DD263219A5 - Herbizidzusammensetzung - Google Patents
Herbizidzusammensetzung Download PDFInfo
- Publication number
- DD263219A5 DD263219A5 DD87301766A DD30176687A DD263219A5 DD 263219 A5 DD263219 A5 DD 263219A5 DD 87301766 A DD87301766 A DD 87301766A DD 30176687 A DD30176687 A DD 30176687A DD 263219 A5 DD263219 A5 DD 263219A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- group
- formula
- radical
- compound
- methyl
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 43
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 17
- 239000004009 herbicide Substances 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 89
- 238000000034 method Methods 0.000 claims abstract description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 11
- 239000001301 oxygen Substances 0.000 claims abstract description 11
- 239000004094 surface-active agent Substances 0.000 claims abstract description 11
- 239000000460 chlorine Substances 0.000 claims abstract description 6
- 239000004480 active ingredient Substances 0.000 claims abstract description 5
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000011737 fluorine Substances 0.000 claims abstract description 4
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 4
- 230000008635 plant growth Effects 0.000 claims abstract description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 24
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 125000006413 ring segment Chemical group 0.000 claims description 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004849 alkoxymethyl group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- 125000003003 spiro group Chemical group 0.000 claims description 2
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- RGICCULPCWNRAB-UHFFFAOYSA-N 2-[2-(2-hexoxyethoxy)ethoxy]ethanol Chemical compound CCCCCCOCCOCCOCCO RGICCULPCWNRAB-UHFFFAOYSA-N 0.000 claims 1
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- -1 heterocyclic alcohols Chemical class 0.000 abstract description 36
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 3
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- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
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- 239000000047 product Substances 0.000 description 22
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- 239000002689 soil Substances 0.000 description 15
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- 239000002253 acid Substances 0.000 description 11
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- 238000005698 Diels-Alder reaction Methods 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
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- 238000006722 reduction reaction Methods 0.000 description 9
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- 239000002585 base Substances 0.000 description 6
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- 150000004795 grignard reagents Chemical class 0.000 description 6
- 239000012442 inert solvent Substances 0.000 description 6
- 239000000543 intermediate Substances 0.000 description 6
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- 238000002360 preparation method Methods 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 238000007363 ring formation reaction Methods 0.000 description 6
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- 239000002270 dispersing agent Substances 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- WRYLYDPHFGVWKC-JTQLQIEISA-N (R)-(-)-p-Menth-1-en-4-ol Natural products CC(C)[C@@]1(O)CCC(C)=CC1 WRYLYDPHFGVWKC-JTQLQIEISA-N 0.000 description 4
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- GSNUFIFRDBKVIE-UHFFFAOYSA-N 2,5-dimethylfuran Chemical compound CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 4
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- WRYLYDPHFGVWKC-UHFFFAOYSA-N 4-terpineol Chemical compound CC(C)C1(O)CCC(C)=CC1 WRYLYDPHFGVWKC-UHFFFAOYSA-N 0.000 description 4
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
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- 239000000376 reactant Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
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- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical class [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 125000005424 tosyloxy group Chemical group S(=O)(=O)(C1=CC=C(C)C=C1)O* 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 150000005199 trimethylbenzenes Chemical class 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
- C07D307/94—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom spiro-condensed with carbocyclic rings or ring systems, e.g. griseofulvins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85160986A | 1986-04-14 | 1986-04-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD263219A5 true DD263219A5 (de) | 1988-12-28 |
Family
ID=25311200
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD87301766A DD263219A5 (de) | 1986-04-14 | 1987-04-13 | Herbizidzusammensetzung |
Country Status (22)
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4782169A (en) * | 1986-10-06 | 1988-11-01 | E. I. Du Pont De Nemours And Company | 4,7-dioxatricyclo(3.2.1.03,6)octane ether |
| KR890701017A (ko) * | 1987-09-15 | 1989-12-19 | 제임스 제이.플린 | 선택적 옥사비사이클로알칸 |
| CN1031924A (zh) * | 1987-09-15 | 1989-03-29 | 纳幕尔杜邦公司 | 选择性氧杂二环烷 |
| US4828603A (en) * | 1988-03-21 | 1989-05-09 | E. I. Du Pont De Nemours And Company | Herbicidal oxatricyclo-nonane ethers |
| MY105897A (en) * | 1989-03-14 | 1994-11-30 | Du Pont | Selective oxabicycloalkanes. |
| AU637406B2 (en) * | 1989-09-11 | 1993-05-27 | E.I. Du Pont De Nemours And Company | Oxabicyclo ethers. |
| US5234900A (en) * | 1989-09-11 | 1993-08-10 | E. I. Du Pont De Nemours And Company | Herbicidal oxabicyclo ethers |
| WO1997016975A1 (en) * | 1994-05-11 | 1997-05-15 | John Selga | Herbicidal composition and method |
| AP2014007796A0 (en) | 2011-12-22 | 2014-07-31 | Alios Biopharma Inc | Substituted nucleosides, nucleotides and analogs thereof |
| USRE48171E1 (en) | 2012-03-21 | 2020-08-25 | Janssen Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
| US9441007B2 (en) | 2012-03-21 | 2016-09-13 | Alios Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
| CN105017275B (zh) * | 2015-07-16 | 2017-09-26 | 广西民族大学 | 以4‑萜品醇为原料合成2‑羟基‑1,4‑桉树脑的方法 |
| WO2024005209A1 (ja) * | 2022-06-30 | 2024-01-04 | 北興化学工業株式会社 | １，４－シネオール誘導体およびその中間体、上記誘導体を有効成分として含有する除草剤、除草剤の使用方法、ならびに農薬組成物を調製する方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4670041A (en) * | 1981-12-16 | 1987-06-02 | E. I. Du Pont De Nemours And Company | Oxabicycloalkane herbicides |
| US4410354A (en) * | 1982-02-01 | 1983-10-18 | Shell Oil Company | Spiro ether herbicides |
| US4525203A (en) * | 1984-06-15 | 1985-06-25 | Shell Oil Company | ((3,4,5,6-Tetrahydro-2H-pyran-2-yl)methoxy)oxabicycloalkane herbicides |
-
1987
- 1987-04-13 FR FR878705209A patent/FR2597101B1/fr not_active Expired - Fee Related
- 1987-04-13 HU HU871632A patent/HU201221B/hu not_active IP Right Cessation
- 1987-04-13 KR KR1019870003509A patent/KR950001023B1/ko not_active Expired - Lifetime
- 1987-04-13 GR GR870593A patent/GR870593B/el unknown
- 1987-04-13 ZA ZA872625A patent/ZA872625B/xx unknown
- 1987-04-13 ZW ZW68/87A patent/ZW6887A1/xx unknown
- 1987-04-13 JP JP62088996A patent/JPH0778051B2/ja not_active Expired - Lifetime
- 1987-04-13 IL IL82206A patent/IL82206A0/xx unknown
- 1987-04-13 AU AU71445/87A patent/AU596406B2/en not_active Expired - Fee Related
- 1987-04-13 ES ES8701073A patent/ES2005552A6/es not_active Expired
- 1987-04-13 GB GB8708790A patent/GB2188931B/en not_active Expired - Lifetime
- 1987-04-13 DK DK189587A patent/DK189587A/da not_active Application Discontinuation
- 1987-04-13 CH CH1451/87A patent/CH674364A5/fr not_active IP Right Cessation
- 1987-04-13 CN CN198787102716A patent/CN87102716A/zh active Pending
- 1987-04-13 PH PH35135A patent/PH23777A/en unknown
- 1987-04-13 BE BE8700385A patent/BE1002100A5/fr not_active IP Right Cessation
- 1987-04-13 DD DD87301766A patent/DD263219A5/de not_active IP Right Cessation
- 1987-04-13 PL PL1987265141A patent/PL265141A1/xx unknown
- 1987-04-13 BR BR8701754A patent/BR8701754A/pt unknown
- 1987-04-13 NL NL8700865A patent/NL8700865A/nl not_active Application Discontinuation
- 1987-04-13 IT IT8767301A patent/IT1207389B/it active
- 1987-04-13 DE DE19873712464 patent/DE3712464A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| CH674364A5 (enrdf_load_stackoverflow) | 1990-05-31 |
| HU201221B (en) | 1990-10-28 |
| KR950001023B1 (ko) | 1995-02-07 |
| ES2005552A6 (es) | 1989-03-16 |
| GB2188931A (en) | 1987-10-14 |
| DE3712464A1 (de) | 1987-10-15 |
| JPH0778051B2 (ja) | 1995-08-23 |
| KR880012607A (ko) | 1988-11-28 |
| PH23777A (en) | 1989-11-03 |
| IL82206A0 (en) | 1987-10-30 |
| AU7144587A (en) | 1987-10-15 |
| ZW6887A1 (en) | 1987-07-01 |
| GR870593B (en) | 1987-08-14 |
| DK189587A (da) | 1987-10-15 |
| IT1207389B (it) | 1989-05-17 |
| NL8700865A (nl) | 1987-11-02 |
| AU596406B2 (en) | 1990-05-03 |
| BR8701754A (pt) | 1988-01-12 |
| BE1002100A5 (fr) | 1990-07-03 |
| ZA872625B (en) | 1987-11-25 |
| GB2188931B (en) | 1990-10-10 |
| FR2597101B1 (fr) | 1993-08-27 |
| FR2597101A1 (fr) | 1987-10-16 |
| PL265141A1 (en) | 1989-03-06 |
| DK189587D0 (da) | 1987-04-13 |
| HUT45183A (en) | 1988-06-28 |
| GB8708790D0 (en) | 1987-05-20 |
| IT8767301A0 (it) | 1987-04-13 |
| CN87102716A (zh) | 1987-10-21 |
| JPS62249980A (ja) | 1987-10-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |