RU97112090A - FUNGICIDAL MIXTURE - Google Patents

FUNGICIDAL MIXTURE

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Publication number
RU97112090A
RU97112090A RU97112090/04A RU97112090A RU97112090A RU 97112090 A RU97112090 A RU 97112090A RU 97112090/04 A RU97112090/04 A RU 97112090/04A RU 97112090 A RU97112090 A RU 97112090A RU 97112090 A RU97112090 A RU 97112090A
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RU
Russia
Prior art keywords
formula
compounds
alkyl
alkoxy
haloalkyl
Prior art date
Application number
RU97112090/04A
Other languages
Russian (ru)
Other versions
RU2176138C2 (en
Inventor
Вагнер Оливер
Айкен Карл
Байер Герберт
Заутер Губерт
Аммерманн Эберхард
Лоренц Гизела
Original Assignee
Басф Акциенгезельшафт
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.)
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Publication date
Priority claimed from DE4444911A external-priority patent/DE4444911A1/en
Application filed by Басф Акциенгезельшафт filed Critical Басф Акциенгезельшафт
Publication of RU97112090A publication Critical patent/RU97112090A/en
Application granted granted Critical
Publication of RU2176138C2 publication Critical patent/RU2176138C2/en

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Claims (8)

1. Фунгицидная смесь, содержащая синергически эффективное количество
а) соединения формулы I
Figure 00000001

его N-оксида или одной из его солей, где радикалы имеют следующее значение: R1, R2, R3 и R4 независимо друг от друга означают водород, гидрокси, нитро, галоген, C1 - C4-алкил, C1 - C4-галогеналкил, C1 - C4-алкокси, C1 - C4-галогеналкокси, C1 - C4-алкилтио, C1 - C4-галогеналкилтио;
R5, R6 и R7 независимо друг от друга означают водород, гидрокси, циано, нитро, галоген, C1 - C7-алкил, C1 - C7-галогеналкил, C1 - C7-алкокси, C1 - C7-галогеналкокси, C1 - C7-алкилтио, C1 - C7-галогеналкилтио, C1 - C7-гидроксиалкил, C2 - C4-ацил, арил, арилокси, причем радикалы с арилом могут нести в свою очередь от одной до трех групп из числа следующих: циано, нитро, галоген, C1 - C4-алкил, C1 - C4-галогеналкил, C1 - C4-алкокси, C1 - C4-галогеналкокси, C1 - C4-алкилтио и C1 - C4-галогеналкилтио, и
б) соединения формулы II
Figure 00000002

в которой радикалы имеют следующее значение: R8 означает фенил, который может нести от одной до трех групп из числа следующих: циано, галоген, C1 - C4-алкил, C1 - C4-галогеналкил, C1 - C4-алкокси, или пиримидил, который может нести C1 - C3-алкильную группу и/или феноксигруппу, причем феноксигруппа может нести в свою очередь от одного до трех заместителей из числа следующих: циано, галоген, C1 - C4-алкил, C1 - C4-галогеналкил, C1 - C4-алкокси;
A означает кислород или оксиметилен (-OCH2-);
X означает CH или N;
Y означает кислород или NR, где R представляет собой водород, C1 - C3-алкил либо C1 - C3-алкокси, или
в) производного пиримидина формулы III
Figure 00000003

или одной из его солей, где радикал R9 представляет собой метил, пропин-1-ил либо циклопропил, или
г) (2SR, 3SR)-1-[3-(2-хлорфенил)-2-(4-фторфенил)оксиран-2-илметил]-1H-1,2,4-триазола формулы IV
Figure 00000004

или д) соединения формулы V
Figure 00000005

в которой радикалы имеют следующие значение: R10 означает фтор или хлор;
R11 означает трифторметил или хлор либо
R10 и R11 оба вместе представляют собой группу -OCF2O-.1. Fungicidal mixture containing a synergistically effective amount
a) compounds of formula I
Figure 00000001

its N-oxide or one of its salts, where the radicals have the following meaning: R 1 , R 2 , R 3 and R 4 independently from each other mean hydrogen, hydroxy, nitro, halogen, C 1 - C 4 -alkyl, C 1 - C 4 haloalkyl, C 1 - C 4 alkoxy, C 1 - C 4 haloalkoxy, C 1 - C 4 alkylthio, C 1 - C 4 haloalkylthio;
R 5 , R 6 and R 7 independently from each other mean hydrogen, hydroxy, cyano, nitro, halogen, C 1 - C 7 -alkyl, C 1 - C 7 -haloalkyl, C 1 - C 7 -alkoxy, C 1 - C 7 haloalkoxy, C 1 - C 7 alkylthio, C 1 - C 7 haloalkylthio, C 1 - C 7 hydroxyalkyl, C 2 - C 4 acyl, aryl, aryloxy, and radicals with aryl can in turn carry from one to three groups of the following: cyano, nitro, halogen, C 1 - C 4 -alkyl, C 1 - C 4 -haloalkyl, C 1 - C 4 -alkoxy, C 1 - C 4 -haloalkoxy, C 1 - C 4 -alkylthio and C 1 -C 4 -haloalkylthio; and
b) compounds of formula II
Figure 00000002

in which the radicals have the following meaning: R 8 means phenyl, which can carry from one to three groups of the following: cyano, halogen, C 1 - C 4 -alkyl, C 1 - C 4 -haloalkyl, C 1 - C 4 - alkoxy, or pyrimidyl, which can carry a C 1 - C 3 -alkyl group and / or phenoxy group, and the phenoxy group can in turn carry from one to three substituents from the following: cyano, halogen, C 1 -C 4 -alkyl, C 1 - C 4 haloalkyl; C 1 - C 4 alkoxy;
A is oxygen or oxymethylene (—OCH 2 -);
X is CH or N;
Y is oxygen or NR, where R is hydrogen, C 1 -C 3 alkyl or C 1 -C 3 alkoxy, or
c) a pyrimidine derivative of the formula III
Figure 00000003

or one of its salts, where the radical R 9 represents methyl, propin-1-yl or cyclopropyl, or
g) (2SR, 3SR) -1- [3- (2-chlorophenyl) -2- (4-fluorophenyl) oxiran-2-ylmethyl] -1H-1,2,4-triazole of formula IV
Figure 00000004

or e) compounds of formula V
Figure 00000005

in which the radicals have the following meanings: R 10 means fluorine or chlorine;
R 11 means trifluoromethyl or chlorine or
R 10 and R 11 both together represent a —OCF 2 O— group. 2. Фунгицидная смесь по п.1, отличающаяся тем, что соотношение по массе между соединением формулы I и соединениями формул II - V составляет 10 : 1 - 0,1 : 1. 2. The fungicidal mixture according to claim 1, characterized in that the mass ratio between the compound of formula I and the compounds of formulas II - V is 10: 1 - 0.1: 1. 3. Способ борьбы с вредоносными грабами, отличающийся тем, что грибы, среду их обитания или требующие защиты от поражения ими растения, семена, почву, площади, материалы или помещения обрабатывают соединением формулы I по п.1 и одним из соединений формулы II - V по п.1. 3. A method of combating harmful hornbeam, characterized in that the fungi, their habitat, or requiring protection from plants, seeds, soil, areas, materials or premises are treated with the compound of formula I according to claim 1 and one of the compounds of formula II - V according to claim 1. 4. Способ по п.3, отличающийся тем, что соединение формулы I и соединения формул II - V применяют для одновременной, а именно, совместно либо раздельно, или для последовательной обработки. 4. The method according to claim 3, characterized in that the compound of formula I and the compounds of formulas II - V are used for simultaneous, namely, jointly or separately, or for sequential processing. 5. Способ по п.3, отличающийся тем, что вредоносные грибы, среду их обитания или требующие защиты от поражения ими растения, семена, почву, площади, материалы или помещения обрабатывают соединением формулы I по п.1 с нормой расхода 0,01 - 0,5 кг/га. 5. The method according to claim 3, characterized in that the harmful fungi, their habitat, or requiring protection against damage from plants, seeds, soil, areas, materials or premises are treated with a compound of formula I according to claim 1 with a flow rate of 0.01 - 0.5 kg / ha. 6. Способ по п. 5, отличающийся тем, что вредоносные грибы, среду их обитания или требующие защиты от поражения ими растения, семена, почву, площади, материалы или помещения обрабатывают соединением формулы I по п.1 с нормой расхода 0,1 - 1 кг/га. 6. The method according to p. 5, characterized in that the harmful fungi, their habitat or requiring protection from damage by plants, seeds, soil, areas, materials or premises are treated with a compound of formula I according to claim 1 with a flow rate of 0.1 - 1 kg / ha. 7. Применение соединений формулы I по п.1 для получения обладающих фунгицидным действием синергических смесей по п.1. 7. The use of compounds of formula I according to claim 1 for the preparation of fungicidal synergistic mixtures according to claim 1. 8. Применение одного из соединений формул II - V по п.1 для получения обладающих фунгицидным действием синергических смесей по п.1. 8. The use of one of the compounds of formulas II - V according to claim 1 for obtaining synergistic mixtures having a fungicidal effect according to claim 1.
RU97112090/04A 1994-12-16 1995-12-05 Fungicide mixture and method of control of deleterious fungi RU2176138C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4444911A DE4444911A1 (en) 1994-12-16 1994-12-16 Fungicidal mixture
DEP4444911.9 1994-12-16

Publications (2)

Publication Number Publication Date
RU97112090A true RU97112090A (en) 1999-06-10
RU2176138C2 RU2176138C2 (en) 2001-11-27

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Country Status (28)

Country Link
US (4) US6075030A (en)
EP (4) EP0910948B1 (en)
JP (1) JP3852947B2 (en)
KR (1) KR100402523B1 (en)
CN (2) CN1079638C (en)
AR (2) AR001061A1 (en)
AT (4) ATE193182T1 (en)
AU (1) AU689684B2 (en)
BG (1) BG63375B1 (en)
BR (1) BR9510048A (en)
CA (1) CA2208141C (en)
CZ (1) CZ288779B6 (en)
DE (5) DE4444911A1 (en)
DK (4) DK0910948T3 (en)
ES (4) ES2166127T3 (en)
GR (1) GR3033502T3 (en)
HU (1) HU222565B1 (en)
IL (1) IL116332A (en)
MX (1) MX9704393A (en)
NZ (1) NZ297444A (en)
PL (2) PL183263B1 (en)
PT (4) PT910948E (en)
RU (1) RU2176138C2 (en)
SK (1) SK282838B6 (en)
TW (1) TW345488B (en)
UA (1) UA39986C2 (en)
WO (1) WO1996018299A1 (en)
ZA (1) ZA9510682B (en)

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AU765004B2 (en) * 1997-05-15 2003-09-04 Syngenta Participations Ag Fungicidal combinations comprising a 4-phenoxyquinoline
GB9718366D0 (en) 1997-08-29 1997-11-05 Ciba Geigy Ag Novel combinations
US6489348B1 (en) * 1997-12-18 2002-12-03 Basf Aktiengesellschaft Fungicidal mixtures based on amide compounds and pyridine derivatives
TW464471B (en) * 1997-12-18 2001-11-21 Basf Ag Fungicidal mixtures based on amide compounds and pyridine derivatives
DE19939841A1 (en) * 1998-11-20 2000-05-25 Bayer Ag Synergistic fungicide combination for use in plant protection contains 4,6-diphenoxy-5-halo-pyrimidine derivative and e.g. tebuconazole, fenpropimorph, azoxystrobin, carbendazim or folpet
UA72490C2 (en) * 1998-12-22 2005-03-15 Басф Акцієнгезелльшафт Fungicidal mixture and a method of controlling phytopathogenic fungi
NZ516198A (en) * 1999-05-24 2004-01-30 Lonza Ag Azole/amide oxide wood preservatives
DE19933938A1 (en) 1999-07-20 2001-01-25 Bayer Ag Fungicidal active ingredient combinations
US6649566B2 (en) 2001-12-13 2003-11-18 Morse Enterprises Limited, Inc. Stabilized concentrated formulations for enhancing plant defensive responses
AU2003257666A1 (en) 2002-08-23 2004-03-11 Kirin Beer Kabushiki Kaisha COMPOUND HAVING TGFss INHIBITORY ACTIVITY AND MEDICINAL COMPOSITION CONTAINING THE SAME
NZ546829A (en) * 2003-11-26 2009-12-24 Syngenta Participations Ag Method for controlling fungi and mites in textile substrates
PE20060801A1 (en) * 2004-12-23 2006-10-03 Basf Ag FUNGICIDE MIXTURES
WO2007002120A2 (en) * 2005-06-23 2007-01-04 Duke University Fungicidal effect by regulating signal transduction pathways
CN102349514A (en) * 2011-10-11 2012-02-15 海利尔药业集团股份有限公司 Bupirimate-containing antibacterial composition

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US4705800A (en) * 1985-06-21 1987-11-10 Ciba-Geigy Corporation Difluorbenzodioxyl cyanopyrrole microbicidal compositions
DE3623921A1 (en) * 1986-07-16 1988-01-21 Basf Ag OXIMETHER AND FUNGICIDES CONTAINING THEM
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