EA200500722A patent/EA200500722A1/ru unknown
- 2003-11-14 AU AU2003303097A patent/AU2003303097A1/en not_active Abandoned
- 2003-11-14 US US10/532,755 patent/US20060111320A1/en not_active Abandoned
- 2003-11-14 BR BR0316273-7A patent/BR0316273A/pt not_active IP Right Cessation
- 2003-11-14 PL PL377178A patent/PL377178A1/pl not_active Application Discontinuation
- 2003-11-14 CN CNA2003801032118A patent/CN1711019A/zh active Pending
- 2003-11-14 WO PCT/EP2003/012767 patent/WO2004064519A1/de not_active Ceased
- 2003-11-17 AR ARP030104240A patent/AR042055A1/es not_active Application Discontinuation
- 2003-11-17 TW TW092132370A patent/TW200505342A/zh unknown
2005
- 2005-04-20 NO NO20051926A patent/NO20051926L/no not_active Application Discontinuation
- 2005-04-26 EC EC2005005760A patent/ECSP055760A/es unknown
- 2005-05-03 EG EGNA2005000186 patent/EG23743A/xx active
- 2005-05-11 CR CR7837A patent/CR7837A/es not_active Application Discontinuation
- 2005-05-30 MA MA28304A patent/MA27494A1/fr unknown
- 2005-06-14 CO CO05057637A patent/CO5570637A2/es not_active Application Discontinuation
- 2005-06-14 ZA ZA200504842A patent/ZA200504842B/en unknown

Also Published As

Publication number	Publication date
OA12956A (en)	2006-10-13
EA200500722A1 (ru)	2005-12-29
JP2006517521A (ja)	2006-07-27
CA2505588A1 (en)	2004-08-05
BR0316273A (pt)	2005-10-11
HRP20050550A2 (en)	2005-10-31
AR042055A1 (es)	2005-06-08
ZA200504842B (en)	2006-08-30
AU2003303097A1 (en)	2004-08-13
KR100717675B1 (ko)	2007-05-14
KR20050075002A (ko)	2005-07-19
RS20050358A (sr)	2007-11-15
US20060111320A1 (en)	2006-05-25
CN1711019A (zh)	2005-12-21
EG23743A (en)	2007-07-29
EP1562428A1 (de)	2005-08-17
MXPA05004548A (es)	2005-07-26
TW200505342A (en)	2005-02-16
MA27494A1 (fr)	2005-08-01
WO2004064519A1 (de)	2004-08-05
PL377178A1 (pl)	2006-01-23
CR7837A (es)	2007-11-23
ECSP055760A (es)	2006-04-19
AP2005003312A0 (en)	2005-06-30
CO5570637A2 (es)	2005-10-31
NO20051926L (no)	2005-06-14

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UA78554C2 (en)	2007-04-10	Fungicidal mixture on the base of prothioconazole with insecticide, method for controlling phytopathogenic fungi
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