IL33254A - N-noble-P-dialkylaminophenyl-hydrazones, a process for their production and use as fungicides - Google Patents
N-noble-P-dialkylaminophenyl-hydrazones, a process for their production and use as fungicidesInfo
- Publication number
- IL33254A IL33254A IL6933254A IL3325469A IL33254A IL 33254 A IL33254 A IL 33254A IL 6933254 A IL6933254 A IL 6933254A IL 3325469 A IL3325469 A IL 3325469A IL 33254 A IL33254 A IL 33254A
- Authority
- IL
- Israel
- Prior art keywords
- compound
- active
- carbon atoms
- soil
- alkyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 9
- 238000002360 preparation method Methods 0.000 title description 5
- 239000000417 fungicide Substances 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 61
- 239000002689 soil Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 12
- 239000003085 diluting agent Substances 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 10
- 241000233866 Fungi Species 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 241000607479 Yersinia pestis Species 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 14
- -1 alkali metal salts Chemical class 0.000 description 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 206010061217 Infestation Diseases 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 241000918584 Pythium ultimum Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- 235000010582 Pisum sativum Nutrition 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 238000009924 canning Methods 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 150000007857 hydrazones Chemical class 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 241000223218 Fusarium Species 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
- 208000031888 Mycoses Diseases 0.000 description 1
- 241000222831 Phialophora <Chaetothyriales> Species 0.000 description 1
- 241000219843 Pisum Species 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 241000233626 Plasmopara Species 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241001361634 Rhizoctonia Species 0.000 description 1
- 241000865903 Thielaviopsis Species 0.000 description 1
- 241000722093 Tilletia caries Species 0.000 description 1
- 241000031845 Tilletia laevis Species 0.000 description 1
- GHVZOJONCUEWAV-UHFFFAOYSA-N [K].CCO Chemical compound [K].CCO GHVZOJONCUEWAV-UHFFFAOYSA-N 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical group O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 150000003948 formamides Chemical class 0.000 description 1
- 208000024386 fungal infectious disease Diseases 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000002464 fungitoxic effect Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 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
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681810581 DE1810581C3 (de) | 1968-11-23 | N-Acyl-p-dialkylamino-phenylhydrazone, Verfahren zu ihrer Herstellung und deren Verwendung zur Bekämpfung von phytopathogene Pilzen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL33254A0 IL33254A0 (en) | 1969-12-31 |
| IL33254A true IL33254A (en) | 1972-09-28 |
Family
ID=5714129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL6933254A IL33254A (en) | 1968-11-23 | 1969-10-27 | N-noble-P-dialkylaminophenyl-hydrazones, a process for their production and use as fungicides |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US3660410A (cs) |
| AT (1) | AT301258B (cs) |
| BE (1) | BE742047A (cs) |
| BG (1) | BG17446A3 (cs) |
| CH (1) | CH524573A (cs) |
| CS (1) | CS158257B2 (cs) |
| DK (1) | DK125128B (cs) |
| ES (1) | ES373806A1 (cs) |
| GB (1) | GB1273277A (cs) |
| IL (1) | IL33254A (cs) |
| NL (1) | NL6917030A (cs) |
| RO (1) | RO54696A (cs) |
| SE (1) | SE370936B (cs) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4447450A (en) * | 1982-03-25 | 1984-05-08 | Chevron Research Company | 2,2-Bis(haloalkenyl)-1-cyano-1-alkoxycarbonylethylene fungicides |
| US20120045522A1 (en) * | 2010-08-20 | 2012-02-23 | Dow Agrosciences Llc | Synergistic fungicidal and algicidal compositions including 7-hydroxy-indanone benzoylhydrazones and copper |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3060192A (en) * | 1959-04-29 | 1962-10-23 | Olin Mathieson | Production of enantiomers of alphamethyl-phenethyl hydrazine and intermediate |
-
1969
- 1969-10-22 CH CH1583969A patent/CH524573A/de not_active IP Right Cessation
- 1969-10-27 IL IL6933254A patent/IL33254A/en unknown
- 1969-11-04 DK DK582469AA patent/DK125128B/da unknown
- 1969-11-06 RO RO61481A patent/RO54696A/ro unknown
- 1969-11-06 BG BG013311A patent/BG17446A3/xx unknown
- 1969-11-07 GB GB54661/69A patent/GB1273277A/en not_active Expired
- 1969-11-12 NL NL6917030A patent/NL6917030A/xx unknown
- 1969-11-13 US US876589A patent/US3660410A/en not_active Expired - Lifetime
- 1969-11-19 CS CS762569A patent/CS158257B2/cs unknown
- 1969-11-21 AT AT1088569A patent/AT301258B/de not_active IP Right Cessation
- 1969-11-21 BE BE742047D patent/BE742047A/xx unknown
- 1969-11-22 ES ES373806A patent/ES373806A1/es not_active Expired
- 1969-11-24 SE SE6016126*3A patent/SE370936B/xx unknown
-
1972
- 1972-02-08 US US00224623A patent/US3760078A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| SE370936B (cs) | 1974-11-04 |
| RO54696A (cs) | 1973-04-12 |
| CS158257B2 (cs) | 1974-10-15 |
| DE1810581B2 (de) | 1977-05-05 |
| CH524573A (de) | 1972-06-30 |
| IL33254A0 (en) | 1969-12-31 |
| BG17446A3 (bg) | 1973-11-10 |
| BE742047A (cs) | 1970-05-21 |
| AT301258B (de) | 1972-08-25 |
| DE1810581A1 (de) | 1970-06-18 |
| US3760078A (en) | 1973-09-18 |
| US3660410A (en) | 1972-05-02 |
| DK125128B (da) | 1973-01-02 |
| GB1273277A (en) | 1972-05-03 |
| ES373806A1 (es) | 1972-02-16 |
| NL6917030A (cs) | 1970-05-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PL97786B1 (pl) | Srodek szkodnikobojczy i regulujacy wzrost roslin | |
| PL100147B1 (pl) | Srodek do usuwania lisci z roslin bawelny,jabloni,roslin hibiscus,winorosli wlasciwej i roz | |
| US3501578A (en) | Fungicidal composition containing phenyl - mercaptomethane-sulfonamide and method of using the same | |
| CA1199928A (en) | Pesticidal compositions | |
| JPS6252743B2 (cs) | ||
| US3518074A (en) | Benzoylcholine halides as plant growth stunting agents | |
| IL33254A (en) | N-noble-P-dialkylaminophenyl-hydrazones, a process for their production and use as fungicides | |
| EP0277091A2 (en) | 2-Imino-1,3-dithietanes, their preparation and use as pesticides | |
| US3819357A (en) | Quaternary thenyl ammonium salts as plant growth control agents | |
| DE2451588A1 (de) | Derivate des 1,2,4-oxadiazols, verfahren zu ihrer herstellung und ihre verwendung | |
| USRE29439E (en) | Certain 1,2,4-Oxa- and -thiadiazol-5-ylthioalkanoic acid derivatives | |
| CS232736B2 (en) | Fungicide agent and method of active component production | |
| US3956307A (en) | Benzimidazole-1-carboximidic acid esters | |
| US3658992A (en) | Sulfamide derivatives | |
| SU519109A3 (ru) | Фунгицидное средство | |
| SU849976A3 (ru) | Фунгицидоинсектицидное средство | |
| EP0007162B1 (en) | Novel n-substituted 2-oxo-3-benzothiazoline derivatives, their use as leguminous plant growth regulants, and plant growth regulating compositions containing said derivatives as the active ingredients | |
| US3609175A (en) | New substituted thiocarbamates | |
| CA1083169A (en) | Dialkylthiolophosphoryl urea pesticides | |
| US3748343A (en) | Quaternary thenyl ammonium salts | |
| CA1095927A (en) | Pesticidally active dialkylthiolophosphoryl-ureas | |
| CA1218363A (en) | Pesticidal nitromethylene derivatives | |
| KR800000222B1 (ko) | 1-페닐-1, 3, 5, 7,-테트라아자-4-설파-헵트-1-엔-6-온 유도체의 제조방법 | |
| KR810001153B1 (ko) | 사이클로프로판 카복실산 아닐리드류의 제조방법 | |
| CS196426B2 (en) | Agents for treatment of plants to influence growth and method of producing the active constituent |