SU1356958A3 - Способ получени оксимов - Google Patents
Способ получени оксимов Download PDFInfo
- Publication number
- SU1356958A3 SU1356958A3 SU833564200A SU3564200A SU1356958A3 SU 1356958 A3 SU1356958 A3 SU 1356958A3 SU 833564200 A SU833564200 A SU 833564200A SU 3564200 A SU3564200 A SU 3564200A SU 1356958 A3 SU1356958 A3 SU 1356958A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- herbicide
- antidote
- general formula
- seeds
- compounds
- Prior art date
Links
- 150000002923 oximes Chemical class 0.000 title claims abstract 7
- 238000000034 method Methods 0.000 title description 8
- -1 alkali metal cation Chemical class 0.000 claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 claims abstract description 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract 4
- 150000002367 halogens Chemical class 0.000 claims abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract 2
- 125000002947 alkylene group Chemical group 0.000 claims abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 2
- 239000001257 hydrogen Substances 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000003701 inert diluent Substances 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
- 239000004009 herbicide Substances 0.000 abstract description 45
- 239000000729 antidote Substances 0.000 abstract description 37
- 150000001875 compounds Chemical class 0.000 abstract description 21
- 230000035784 germination Effects 0.000 abstract description 11
- 230000000694 effects Effects 0.000 abstract description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract description 6
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 abstract description 4
- 230000000885 phytotoxic effect Effects 0.000 abstract description 4
- 229960001413 acetanilide Drugs 0.000 abstract description 3
- 229940075522 antidotes Drugs 0.000 abstract description 3
- 230000006378 damage Effects 0.000 abstract description 3
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 230000002538 fungal effect Effects 0.000 abstract description 2
- 238000003786 synthesis reaction Methods 0.000 abstract description 2
- 150000002170 ethers Chemical class 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 description 39
- 241000196324 Embryophyta Species 0.000 description 20
- 239000000203 mixture Substances 0.000 description 15
- 239000002689 soil Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 10
- 244000062793 Sorghum vulgare Species 0.000 description 9
- 235000019713 millet Nutrition 0.000 description 9
- 230000001681 protective effect Effects 0.000 description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 241000209094 Oryza Species 0.000 description 6
- 235000007164 Oryza sativa Nutrition 0.000 description 5
- 235000009566 rice Nutrition 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 238000009331 sowing Methods 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 240000006394 Sorghum bicolor Species 0.000 description 3
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 description 2
- 206010017533 Fungal infection Diseases 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 208000031888 Mycoses Diseases 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- LTAXKDMBDOACER-UHFFFAOYSA-N n-(1,3-dioxolan-2-ylmethoxy)-2,2,2-trifluoro-1-phenylethanimine Chemical compound C=1C=CC=CC=1C(C(F)(F)F)=NOCC1OCCO1 LTAXKDMBDOACER-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 1
- WZZBNLYBHUDSHF-DHLKQENFSA-N 1-[(3s,4s)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone Chemical compound CC1=NC2=CN=C3C=C(F)C(C=4C(=CC(OC=5N=CC=CN=5)=CC=4)Cl)=CC3=C2N1[C@H]1CCN(C(=O)CO)C[C@@H]1F WZZBNLYBHUDSHF-DHLKQENFSA-N 0.000 description 1
- YQYRYHNCVCFNHU-UHFFFAOYSA-N 1-ethyl-4-phenyl-3,6-dihydro-2h-pyridine Chemical compound C1N(CC)CCC(C=2C=CC=CC=2)=C1 YQYRYHNCVCFNHU-UHFFFAOYSA-N 0.000 description 1
- CKIIJIDEWWXQEA-UHFFFAOYSA-N 2-(bromomethyl)-1,3-dioxolane Chemical compound BrCC1OCCO1 CKIIJIDEWWXQEA-UHFFFAOYSA-N 0.000 description 1
- UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 description 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 1
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 1
- XKTYXVDYIKIYJP-UHFFFAOYSA-N 3h-dioxole Chemical compound C1OOC=C1 XKTYXVDYIKIYJP-UHFFFAOYSA-N 0.000 description 1
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 239000005583 Metribuzin Substances 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 230000009526 moderate injury Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/04—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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
- C07D309/06—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/18—Radicals substituted by singly bound oxygen or sulfur atoms
- C07D317/22—Radicals substituted by singly bound oxygen or sulfur atoms etherified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D321/00—Heterocyclic compounds containing rings having two oxygen atoms as the only ring hetero atoms, not provided for by groups C07D317/00 - C07D319/00
- C07D321/02—Seven-membered rings
- C07D321/04—Seven-membered rings not condensed with other rings
- C07D321/06—1,3-Dioxepines; Hydrogenated 1,3-dioxepines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/02—Five-membered rings
- C07D339/06—Five-membered rings having the hetero atoms in positions 1 and 3, e.g. cyclic dithiocarbonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/08—Six-membered rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Furan Compounds (AREA)
- Pyrane Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Indole Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LTRP1277A LT2606B (lt) | 1982-03-15 | 1993-09-29 | Oksimu gavimo budas |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH160982 | 1982-03-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1356958A3 true SU1356958A3 (ru) | 1987-11-30 |
Family
ID=4214431
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU833564200A SU1356958A3 (ru) | 1982-03-15 | 1983-03-14 | Способ получени оксимов |
Country Status (21)
| Country | Link |
|---|---|
| US (3) | US4530716A (enExample) |
| EP (1) | EP0089313B1 (enExample) |
| JP (1) | JPS58170745A (enExample) |
| AR (1) | AR241243A1 (enExample) |
| AT (1) | ATE13053T1 (enExample) |
| BR (1) | BR8301263A (enExample) |
| CA (1) | CA1205477A (enExample) |
| CS (1) | CS235315B2 (enExample) |
| DE (1) | DE3360154D1 (enExample) |
| ES (1) | ES520579A0 (enExample) |
| GR (1) | GR77161B (enExample) |
| HU (1) | HU191606B (enExample) |
| IL (1) | IL68121A (enExample) |
| LV (1) | LV10149A (enExample) |
| MX (1) | MX157788A (enExample) |
| MY (1) | MY8700807A (enExample) |
| OA (1) | OA07341A (enExample) |
| PT (1) | PT76384B (enExample) |
| RO (1) | RO86646B (enExample) |
| SU (1) | SU1356958A3 (enExample) |
| ZA (1) | ZA831735B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2126790C1 (ru) * | 1990-05-09 | 1999-02-27 | Басф Аг | Циклогексеноноксимовый эфир и его сельскохозяйственно пригодные соли |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE13053T1 (de) * | 1982-03-15 | 1985-05-15 | Ciba Geigy Ag | Neue oximaether, verfahren zu ihrer herstellung, mittel die die neuen oximaether enthalten und ihre verwendung. |
| EP0092517B1 (de) * | 1982-04-16 | 1986-03-12 | Ciba-Geigy Ag | Neue Oximäther, Verfahren zu ihrer Herstellung, Mittel die die neuen Oximäther enthalten und ihre Verwendung |
| DE3481031D1 (de) * | 1983-04-12 | 1990-02-22 | Ciba Geigy Ag | Herbizides mittel. |
| IL75858A (en) * | 1984-07-31 | 1989-02-28 | Commw Scient Ind Res Org | Substituted benzyl ethers of oximes,their production and their use as arthropodicides |
| US5201933A (en) * | 1988-08-01 | 1993-04-13 | Monsanto Company | Safening herbicidal benzoic acid derivatives |
| DE4014171A1 (de) * | 1990-05-03 | 1991-11-07 | Basf Ag | Cyanochinolinverbindungen |
| US5266726A (en) * | 1990-10-22 | 1993-11-30 | Ciba-Geigy Corporation | Sterically hindered oxime color improvers for polyolefin processing |
| US5134183A (en) * | 1990-10-22 | 1992-07-28 | Ciba-Geigy Corporation | Sterically hindered oxime color improvers for polyolefin processing |
| US5541148A (en) * | 1992-07-08 | 1996-07-30 | Ciba-Geigy Corporation | Selective safened herbicidal composition comprising 2-ethoxycarbonyl-3-(4,6-dimethoxypyrimidine-2-yl) oxy-pyridine and an acylsulfamoylphenyl-urea safener |
| US6342466B1 (en) * | 1999-09-02 | 2002-01-29 | Clariant Finance (Bvi) Limited | Biodegradable solutions of biologically active compounds |
| CN109938042B (zh) * | 2019-04-25 | 2021-04-27 | 河北省农林科学院谷子研究所 | 一种高粱田化学除草用种衣剂及除草方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH632130A5 (en) * | 1977-03-02 | 1982-09-30 | Ciba Geigy Ag | Compositions on the basis of oxime ethers, oxime esters or oxime carbamates which are suitable in agriculture for crop protection |
| IT1110460B (it) * | 1977-03-02 | 1985-12-23 | Ciba Geigy Ag | Prodotti che favoriscono la crescita delle piante e prodotti che proteggono le piante a base di eteri di ossime e di esteri di ossime loro preparazione e loro impiego |
| US4347372A (en) * | 1978-09-01 | 1982-08-31 | Ciba-Geigy Corporation | Benzoxazolyl-glyoxylonitrile-2-oxime ether derivatives |
| US4269775A (en) * | 1978-09-01 | 1981-05-26 | Ciba-Geigy Corporation | Oxime derivatives for protecting plant crops |
| ATE13053T1 (de) * | 1982-03-15 | 1985-05-15 | Ciba Geigy Ag | Neue oximaether, verfahren zu ihrer herstellung, mittel die die neuen oximaether enthalten und ihre verwendung. |
| EP0092517B1 (de) * | 1982-04-16 | 1986-03-12 | Ciba-Geigy Ag | Neue Oximäther, Verfahren zu ihrer Herstellung, Mittel die die neuen Oximäther enthalten und ihre Verwendung |
-
1983
- 1983-03-09 AT AT83810097T patent/ATE13053T1/de not_active IP Right Cessation
- 1983-03-09 DE DE8383810097T patent/DE3360154D1/de not_active Expired
- 1983-03-09 EP EP83810097A patent/EP0089313B1/de not_active Expired
- 1983-03-10 US US06/473,905 patent/US4530716A/en not_active Expired - Lifetime
- 1983-03-11 CA CA000423453A patent/CA1205477A/en not_active Expired
- 1983-03-14 RO RO110314A patent/RO86646B/ro unknown
- 1983-03-14 SU SU833564200A patent/SU1356958A3/ru active
- 1983-03-14 IL IL68121A patent/IL68121A/xx not_active IP Right Cessation
- 1983-03-14 ES ES520579A patent/ES520579A0/es active Granted
- 1983-03-14 ZA ZA831735A patent/ZA831735B/xx unknown
- 1983-03-14 CS CS831734A patent/CS235315B2/cs unknown
- 1983-03-14 MX MX6672A patent/MX157788A/es unknown
- 1983-03-14 GR GR70784A patent/GR77161B/el unknown
- 1983-03-14 AR AR83292374A patent/AR241243A1/es active
- 1983-03-14 PT PT76384A patent/PT76384B/pt not_active IP Right Cessation
- 1983-03-14 HU HU83859A patent/HU191606B/hu not_active IP Right Cessation
- 1983-03-14 BR BR8301263A patent/BR8301263A/pt not_active IP Right Cessation
- 1983-03-15 JP JP58043017A patent/JPS58170745A/ja active Granted
- 1983-03-15 OA OA57935A patent/OA07341A/xx unknown
-
1985
- 1985-05-13 US US06/733,352 patent/US4576628A/en not_active Expired - Lifetime
- 1985-05-13 US US06/733,353 patent/US4707182A/en not_active Expired - Lifetime
-
1987
- 1987-12-30 MY MY807/87A patent/MY8700807A/xx unknown
-
1993
- 1993-06-30 LV LV930874A patent/LV10149A/xx unknown
Non-Patent Citations (1)
| Title |
|---|
| Вейганд-Хильгетаг.Методы эксперимента в органической химии. МоГ Хими 1968, Со 395о * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2126790C1 (ru) * | 1990-05-09 | 1999-02-27 | Басф Аг | Циклогексеноноксимовый эфир и его сельскохозяйственно пригодные соли |
Also Published As
| Publication number | Publication date |
|---|---|
| US4530716A (en) | 1985-07-23 |
| EP0089313A1 (de) | 1983-09-21 |
| CA1205477A (en) | 1986-06-03 |
| IL68121A (en) | 1986-11-30 |
| JPS58170745A (ja) | 1983-10-07 |
| CS235315B2 (en) | 1985-05-15 |
| MX157788A (es) | 1988-12-15 |
| JPH0124140B2 (enExample) | 1989-05-10 |
| AR241243A1 (es) | 1992-03-31 |
| RO86646A (ro) | 1985-04-17 |
| OA07341A (fr) | 1984-08-31 |
| US4576628A (en) | 1986-03-18 |
| HU191606B (en) | 1987-03-30 |
| BR8301263A (pt) | 1983-11-22 |
| RO86646B (ro) | 1985-05-03 |
| ES8500222A1 (es) | 1984-11-01 |
| ES520579A0 (es) | 1984-11-01 |
| IL68121A0 (en) | 1983-06-15 |
| MY8700807A (en) | 1987-12-31 |
| US4707182A (en) | 1987-11-17 |
| DE3360154D1 (en) | 1985-06-05 |
| EP0089313B1 (de) | 1985-05-02 |
| GR77161B (enExample) | 1984-09-10 |
| ATE13053T1 (de) | 1985-05-15 |
| PT76384A (en) | 1983-04-01 |
| ZA831735B (en) | 1983-12-28 |
| LV10149A (lv) | 1994-10-20 |
| PT76384B (en) | 1986-02-03 |
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