Fungicide mixture 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
WO9841094 A1 1998-09-24 [WO9841094] / 1998-09-24
申请号/申请日
1998WO-EP01034 / 1998-02-23
发明人
WAGNER OLIVER;BAYER HERBERT;MISSLITZ ULF;SCHIRMER ULRICH;AMMERMANN EBERHARD;LORENZ GISELA;STRATHMANN SIEGFRIED;
申请人
BASF;
主分类号
IPC分类号
A01N-037/50A01N-043/54A01N-047/24A01N-047/34
摘要
(WO9841094) The invention relates to a fungicide mixture with synergistic effect, containing a) a fungicide active compound of formula IA or IB wherein <u>- - -</u> represents a single or double bond and the index and substituents have the following meanings: R' -C[CO2CH3] =CHOCH3, -C[CO2CH3] =NOCH3, -C[CONHCH3] =NOCH3, -C[CO2CH3] =CHCH3, -C[CO2CH3] =CHCH2CH3, -C[COCH3] =NOCH3, -C[COCH2CH3] =NOCH3, -N(OCH3) -CO2CH3, -N(CH3) -CO2CH3, -N(CH2CH3) -CO2CH3; R'' a C-organic radical which is bonded directly or via an oxy-, mercapto-, amino- or alkylamino group; together with a group X and the ring Q or T to which they are bonded, an optionally substituted bicyclic, partially or completely unsaturated system; R<x> -OC[CO2CH3] =CHOCH3, -OC[CO2CH3] =CHCH3, -OC[CO2CH3] =CHCH2CH3, -SC[CO2CH3] =CHOCH3, -SC[CO2CH3] =CHCH3, -SC[CO2CH3] =CHCH2CH3, -N(CH3)C[CO2CH3] =CHOCH3, -N(CH3)C[CO2CH3] =NOCH3, -CH2C[CO2CH3] =CHOCH3, -CH2C[CO2CH3] =NOCH3, -CH2C[CONHCH3] =NOCH3; R<y> oxygen, sulfur, =CH- or =N-; n 0, 1, 2 or 3; X cyano, nitro, halogen, alkyl, halogenalkyl, alkoxy, halogenalkoxy, alkylthio; if n>1, an optionally substituted alkylene, alkenylene, oxyalkylene, oxyalkylenoxy, oxyalkenylene, oxyalkenylenoxy or butadiendiyl group bonded to two adjoining C-atoms of the phenyl ring; Y C- or -N-; Q cyclopentenyl, cyclohexenyl, phenyl, pyrrolyl, thienyl, furyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, thiadiazolyl, triazolyl, pyridinyl, 2-pyridonyl, pyrimidinyl and triazinyl; T phenyl, oxazolyl, thiazolyl, thiadiazolyl, oxadiazolyl, pyridinyl, pyrimidinyl and triazinyl, and b) the herbicide active agent II and/or b2) the herbicide active agent III.  The invention also relates to methods for producing mixtures of that type and the use of such mixtures for combatting harmful fungi in the area of plant and material protection.
机翻摘要
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地址
代理人
代理机构
;
优先权号
1997DE-1010760 1997-03-14
主权利要求
(WO9841094) Claims 1. Fungicidal mixture, comprising A) a fungicidally active compound of the formula IA or IB ^ - ^ is a single - or in which double bond and the index and the substituents have the following meaning: R′ - C [C0CH3]=CHOCH3, - C [C02CH3]=N0CH3, - C [CONHCH3]=NOR3, - C [C02CH3]=CHCH3, - C [C02CH3]=CHCH2CH3, - C [COCH3]=NOR3, - C [COCH2CH3]=NOR3, - N (OCH3) - C02CH3, - N (CH3) - C02CH3, - N (CH2CH3) - C02CH3; R " a C-organic radical, which is directly or indirectly or via an Oxy -, Mercapto -, amino -, or alkyl amino group is bonded; together with a group X and the ring Q or T, to which they are attached, an optionally substituted - bicyclithen an, - Sy stem partially or fully unsaturated, which in addition to carbon ring members of the group consisting of oxygen atoms, sulfur and nitrogen can; Rx- OC [C02CH3]=CH0CH3, - OC [C02CH3]=CHCH3, - OC [C02CH3]=CHCH2CH3, - SC [C02CH3]=CH0CH3, - SC [C02CH3]=CHCH3, - SC [C0 CH3]=CHCH2CH3, - N (CH3) C [C0 CH3]=CHOCH3, - N (CH3) C [C02CH3]=NOR3, - CH2C [CO2CH3]=CHOCH3, - CH2C [C02CH3]=NOR3, - CH2C [CONHCH3]=NOR3; Ryoxygen, sulfur, or - N - CH==; n is 0, 1, 2 or 3, wherein the radicals X may be different, when n is greater than 1; X cyano, Nitro, halogen, Cι-C4- alkyl, Cι-C4halogen - alkyl -, ~C C ι4- alkoxy, Cι-C4- haloalkoxy, Cχ-C4- Alkylthio; in the case, that n&amp;gt; is 1, two adjacent C atoms of the phenyl ring at a C-bonded3- C5- alkylene -, C3- C5- alkenylene -, - C-Oxy-C4- alkylene -, - Oxy-Cχ-C - alkylenoxy, Oxy-C2- C4alkynyleneeachc - -, Oxy-C2- C4- alkenylenoxy - diyl group or butadiene, where - in this chain may carry one to three of the following radicals in turn: halogen, C ι.- C4- alkyl, Cι-C4- haloalkyl, Cι-C4- alkoxy, Cι-C4Cι-C - - haloalkoxy or Alkylthio, Y=C - or - N -; Q Cyclopentenyl, Cyclohexenyl, phenyl, Pyrrolyl, Thienyl, Furyl, Pyrazolyl, Imidazolyl, Oxazolyl, Isoxazolyl, Thiazolyl, Thiadiazolyl, Triazolyl, Pyridinyl, 2- Pyridonyl, Pyrimidinyl and Triazinyl; T is phenyl, Oxazolyl, thiazolyl, thiadiazolyl, Oxa¬diazolyl, Pyridinyl, Pyrimidinyl and triazinyl, as well as bl) the herbicidally active compound II  and/or b2) the herbicidally active compound III in a synergistically effective amount. 2. Fungicidal mixture according to claim 1, characterized in, that the weight ratio of the compounds IA or IB to the compound II or 10:1 to 0.1: 1 and the weight ratio of the compounds IA or IB to the compound II and compound iii 10:1:0, 4 to 0.1: 1: 0.4 is. 3. Method for controlling harmful fungi, characterized in characterized -, in that the harmful fungi, their habitat or the plants to be kept free from them, seeds, soils, areas, materials or spaces with a compound of formula IA or IB according to claim 1 and the compound of formula II according to claim 1 and/or the compound iii according to claim 1 treated. 4. Method according to claim 3, characterized in, that the compound IA or IB according to claim 1 and the compound II according to claim 1 and/or the compound iii - dimensional claim 1 n_ge simultaneously, or in common n_ge¬separates, or sequentially dispenses. 5. Method for protecting crop plants from fungi according to claim 3, characterized in, that - the harmful fungi, their habitat or the plants to be kept free from them, seed or soils with 0.01 to 1 kg/ha of a compound IA or IB according to claim 1 treated. 6. Method according to claim 5, characterized in, that the compound II according to claim 1 in an amount of from 0.01 to 1 kg/ha applies. 7. Method according to claim 5, characterized in, that the compound III according to claim 1 in an amount of from 0.001 to 0.3 kg/ha applies. 8. Method for the protection of materials or spaces in front of fungi according to claim 3, characterized in, that the materials or spaces to be kept free from fungi with 0.01 to 20 gms/m3of a compound IA or IB according to claim 1 treated. 9. Method according to claim 8, characterized in, that the compound II according to claim 1 in an amount of from 0.01 to 20 gms/m3applies. 10. Method according to claim 8, characterized in, that the compound III according to claim 1 in an amount of from 0.01 to 20 gms/m3applies. 11. Use of a compound IA or IB according to claim 1 for the production of a fungicidally active synergistic mixture according to claim 1. 12. Use of the compound II according to claim 1 for the production of a fungicidally effective synergistic mixture according to claim 1. 13. Use of the compound III according to claim 1 reconverter a fungicidally effective synergistic mixture for manufacturing - according to claim 1.
法律状态
(WO9841094) LEGAL DETAILS FOR WO9841094  Actual or expected expiration date=2000-09-14    Legal state=DEAD    Status=LAPSED     Event publication date=1998-02-23  Event code=WO/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=WO WOEP9801034  Application date=1998-02-23  Standardized application number=1998WO-EP01034     Event publication date=1998-09-24  Event code=WO/A1  Event type=Examination events  Published application with search report  Publication country=WO  Publication number=WO9841094  Publication stage Code=A1  Publication date=1998-09-24  Standardized publication number=WO9841094     Event publication date=1998-09-24  Event code=WO/AL  Event indicator=Pos  Event type=Designated states  Designated countries for regional patents AM AZ BY KG KZ MD RU TJ TM AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE    Event publication date=1998-09-24  Event code=WO/AK  Event indicator=Pos  Event type=Designated states  Designated states AL AU BG BR BY CA CN CZ GE HU ID IL JP KR KZ LT LV MX NO NZ PL RO RU SG SI SK TR UA US    Event publication date=1998-10-22  Event code=WO/DFPE  Event type=Examination events  Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)    Event publication date=2000-09-14  Event code=WO/EETL  Event type=Event indicating Not In Force  PCT Application validity period expired. LEGAL DETAILS FOR DESIGNATED STATE AU6724098  Actual or expected expiration date=2003-10-12    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=AU Corresponding appl: AU6724098  Application date in the designated or member state=1998-02-23   Application number in the designated or member state=1998AU-0067240 Corresponding cc:  Designated or member state=AU Corresponding pat: AU6724098  Publication stage code in the designated or member state=A  Publication date in the designated or member state=1998-10-12   Publication number in the designated or member state=AU9867240    Event publication date=1998-10-12  Event code=AU/STCHG  Patent Status changed by the national office Corresponding cc:  Designated or member state=AU  LEGAL DETAILS FOR DESIGNATED STATE CA  Actual or expected expiration date=2000-09-14    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CA     Event publication date=2000-09-14  Event code=WO/NENP  Event type=Event indicating Not In Force  Non-entry into the national phase in: Corresponding cc:  Designated or member state=CA  LEGAL DETAILS FOR DESIGNATED STATE JP  Actual or expected expiration date=2000-03-03    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=JP Corresponding appl: JP1998540064    Event publication date=2000-03-03  Event code=WO/NENP  Event type=Event indicating Not In Force  Non-entry into the national phase in: Corresponding cc:  Designated or member state=JP
专利类型码
A1
国别省市代码
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