DD259343A5 - Fungizide zusammensetzungen - Google Patents
Fungizide zusammensetzungen Download PDFInfo
- Publication number
- DD259343A5 DD259343A5 DD87300230A DD30023087A DD259343A5 DD 259343 A5 DD259343 A5 DD 259343A5 DD 87300230 A DD87300230 A DD 87300230A DD 30023087 A DD30023087 A DD 30023087A DD 259343 A5 DD259343 A5 DD 259343A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- group
- atom
- optionally substituted
- chlorine atom
- plants
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 31
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- 239000004480 active ingredient Substances 0.000 claims abstract description 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 125000005843 halogen group Chemical group 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
- 239000000417 fungicide Substances 0.000 claims abstract description 4
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 4
- 239000000460 chlorine Substances 0.000 claims description 23
- 229910052801 chlorine Inorganic materials 0.000 claims description 18
- -1 cyano, methoxy Chemical group 0.000 claims description 18
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 10
- 239000011737 fluorine Substances 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 239000000969 carrier Substances 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 206010061217 Infestation Diseases 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
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- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 3
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- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims description 3
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
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- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
- 241000233866 Fungi Species 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- USYCQABRSUEURP-UHFFFAOYSA-N 1h-benzo[f]benzimidazole Chemical compound C1=CC=C2C=C(NC=N3)C3=CC2=C1 USYCQABRSUEURP-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
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- 239000004606 Fillers/Extenders Substances 0.000 description 1
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- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 244000141359 Malus pumila Species 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
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- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
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- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
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- 150000003871 sulfonates Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Photoreceptors In Electrophotography (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB868605032A GB8605032D0 (en) | 1986-02-28 | 1986-02-28 | Fungicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD259343A5 true DD259343A5 (de) | 1988-08-24 |
Family
ID=10593870
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD87300230A DD259343A5 (de) | 1986-02-28 | 1987-02-26 | Fungizide zusammensetzungen |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0240047B1 (fr) |
| JP (1) | JPS62207260A (fr) |
| CN (1) | CN87101634A (fr) |
| AT (1) | ATE59640T1 (fr) |
| AU (1) | AU592412B2 (fr) |
| BR (1) | BR8700908A (fr) |
| DD (1) | DD259343A5 (fr) |
| DE (1) | DE3766863D1 (fr) |
| ES (1) | ES2019617B3 (fr) |
| GB (1) | GB8605032D0 (fr) |
| GR (1) | GR3001491T3 (fr) |
| HU (1) | HU200890B (fr) |
| IE (1) | IE60075B1 (fr) |
| NZ (1) | NZ219422A (fr) |
| PL (1) | PL150452B1 (fr) |
| PT (1) | PT84367B (fr) |
| ZA (1) | ZA871391B (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5789431A (en) * | 1996-02-16 | 1998-08-04 | The University Of North Carolina At Chapel Hill | Naphthoquinone antitumor compound and method |
| WO2018093957A1 (fr) * | 2016-11-15 | 2018-05-24 | Bioelectron Technology Corporation | Composés amino-naphth [1,2-d] imidazol-5-one substitués en position 2 ou leurs sels pharmaceutiquement acceptables |
| JP2018083799A (ja) | 2016-11-15 | 2018-05-31 | バイオエレクトロン テクノロジー コーポレイション | 2−置換アミノ−ナフト[1,2−d]イミダゾール−5−オン化合物またはその製薬学上許容される塩 |
| CN116082264B (zh) * | 2021-10-29 | 2025-06-17 | 北京夏禾科技有限公司 | 一种有机电致发光材料及其器件 |
-
1986
- 1986-02-28 GB GB868605032A patent/GB8605032D0/en active Pending
-
1987
- 1987-02-26 NZ NZ219422A patent/NZ219422A/en unknown
- 1987-02-26 DD DD87300230A patent/DD259343A5/de not_active IP Right Cessation
- 1987-02-26 ZA ZA871391A patent/ZA871391B/xx unknown
- 1987-02-26 PL PL1987264320A patent/PL150452B1/pl unknown
- 1987-02-26 IE IE50287A patent/IE60075B1/en not_active IP Right Cessation
- 1987-02-26 DE DE8787200351T patent/DE3766863D1/de not_active Expired - Lifetime
- 1987-02-26 AT AT87200351T patent/ATE59640T1/de not_active IP Right Cessation
- 1987-02-26 EP EP87200351A patent/EP0240047B1/fr not_active Expired - Lifetime
- 1987-02-26 ES ES87200351T patent/ES2019617B3/es not_active Expired - Lifetime
- 1987-02-26 HU HU87756A patent/HU200890B/hu not_active IP Right Cessation
- 1987-02-26 CN CN198787101634A patent/CN87101634A/zh active Pending
- 1987-02-26 JP JP62041609A patent/JPS62207260A/ja active Pending
- 1987-02-26 AU AU69294/87A patent/AU592412B2/en not_active Ceased
- 1987-02-26 BR BR8700908A patent/BR8700908A/pt not_active Application Discontinuation
- 1987-02-26 PT PT84367A patent/PT84367B/pt not_active IP Right Cessation
-
1991
- 1991-02-21 GR GR91400209T patent/GR3001491T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IE60075B1 (en) | 1994-06-01 |
| PT84367B (pt) | 1989-10-04 |
| IE870502L (en) | 1987-08-28 |
| ZA871391B (en) | 1987-09-30 |
| BR8700908A (pt) | 1987-12-15 |
| AU6929487A (en) | 1987-09-03 |
| GB8605032D0 (en) | 1986-04-09 |
| PL150452B1 (en) | 1990-05-31 |
| CN87101634A (zh) | 1987-09-30 |
| AU592412B2 (en) | 1990-01-11 |
| DE3766863D1 (de) | 1991-02-07 |
| ATE59640T1 (de) | 1991-01-15 |
| NZ219422A (en) | 1989-04-26 |
| EP0240047A1 (fr) | 1987-10-07 |
| ES2019617B3 (es) | 1991-07-01 |
| JPS62207260A (ja) | 1987-09-11 |
| GR3001491T3 (en) | 1992-10-08 |
| PT84367A (en) | 1987-03-01 |
| EP0240047B1 (fr) | 1991-01-02 |
| PL264320A1 (en) | 1988-07-21 |
| HU200890B (en) | 1990-09-28 |
| HUT43930A (en) | 1988-01-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |