FR2549831A1 - Nouveaux derives d'acides aryloxybenzoiques, et leur utilisation comme herbicides - Google Patents
Nouveaux derives d'acides aryloxybenzoiques, et leur utilisation comme herbicides Download PDFInfo
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- FR2549831A1 FR2549831A1 FR8312619A FR8312619A FR2549831A1 FR 2549831 A1 FR2549831 A1 FR 2549831A1 FR 8312619 A FR8312619 A FR 8312619A FR 8312619 A FR8312619 A FR 8312619A FR 2549831 A1 FR2549831 A1 FR 2549831A1
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- radical
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- halogen atom
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- 239000004009 herbicide Substances 0.000 title description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 83
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- 239000000203 mixture Substances 0.000 claims description 27
- 125000005843 halogen group Chemical group 0.000 claims description 24
- 239000004480 active ingredient Substances 0.000 claims description 23
- 230000002363 herbicidal effect Effects 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 19
- 238000002360 preparation method Methods 0.000 claims description 17
- 150000003254 radicals Chemical class 0.000 claims description 16
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- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000003880 polar aprotic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229940098458 powder spray Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- ARENMZZMCSLORU-UHFFFAOYSA-N propan-2-yl naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)OC(C)C)=CC=CC2=C1 ARENMZZMCSLORU-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003445 sucroses Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000004001 thioalkyl group Chemical group 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—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
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
Priority Applications (18)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8312619A FR2549831A1 (fr) | 1983-07-27 | 1983-07-27 | Nouveaux derives d'acides aryloxybenzoiques, et leur utilisation comme herbicides |
| IL72362A IL72362A0 (en) | 1983-07-27 | 1984-07-10 | Aryloxybenzoic acid derivatives,their preparation and their use as herbicides |
| NL8402312A NL8402312A (nl) | 1983-07-27 | 1984-07-20 | Aryloxybenzoezuur-derivaten en toepassing daarvan als herbiciden. |
| MA20408A MA20184A1 (fr) | 1983-07-27 | 1984-07-20 | Nouveaux derives d'acide aryloxybenzoiques et leur utilisation comme herbicides. |
| GR75409A GR82227B (enrdf_load_stackoverflow) | 1983-07-27 | 1984-07-24 | |
| ZA845763A ZA845763B (en) | 1983-07-27 | 1984-07-25 | New derivatives of aryloxybenzoic acids and their use as herbicides |
| GB08418958A GB2144125A (en) | 1983-07-27 | 1984-07-25 | Derivatives of aryloxybenzoic acids and their use as herbicides |
| DD84265641A DD218543A5 (de) | 1983-07-27 | 1984-07-25 | Herbizides mittel |
| IT22035/84A IT1178500B (it) | 1983-07-27 | 1984-07-25 | Derivati di acidi arilossibenzoici e loro impiego come erbicidi |
| AU31134/84A AU3113484A (en) | 1983-07-27 | 1984-07-25 | Tetrazole derivatives |
| LU85477A LU85477A1 (fr) | 1983-07-27 | 1984-07-25 | Nouveaux derives d'acides aryloxybenzoiques et leur utilisation comme herbicides |
| HU842878A HUT35252A (en) | 1983-07-27 | 1984-07-26 | Herbicides containing aryl-oxy-benzoic acid derivatives as active substances and process for preparing the active substances |
| DE19843427606 DE3427606A1 (de) | 1983-07-27 | 1984-07-26 | Aryloxybenzoesaeure-verbindungen |
| BR8403737A BR8403737A (pt) | 1983-07-27 | 1984-07-26 | Compostos,processos para preparacao de compostos,composicao herbicida e processo para a eliminacao seletiva das ervas daninhas das culturas |
| PT78983A PT78983B (fr) | 1983-07-27 | 1984-07-26 | Procede de preparation de nouveaux derives d'acides aryloxybenzoiques et de compositions herbicides les contenant |
| BE0/213394A BE900237A (fr) | 1983-07-27 | 1984-07-26 | Nouveaux derives d'acides aryloxybenzoiques et leur utilisation comme herbicides. |
| OA58350A OA07756A (fr) | 1983-07-27 | 1984-07-27 | Nouveaux dérivés d'acides aryloxybenzoïques et leur utilisation comme herbicides. |
| KR1019840004486A KR850001180A (ko) | 1983-07-27 | 1984-07-27 | 아릴옥시벤조산 유도체의 제조방법 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8312619A FR2549831A1 (fr) | 1983-07-27 | 1983-07-27 | Nouveaux derives d'acides aryloxybenzoiques, et leur utilisation comme herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FR2549831A1 true FR2549831A1 (fr) | 1985-02-01 |
Family
ID=9291276
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR8312619A Pending FR2549831A1 (fr) | 1983-07-27 | 1983-07-27 | Nouveaux derives d'acides aryloxybenzoiques, et leur utilisation comme herbicides |
Country Status (18)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU209793B (en) * | 1990-09-25 | 1994-11-28 | Chinoin Gyogyszer Es Vegyeszet | Process for the production of pyrido[1,2-a]pyrimidine-derivatives and pharmaceutical compositions containing the same |
| CN105829286B (zh) | 2013-12-20 | 2019-05-31 | 诺华股份有限公司 | 作为lta4h抑制剂的杂芳基丁酸衍生物 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2521980A1 (de) * | 1974-05-28 | 1975-12-18 | Yoshitomi Pharmaceutical | 1h-tetrazol-derivate |
| FR2346329A1 (fr) * | 1976-03-31 | 1977-10-28 | Hoechst Ag | Derives d'acides phenoxy-phenoxy-alcanoiques et composes apparentes, utilisables dans des produits herbicides |
| EP0020052A1 (en) * | 1979-05-16 | 1980-12-10 | Rohm And Haas Company | Novel substituted nitrodiphenyl ethers, herbicidal compositions containing them, processes for the preparation thereof and the use thereof for combating weeds |
| DE2933962A1 (de) * | 1979-08-22 | 1981-03-26 | Hoechst Ag, 65929 Frankfurt | Verfahren zur herstellung von 4,5-dichlor-imidazolen. |
-
1983
- 1983-07-27 FR FR8312619A patent/FR2549831A1/fr active Pending
-
1984
- 1984-07-10 IL IL72362A patent/IL72362A0/xx unknown
- 1984-07-20 NL NL8402312A patent/NL8402312A/nl not_active Application Discontinuation
- 1984-07-20 MA MA20408A patent/MA20184A1/fr unknown
- 1984-07-24 GR GR75409A patent/GR82227B/el unknown
- 1984-07-25 DD DD84265641A patent/DD218543A5/de unknown
- 1984-07-25 GB GB08418958A patent/GB2144125A/en not_active Withdrawn
- 1984-07-25 AU AU31134/84A patent/AU3113484A/en not_active Abandoned
- 1984-07-25 LU LU85477A patent/LU85477A1/fr unknown
- 1984-07-25 IT IT22035/84A patent/IT1178500B/it active
- 1984-07-25 ZA ZA845763A patent/ZA845763B/xx unknown
- 1984-07-26 DE DE19843427606 patent/DE3427606A1/de not_active Withdrawn
- 1984-07-26 PT PT78983A patent/PT78983B/pt unknown
- 1984-07-26 BE BE0/213394A patent/BE900237A/fr not_active IP Right Cessation
- 1984-07-26 BR BR8403737A patent/BR8403737A/pt unknown
- 1984-07-26 HU HU842878A patent/HUT35252A/hu unknown
- 1984-07-27 OA OA58350A patent/OA07756A/xx unknown
- 1984-07-27 KR KR1019840004486A patent/KR850001180A/ko not_active Abandoned
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2521980A1 (de) * | 1974-05-28 | 1975-12-18 | Yoshitomi Pharmaceutical | 1h-tetrazol-derivate |
| FR2346329A1 (fr) * | 1976-03-31 | 1977-10-28 | Hoechst Ag | Derives d'acides phenoxy-phenoxy-alcanoiques et composes apparentes, utilisables dans des produits herbicides |
| EP0020052A1 (en) * | 1979-05-16 | 1980-12-10 | Rohm And Haas Company | Novel substituted nitrodiphenyl ethers, herbicidal compositions containing them, processes for the preparation thereof and the use thereof for combating weeds |
| DE2933962A1 (de) * | 1979-08-22 | 1981-03-26 | Hoechst Ag, 65929 Frankfurt | Verfahren zur herstellung von 4,5-dichlor-imidazolen. |
Also Published As
| Publication number | Publication date |
|---|---|
| KR850001180A (ko) | 1985-03-16 |
| PT78983B (fr) | 1986-10-23 |
| IL72362A0 (en) | 1984-11-30 |
| OA07756A (fr) | 1985-08-30 |
| GB8418958D0 (en) | 1984-08-30 |
| HUT35252A (en) | 1985-06-28 |
| ZA845763B (en) | 1985-03-27 |
| BR8403737A (pt) | 1985-07-02 |
| DE3427606A1 (de) | 1985-02-07 |
| GB2144125A (en) | 1985-02-27 |
| LU85477A1 (fr) | 1986-02-12 |
| BE900237A (fr) | 1985-01-28 |
| AU3113484A (en) | 1985-01-31 |
| PT78983A (fr) | 1984-08-01 |
| IT8422035A0 (it) | 1984-07-25 |
| GR82227B (enrdf_load_stackoverflow) | 1984-12-13 |
| NL8402312A (nl) | 1985-02-18 |
| IT1178500B (it) | 1987-09-09 |
| MA20184A1 (fr) | 1985-04-01 |
| DD218543A5 (de) | 1985-02-13 |
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