CS214757B2 - Fungicide means and method of making the active substances - Google Patents
Fungicide means and method of making the active substances Download PDFInfo
- Publication number
- CS214757B2 CS214757B2 CS806402A CS640280A CS214757B2 CS 214757 B2 CS214757 B2 CS 214757B2 CS 806402 A CS806402 A CS 806402A CS 640280 A CS640280 A CS 640280A CS 214757 B2 CS214757 B2 CS 214757B2
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- Czechoslovakia
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- acid
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- 230000000855 fungicidal effect Effects 0.000 title claims description 5
- 239000013543 active substance Substances 0.000 title description 20
- 239000000417 fungicide Substances 0.000 title description 4
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims description 26
- 239000002253 acid Substances 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 20
- 239000004480 active ingredient Substances 0.000 claims description 14
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 239000011230 binding agent Substances 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000001401 1,2,4-triazol-4-yl group Chemical group N=1N=C([H])N([*])C=1[H] 0.000 claims description 2
- AJSLQYMVPFTISC-UHFFFAOYSA-N 1-(2h-triazol-4-yl)butan-2-ol Chemical class CCC(O)CC1=CNN=N1 AJSLQYMVPFTISC-UHFFFAOYSA-N 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 43
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- 241000196324 Embryophyta Species 0.000 description 30
- 239000002904 solvent Substances 0.000 description 26
- 206010061217 Infestation Diseases 0.000 description 25
- -1 1- (4-chlorophenoxy) -1- (1,2,4-triazolyl) -3,3-dimethyl-4-fluorobutan-2-ol Chemical compound 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
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- 239000000243 solution Substances 0.000 description 14
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- 241000221785 Erysiphales Species 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 11
- 230000001681 protective effect Effects 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
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- 230000000694 effects Effects 0.000 description 8
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- 235000011152 sodium sulphate Nutrition 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
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- 241001480061 Blumeria graminis Species 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
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- 239000003995 emulsifying agent Substances 0.000 description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
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- 239000000126 substance Substances 0.000 description 6
- 240000008067 Cucumis sativus Species 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
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- 150000007513 acids Chemical class 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
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- 239000007787 solid Substances 0.000 description 4
- FMTQEESQZPMFRD-UHFFFAOYSA-N 4-fluoro-3-(fluoromethyl)-3-methylbutan-2-one Chemical compound CC(=O)C(C)(CF)CF FMTQEESQZPMFRD-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 3
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 3
- 244000141359 Malus pumila Species 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 241001123569 Puccinia recondita Species 0.000 description 3
- 150000008065 acid anhydrides Chemical class 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- 235000013844 butane Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
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- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
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- WBLIXGSTEMXDSM-UHFFFAOYSA-N chloromethane Chemical compound Cl[CH2] WBLIXGSTEMXDSM-UHFFFAOYSA-N 0.000 description 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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- LLCOIQRNSJBFSN-UHFFFAOYSA-N methane;sulfurochloridic acid Chemical compound C.OS(Cl)(=O)=O LLCOIQRNSJBFSN-UHFFFAOYSA-N 0.000 description 1
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- GRRYSIXDUIAUGY-UHFFFAOYSA-N n-methylcarbamoyl chloride Chemical compound CNC(Cl)=O GRRYSIXDUIAUGY-UHFFFAOYSA-N 0.000 description 1
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- PJGSXYOJTGTZAV-UHFFFAOYSA-N pinacolone Chemical class CC(=O)C(C)(C)C PJGSXYOJTGTZAV-UHFFFAOYSA-N 0.000 description 1
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- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
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- 150000003460 sulfonic acids Chemical class 0.000 description 1
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- 229910052717 sulfur Inorganic materials 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical class OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- GIZSHQYTTBQKOQ-UHFFFAOYSA-N threo-Syringoylglycerol Chemical compound COC1=CC(C(O)C(O)CO)=CC(OC)=C1O GIZSHQYTTBQKOQ-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792938534 DE2938534A1 (de) | 1979-09-24 | 1979-09-24 | Acylierte triazolyl-(gamma)-fluorpinakolyl-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS214757B2 true CS214757B2 (en) | 1982-05-28 |
Family
ID=6081667
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS806402A CS214757B2 (en) | 1979-09-24 | 1980-09-22 | Fungicide means and method of making the active substances |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4359470A (ro) |
| EP (1) | EP0025949B1 (ro) |
| JP (1) | JPS5655379A (ro) |
| AR (1) | AR228744A1 (ro) |
| AT (1) | ATE4205T1 (ro) |
| AU (1) | AU537679B2 (ro) |
| BR (1) | BR8006076A (ro) |
| CA (1) | CA1189516A (ro) |
| CS (1) | CS214757B2 (ro) |
| DD (1) | DD153050A5 (ro) |
| DE (2) | DE2938534A1 (ro) |
| DK (1) | DK401180A (ro) |
| EG (1) | EG14311A (ro) |
| ES (1) | ES8106710A1 (ro) |
| FI (1) | FI66854C (ro) |
| GR (1) | GR70290B (ro) |
| HU (1) | HU186752B (ro) |
| IL (1) | IL61106A (ro) |
| NO (1) | NO802616L (ro) |
| NZ (1) | NZ195006A (ro) |
| PL (1) | PL124720B1 (ro) |
| PT (1) | PT71804B (ro) |
| RO (1) | RO80677A (ro) |
| TR (1) | TR20766A (ro) |
| ZA (1) | ZA805889B (ro) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2938575A1 (de) * | 1979-09-24 | 1981-04-23 | Bayer Ag, 5090 Leverkusen | Acylierte imidazolyl-(gamma)-fluorpinakolyl-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE3033592A1 (de) * | 1980-09-06 | 1982-04-22 | Bayer Ag, 5090 Leverkusen | Fluorierte 1-azolyl-butan-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| EP0095115A1 (de) * | 1982-05-26 | 1983-11-30 | Bayer Ag | Substituierte Diphenylether |
| US4610716A (en) * | 1982-12-14 | 1986-09-09 | Ciba-Geigy Corporation | Fluorinated azolyl ethanol growth regulators and microbicides |
| EP0116262B1 (de) * | 1983-01-10 | 1989-12-27 | Ciba-Geigy Ag | Fluorazolyl-propanol-Derivate als Mikrobizide und wuchsregulierende Mittel |
| GB8302500D0 (en) * | 1983-01-29 | 1983-03-02 | Pfizer Ltd | Antifungal agents |
| GB8305377D0 (en) * | 1983-02-25 | 1983-03-30 | Pfizer Ltd | Antifungal agents |
| JP2755869B2 (ja) * | 1992-06-11 | 1998-05-25 | 三洋電機株式会社 | 電気掃除機 |
| US6673346B1 (en) | 1999-08-31 | 2004-01-06 | The Regents Of The University Of Michigan | Compositions and methods for the treatment of sepsis |
| US7060442B2 (en) | 2000-10-30 | 2006-06-13 | Regents Of The University Of Michigan | Modulators on Nod2 signaling |
| US7582425B2 (en) | 2001-09-21 | 2009-09-01 | The Regents Of The University Of Michigan | Atlastin |
| US7108975B2 (en) | 2001-09-21 | 2006-09-19 | Regents Of The University Of Michigan | Atlastin |
| US7432057B2 (en) | 2004-01-30 | 2008-10-07 | Michigan State University | Genetic test for PSE-susceptible turkeys |
| EP2155910A4 (en) | 2007-05-08 | 2010-06-02 | Univ Duke | COMPOSITIONS AND METHODS FOR CHARACTERIZING AND REGULATING ODOR PERCEPTION |
| JP6507065B2 (ja) * | 2014-08-25 | 2019-04-24 | 住友化学株式会社 | 化合物、樹脂、レジスト組成物及びレジストパターンの製造方法 |
| CN111018851B (zh) * | 2019-12-17 | 2020-12-15 | 陕西科技大学 | 一种腐植酸控释三唑醇杀菌剂及其制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2811919A1 (de) * | 1978-03-18 | 1979-09-27 | Bayer Ag | Acylierte 1-azolyl-2-hydroxy-butan- derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE2811916A1 (de) * | 1978-03-18 | 1979-09-27 | Bayer Ag | Antimikrobielle mittel |
| DE2827968A1 (de) * | 1978-06-26 | 1980-01-10 | Bayer Ag | Sulfenylierte carbamoyl-triazolyl- o,n-acetale, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE2918896A1 (de) * | 1979-05-10 | 1980-11-20 | Bayer Ag | Antimikrobielle mittel |
-
1979
- 1979-09-24 DE DE19792938534 patent/DE2938534A1/de not_active Withdrawn
-
1980
- 1980-09-04 NO NO802616A patent/NO802616L/no unknown
- 1980-09-08 RO RO80102118A patent/RO80677A/ro unknown
- 1980-09-12 EP EP80105459A patent/EP0025949B1/de not_active Expired
- 1980-09-12 AT AT80105459T patent/ATE4205T1/de not_active IP Right Cessation
- 1980-09-12 DE DE8080105459T patent/DE3064292D1/de not_active Expired
- 1980-09-15 PT PT71804A patent/PT71804B/pt unknown
- 1980-09-17 US US06/187,866 patent/US4359470A/en not_active Expired - Lifetime
- 1980-09-22 CS CS806402A patent/CS214757B2/cs unknown
- 1980-09-22 FI FI802985A patent/FI66854C/fi not_active IP Right Cessation
- 1980-09-22 IL IL61106A patent/IL61106A/xx unknown
- 1980-09-22 DD DD80224047A patent/DD153050A5/de unknown
- 1980-09-22 GR GR62934A patent/GR70290B/el unknown
- 1980-09-22 NZ NZ195006A patent/NZ195006A/xx unknown
- 1980-09-23 ES ES495267A patent/ES8106710A1/es not_active Expired
- 1980-09-23 TR TR20766A patent/TR20766A/xx unknown
- 1980-09-23 ZA ZA00805889A patent/ZA805889B/xx unknown
- 1980-09-23 DK DK401180A patent/DK401180A/da not_active Application Discontinuation
- 1980-09-23 CA CA000360808A patent/CA1189516A/en not_active Expired
- 1980-09-23 PL PL1980226876A patent/PL124720B1/pl unknown
- 1980-09-23 EG EG583/80A patent/EG14311A/xx active
- 1980-09-23 AU AU62623/80A patent/AU537679B2/en not_active Ceased
- 1980-09-23 BR BR8006076A patent/BR8006076A/pt unknown
- 1980-09-24 HU HU802337A patent/HU186752B/hu unknown
- 1980-09-24 AR AR282632A patent/AR228744A1/es active
- 1980-09-24 JP JP13179580A patent/JPS5655379A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NZ195006A (en) | 1982-05-31 |
| DE3064292D1 (en) | 1983-08-25 |
| FI802985A7 (fi) | 1981-03-25 |
| DE2938534A1 (de) | 1981-04-23 |
| CA1189516A (en) | 1985-06-25 |
| PL226876A1 (ro) | 1981-10-02 |
| AR228744A1 (es) | 1983-04-15 |
| DK401180A (da) | 1981-03-25 |
| AU537679B2 (en) | 1984-07-05 |
| IL61106A (en) | 1984-09-30 |
| EG14311A (en) | 1983-09-30 |
| ATE4205T1 (de) | 1983-08-15 |
| FI66854B (fi) | 1984-08-31 |
| EP0025949B1 (de) | 1983-07-20 |
| PT71804B (en) | 1981-07-09 |
| EP0025949A1 (de) | 1981-04-01 |
| RO80677A (ro) | 1982-12-06 |
| US4359470A (en) | 1982-11-16 |
| DD153050A5 (de) | 1981-12-23 |
| FI66854C (fi) | 1984-12-10 |
| BR8006076A (pt) | 1981-04-07 |
| PT71804A (en) | 1980-10-01 |
| AU6262380A (en) | 1981-04-09 |
| IL61106A0 (en) | 1980-11-30 |
| PL124720B1 (en) | 1983-02-28 |
| ES495267A0 (es) | 1981-09-01 |
| NO802616L (no) | 1981-03-25 |
| HU186752B (en) | 1985-09-30 |
| JPS5655379A (en) | 1981-05-15 |
| GR70290B (ro) | 1982-09-03 |
| TR20766A (tr) | 1982-06-28 |
| ES8106710A1 (es) | 1981-09-01 |
| ZA805889B (en) | 1981-10-28 |
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