SU667101A3 - Фунгицидна композици - Google Patents
Фунгицидна композициInfo
- Publication number
- SU667101A3 SU667101A3 SU772553299A SU2553299A SU667101A3 SU 667101 A3 SU667101 A3 SU 667101A3 SU 772553299 A SU772553299 A SU 772553299A SU 2553299 A SU2553299 A SU 2553299A SU 667101 A3 SU667101 A3 SU 667101A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- tert
- fungicide
- butylphenyl
- torr
- leaves
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title description 3
- 239000000417 fungicide Substances 0.000 title description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- HNVIQLPOGUDBSU-WDSKDSINSA-N (2s,6s)-2,6-dimethylmorpholine Chemical compound C[C@H]1CNC[C@H](C)O1 HNVIQLPOGUDBSU-WDSKDSINSA-N 0.000 description 1
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000540505 Puccinia dispersa f. sp. tritici Species 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 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
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
- C07D295/03—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to acyclic carbon atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
(54) ФУНГИЦИДНАЯ КОМПОЗИЦИЯ 612 г 3-третбутил})енил-2-метилпропанал . Конденсаци происходи при сильном вьщелении СОд. По завершений реакции смесь еще 2 час переМбшивают при температуре . « После этого при пониженной давлении отгон ют избыточную муравьиную кислоту, отделение муравьиной кислоты в большой мере происходит в вахкуме водоструйного масоса п . Щ вшепеан Ьс11О8анй из Формйата добавл ют по капл м 506 г 40%-него водного pacTBifspa Шдкдзго натра. При температур должна быть 80-100 с, что способстауетТхо potdeMy смешению обрезуНощейс шино вой фазы с мелочной. Дл сн)жёШй в зкбсти добавл ют 200 г . Органическую фазу по отделении weлочной фазы Два даы пррмЬааават 250 г ВСЙЯЫ -: г .---.- Vi :;:-:: -/-. ДЛЯ дальнейшей очистки ами пере гон ют при торр е. пё гонйой колонне с п тью тарелками по фракци м . Помимо небольшого головного погона (до i 43 С/О/2 мм рт.ст. 5 О г получают 865 г (третбутилфенил-2-ме тил-1 -прртил) -2,6 -цис-диметйдабрфо лийа, ЭТО количество перегон етс при давлении 0,2 мм рт.ст. и темпе ратуре 143-1 46 С. Согласно газох ро матографическому анализу амин содер жит cBtfiie 98% чистого вев1ёства.. В Пересчете На альдегид выход состав л ет 84,5%. .,;,. 14 Пример 2. Синтез (З-п-третбутилфенил-2-мвтил-1-пропил )-2,6-транс-дю етидморфолина . К .70 г 98%-ной муравьиной кислоты, охлаждаемой льдом, добавл ют 29 г 2,6-транс-диметилморфолина. Затем, переманива , добавл ют 41 г 3-г1-третбутилфенил-2-метилпропанал . Реакционну смесь б час нагревают до 100 С. В начале реакции взаимодействий набЛкдаетс сильное вьщеление СО , заметно уменьшанвдеес по истеЧёнии приблизительно 1 час. Дальнейшую об рабдтк у провод т аналогично Примеру 1-.--, При Давлении 5 мм.рт.ст. и темпеP Tyjpe 168-169 0 (З-д-третбутилфенйл-2-ме Ил-1-пропил )-2,6-трансДГО етигалорфолин перегон етс . Выход составЛ е 52 г (86% в пересчете на йльдегвд). 11 г амина раствор ют в 20 г этилацетата, насыаенног® сух«м хлористым водородом, при охлаждении вькристаллизовываетс гидрохлорвд (его. т.пл. IfiSC) . Аналогичным способом получают слёдунхцие соединени формуты ,
ДеЛзтвуюиее начало
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Изобретение иллюстрируетс слёЦ дующими примерами...
На листь х выращенных Sвегетационных сосудах ростков пшеницы сорта юбил р напыл ют врДНые эмульсии (80 вес.% дёйствукюегр начала и 20 вес..% эмульгатора), после присыхани напыленного слой; нанос т споры мучнистой росы зла ков & f5i| tmiitit5 vaz trttici ) .ИспыTy iae растени затем помацают и парниковые услови при 20-22с и 75-80%-ной относительной влажности воздуха. Через 10 дней определ ют степень развити мучнистой
росы. ..- ;:.,.: -
т.пл.
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-.
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Листь выращенных в горьках ростков чмен сорта Tlrtbecks Vnton обрабатывают водньми действующими
Листь выращенных в вегетационjHbK сосудах растений пшеницы заражают спорами бурой ржавчинй пшеницы (Pucciftio rsuondila ) искусственньм способом и помещают на 48 час в наоыщениую вод ным паром камеру при 20-25 С. После этого на растеHiffi напыл ют водные растворы, содержащие 1ВО% испытуемого дохимиката и 20% натрийлигнинсульфоната, и по метают в парниковые услови при 2022°С и относительной влажности воздуха 75-80%. Через 10 дней производ т оценку степени развити ржавчинного гриба.,
Поражение листьев после напылени х%-ного раствора дохимиката
,025
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, предложенные соединени обладают высоким фунгицид; ным деЙст||Йем.
Claims (2)
1. ВшШе а за вка ФРГ 12144 кл. 45 t 9/22, 1966.
2.Выложенна за вка ФРГ 246151 кл. С 071) 295/02, 07.1976.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MD95-0017A MD323C2 (ru) | 1976-12-15 | 1994-12-13 | Фунгицидная композиция |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2656747A DE2656747C2 (de) | 1976-12-15 | 1976-12-15 | Morpholinderivate |
| NO781229A NO146026C (no) | 1976-12-15 | 1978-04-07 | Pesticide morfolinderivater |
| FI781117A FI67379C (fi) | 1976-12-15 | 1978-04-12 | Saosom fungisider anvaendbara morfolinderivat |
| AU35565/78A AU3556578A (en) | 1976-12-15 | 1978-04-28 | Morpholine derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU667101A3 true SU667101A3 (ru) | 1979-06-05 |
Family
ID=36763781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU772553299A SU667101A3 (ru) | 1976-12-15 | 1977-12-14 | Фунгицидна композици |
Country Status (28)
| Country | Link |
|---|---|
| JP (1) | JPS5377070A (ru) |
| AT (1) | AT356455B (ru) |
| AU (1) | AU3556578A (ru) |
| BE (1) | BE861828A (ru) |
| BR (1) | BR7708252A (ru) |
| CA (1) | CA1086734A (ru) |
| CH (1) | CH635729A5 (ru) |
| CS (1) | CS195346B2 (ru) |
| DD (1) | DD134040A5 (ru) |
| DE (1) | DE2656747C2 (ru) |
| DK (1) | DK145625C (ru) |
| FI (1) | FI67379C (ru) |
| FR (1) | FR2374315A1 (ru) |
| GB (1) | GB1591267A (ru) |
| HU (1) | HU178175B (ru) |
| IN (1) | IN149397B (ru) |
| IT (1) | IT1092170B (ru) |
| KE (1) | KE3165A (ru) |
| LU (1) | LU79385A1 (ru) |
| MY (1) | MY8500333A (ru) |
| NL (1) | NL190012C (ru) |
| NO (1) | NO146026C (ru) |
| NZ (1) | NZ185971A (ru) |
| OA (1) | OA05971A (ru) |
| PL (1) | PL106524B1 (ru) |
| SE (1) | SE441527B (ru) |
| SU (1) | SU667101A3 (ru) |
| YU (1) | YU40701B (ru) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA024384B1 (ru) * | 2013-06-27 | 2016-09-30 | Институт Нефтехимических Процессов Им. Академика Ю. Мамедалиева, Нан Азербайджана | Применение комплексной соли 2-морфолилметил-5-метилфенола в качестве пестицида против оидиума в плодах и листьях винограда |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT354187B (de) | 1976-11-22 | 1979-12-27 | Hoffmann La Roche | Fungizides mittel |
| DE2727482A1 (de) * | 1977-06-18 | 1979-01-11 | Basf Ag | Derivate cyclischer amine |
| DE2822326A1 (de) * | 1978-05-22 | 1979-11-29 | Basf Ag | Antimykotische mittel |
| DE2830127A1 (de) | 1978-07-08 | 1980-01-17 | Basf Ag | N-arylpropyl-substituierte cyclische amine |
| DE2830120A1 (de) | 1978-07-08 | 1980-01-17 | Basf Ag | Substituierte phenylpropylhalogenide |
| DE2830999A1 (de) * | 1978-07-14 | 1980-01-31 | Basf Ag | Verfahren zur herstellung von stereoisomeren n-aralkyl-2,6-dimethylmorpholinen |
| DE2907614A1 (de) * | 1979-02-27 | 1980-09-04 | Basf Ag | Optische aktive formen des 1- eckige klammer auf 3-(p-tert.-buthylphenyl)-2- methylpropyl eckige klammer zu -cis-3,5- dimethylmorpholins |
| US4283534A (en) | 1979-04-11 | 1981-08-11 | Basf Aktiengesellschaft | Reductive alkylation of nitrogen heterocycles |
| CH644113A5 (en) * | 1979-08-17 | 1984-07-13 | Hoffmann La Roche | N-substituted 2,6-dimethylmorpholine compounds |
| IT1220970B (it) * | 1979-08-17 | 1990-06-21 | Hoffmann La Roche | Composti eteterociclici ad azione fungicida particolare per la lotta contro la candida albicans |
| DE2935452A1 (de) * | 1979-09-01 | 1981-03-19 | Basf Ag, 6700 Ludwigshafen | N-phenylpropylsubstituierte azole, verfahren zu ihrer herstellung und diese enthaltende fungizide |
| DE3001303A1 (de) | 1980-01-16 | 1981-07-23 | Basf Ag, 6700 Ludwigshafen | Optisch aktive phenylpropan-derivate, ihre herstellung und verwendung |
| DE3121349A1 (de) * | 1981-05-29 | 1982-12-16 | Basf Ag, 6700 Ludwigshafen | Cyclohexenderivate, verfahren zu ihrer herstellung und diese enthaltende fungizide |
| DE3261377D1 (en) * | 1981-07-31 | 1985-01-10 | Fbc Ltd | Fungicidal composition containing prochloraz |
| DE3263407D1 (en) * | 1981-08-29 | 1985-06-05 | Basf Ag | Fungicides containing phenylpropylammonium salt, and process for combating fungi |
| DE3217964A1 (de) * | 1982-05-13 | 1983-11-17 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von cis-2-,6-dimethylmorpholin |
| DE3321712A1 (de) * | 1983-06-16 | 1984-12-20 | Basf Ag, 6700 Ludwigshafen | 2,6-trans-dimethylmorpholinderivate und diese enthaltende fungizide und verfahren zur bekaempfung von pilzen |
| DE3582728D1 (de) * | 1985-01-17 | 1991-06-06 | Ici Plc | Tertiaere aminoverbindungen. |
| DE3539412A1 (de) * | 1985-11-07 | 1987-05-14 | Basf Ag | Holzschutzmittel |
| GB2192881A (en) * | 1986-07-16 | 1988-01-27 | Ici Plc | Tertiary amine compounds |
| DE3627071A1 (de) * | 1986-08-09 | 1988-02-11 | Bayer Ag | Substituierte hydroxypropylamin-derivate |
| FI874121A7 (fi) * | 1986-09-24 | 1988-03-25 | Sumitomo Chemical Co | Heterocykliska foereningar, och deras framstaellning och anvaendning. |
| DE3633520A1 (de) * | 1986-10-02 | 1988-04-14 | Huels Chemische Werke Ag | Verfahren zur herstellung von n-substituierten morpholin- und piperidin-derivaten |
| DE3711345A1 (de) * | 1987-04-03 | 1988-10-20 | Bayer Ag | Substituierte propylamine |
| US5135955A (en) * | 1988-04-25 | 1992-08-04 | Eli Lilly And Company | Propanamine derivatives |
| DE3902509A1 (de) * | 1989-01-28 | 1990-08-09 | Basf Ag | Fungizide mischung |
| DE3918978A1 (de) * | 1989-06-10 | 1990-12-13 | Wolman Gmbh Dr | Mischung fuer den holzschutz |
| IT1240427B (it) * | 1990-03-02 | 1993-12-15 | Ministero Dall Uni E Della Ric | Arilpropilammine ad azione antifungina |
| DE4124255A1 (de) * | 1991-07-22 | 1993-01-28 | Basf Ag | Fungizide mischung |
| DE4309856A1 (de) * | 1993-03-26 | 1994-09-29 | Basf Ag | Fungizide Mischung |
| IT1276165B1 (it) | 1995-11-24 | 1997-10-27 | Caffaro Spa Ind Chim | Procedimento per la sintesi enantioselettiva di derivati chirali di s-3-(4'-tert-butil)-fenil-2-metil propilammina, fungicidi sistemici |
| DE19834028A1 (de) | 1998-07-28 | 2000-02-03 | Wolman Gmbh Dr | Verfahren zur Behandlung von Holz gegen den Befall durch holzschädigende Pilze |
| DE10347090A1 (de) | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE10349501A1 (de) | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE102004049761A1 (de) | 2004-10-12 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| WO2007000628A1 (en) * | 2005-01-07 | 2007-01-04 | Ranbaxy Laboratories Limited | Intermediate of amorolfine or its salt |
| DE102005015677A1 (de) | 2005-04-06 | 2006-10-12 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| CN104170838B (zh) | 2005-06-09 | 2016-03-30 | 拜尔农作物科学股份公司 | 活性物质结合物 |
| DE102005026482A1 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| EP1749826A1 (en) | 2005-07-28 | 2007-02-07 | Galderma S.A. | Process of producing bepromoline |
| CN100391951C (zh) * | 2006-03-30 | 2008-06-04 | 江苏飞翔化工股份有限公司 | 一种丁苯吗啉的合成方法 |
| DE102006023263A1 (de) | 2006-05-18 | 2007-11-22 | Bayer Cropscience Ag | Synergistische Wirkstoffkombinationen |
| DE102007045920B4 (de) | 2007-09-26 | 2018-07-05 | Bayer Intellectual Property Gmbh | Synergistische Wirkstoffkombinationen |
| UA104887C2 (ru) | 2009-03-25 | 2014-03-25 | Баєр Кропсаєнс Аг | Синергические комбинации активных веществ |
| CN104430378A (zh) | 2009-07-16 | 2015-03-25 | 拜尔农作物科学股份公司 | 含苯基三唑的协同活性物质结合物 |
| EP3089985B1 (en) | 2014-01-03 | 2018-06-27 | Council of Scientific and Industrial Research | Silicon-based fungicides and process for producing the same |
| UA120628C2 (uk) | 2014-11-07 | 2020-01-10 | Басф Се | Пестицидні суміші |
| EP2910126A1 (en) | 2015-05-05 | 2015-08-26 | Bayer CropScience AG | Active compound combinations having insecticidal properties |
| WO2017157920A1 (en) | 2016-03-16 | 2017-09-21 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on fruits |
| EP3429357B1 (en) | 2016-03-16 | 2025-09-17 | Basf Se | Use of a specific tetrazolinone for combating resistant phytopathogenic fungi on cereals |
| US11241012B2 (en) | 2016-03-16 | 2022-02-08 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1179940B (de) * | 1959-05-05 | 1964-10-22 | Searle & Co | Verfahren zur Herstellung von 2-Phenyl-3-methyl-4-(1-methyl-2-phenylaethylamino)-morpholin |
| AT354187B (de) * | 1976-11-22 | 1979-12-27 | Hoffmann La Roche | Fungizides mittel |
-
1976
- 1976-12-15 DE DE2656747A patent/DE2656747C2/de not_active Expired
-
1977
- 1977-11-28 CA CA291,886A patent/CA1086734A/en not_active Expired
- 1977-12-09 NL NLAANVRAGE7713685,A patent/NL190012C/xx not_active IP Right Cessation
- 1977-12-12 JP JP14823877A patent/JPS5377070A/ja active Pending
- 1977-12-12 CS CS778307A patent/CS195346B2/cs unknown
- 1977-12-12 CH CH1530877A patent/CH635729A5/de not_active IP Right Cessation
- 1977-12-12 BR BR7708252A patent/BR7708252A/pt unknown
- 1977-12-13 HU HU77BA3607A patent/HU178175B/hu unknown
- 1977-12-13 DD DD77202589A patent/DD134040A5/xx unknown
- 1977-12-13 PL PL1977202897A patent/PL106524B1/pl unknown
- 1977-12-14 NZ NZ185971A patent/NZ185971A/xx unknown
- 1977-12-14 AT AT893177A patent/AT356455B/de not_active IP Right Cessation
- 1977-12-14 GB GB51961/77A patent/GB1591267A/en not_active Expired
- 1977-12-14 DK DK556577A patent/DK145625C/da not_active IP Right Cessation
- 1977-12-14 IT IT52207/77A patent/IT1092170B/it active
- 1977-12-14 BE BE183431A patent/BE861828A/xx not_active IP Right Cessation
- 1977-12-14 SU SU772553299A patent/SU667101A3/ru active
- 1977-12-15 FR FR7737918A patent/FR2374315A1/fr active Granted
-
1978
- 1978-04-06 YU YU827/78A patent/YU40701B/xx unknown
- 1978-04-06 LU LU79385A patent/LU79385A1/de unknown
- 1978-04-07 NO NO781229A patent/NO146026C/no unknown
- 1978-04-11 SE SE7804074A patent/SE441527B/sv not_active IP Right Cessation
- 1978-04-12 FI FI781117A patent/FI67379C/fi not_active IP Right Cessation
- 1978-04-28 AU AU35565/78A patent/AU3556578A/en active Pending
- 1978-05-09 IN IN499/CAL/78A patent/IN149397B/en unknown
- 1978-05-25 OA OA56510A patent/OA05971A/xx unknown
-
1981
- 1981-09-30 KE KE3165A patent/KE3165A/xx unknown
-
1985
- 1985-12-30 MY MY333/85A patent/MY8500333A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA024384B1 (ru) * | 2013-06-27 | 2016-09-30 | Институт Нефтехимических Процессов Им. Академика Ю. Мамедалиева, Нан Азербайджана | Применение комплексной соли 2-морфолилметил-5-метилфенола в качестве пестицида против оидиума в плодах и листьях винограда |
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