SU1676435A3 - Способ борьбы с сорн ками - Google Patents
Способ борьбы с сорн ками Download PDFInfo
- Publication number
- SU1676435A3 SU1676435A3 SU864028283A SU4028283A SU1676435A3 SU 1676435 A3 SU1676435 A3 SU 1676435A3 SU 864028283 A SU864028283 A SU 864028283A SU 4028283 A SU4028283 A SU 4028283A SU 1676435 A3 SU1676435 A3 SU 1676435A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- benzene
- chlorine
- struggle against
- against weeds
- methyl
- Prior art date
Links
- 241000196324 Embryophyta Species 0.000 title claims description 8
- 238000000034 method Methods 0.000 title claims description 4
- 239000002689 soil Substances 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Chemical group 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000013256 coordination polymer Substances 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 27
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- YNWKEXMSQQUMEL-UHFFFAOYSA-N 2-chloro-4-(trifluoromethyl)phenol Chemical compound OC1=CC=C(C(F)(F)F)C=C1Cl YNWKEXMSQQUMEL-UHFFFAOYSA-N 0.000 description 1
- VGUWZCUCNQXGBU-UHFFFAOYSA-N 3-[(4-methylpiperazin-1-yl)methyl]-5-nitro-1h-indole Chemical compound C1CN(C)CCN1CC1=CNC2=CC=C([N+]([O-])=O)C=C12 VGUWZCUCNQXGBU-UHFFFAOYSA-N 0.000 description 1
- KGPHNHSAYAXSOW-UHFFFAOYSA-N 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl chloride Chemical compound C1=C(C(Cl)=O)C([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1Cl KGPHNHSAYAXSOW-UHFFFAOYSA-N 0.000 description 1
- CJBJFLYZIVJXTF-UHFFFAOYSA-N C1=CC(=C(C=C1F)[N+](=O)[O-])C(=O)C(C(=O)O)C(=O)O Chemical compound C1=CC(=C(C=C1F)[N+](=O)[O-])C(=O)C(C(=O)O)C(=O)O CJBJFLYZIVJXTF-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- SLUNEGLMXGHOLY-UHFFFAOYSA-N benzene;hexane Chemical compound CCCCCC.C1=CC=CC=C1 SLUNEGLMXGHOLY-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- KDIFRLZXBPGPJS-UHFFFAOYSA-N diethyl 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl]propanedioate Chemical compound C(C)OC(C(C(=O)OCC)C(C1=C(C=CC(=C1)OC1=C(C=C(C=C1)C(F)(F)F)Cl)[N+](=O)[O-])=O)=O KDIFRLZXBPGPJS-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 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
- A01N37/42—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 within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
-
- 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
- A01N37/48—Nitro-carboxylic acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/56—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (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 |
|---|---|---|---|
| HU853797A HU196884B (en) | 1985-10-01 | 1985-10-01 | Herbicides comprising phenoxy-benzoyl-malon ester derivatives as active ingredient and process for producing the active ingredients |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1676435A3 true SU1676435A3 (ru) | 1991-09-07 |
Family
ID=10965547
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU864028283A SU1676435A3 (ru) | 1985-10-01 | 1986-09-30 | Способ борьбы с сорн ками |
Country Status (14)
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5925795A (en) * | 1996-09-16 | 1999-07-20 | Zeneca Limited | Processes for the preparation of aryl-β-diketones, arylpyrimidine ketones and crop protection intermediates |
-
1985
- 1985-10-01 HU HU853797A patent/HU196884B/hu not_active IP Right Cessation
-
1986
- 1986-09-08 IL IL79974A patent/IL79974A/xx unknown
- 1986-09-18 CH CH3682/86A patent/CH676595A5/de not_active IP Right Cessation
- 1986-09-24 DE DE19863632492 patent/DE3632492A1/de not_active Withdrawn
- 1986-09-25 DD DD86294689A patent/DD249840A5/de not_active IP Right Cessation
- 1986-09-25 DD DD86301113A patent/DD255729A5/de not_active IP Right Cessation
- 1986-09-30 AU AU63266/86A patent/AU595834B2/en not_active Ceased
- 1986-09-30 FR FR8613597A patent/FR2587998B1/fr not_active Expired
- 1986-09-30 SU SU864028283A patent/SU1676435A3/ru active
- 1986-09-30 JP JP61230188A patent/JPS6281353A/ja active Pending
- 1986-09-30 GB GB8623486A patent/GB2181133B/en not_active Expired
- 1986-09-30 SE SE8604148A patent/SE8604148L/ not_active Application Discontinuation
- 1986-10-01 CS CS705886A patent/CS273620B2/cs unknown
- 1986-10-01 BE BE0/217241A patent/BE905534A/fr not_active IP Right Cessation
- 1986-10-01 NL NL8602481A patent/NL8602481A/nl not_active Application Discontinuation
Non-Patent Citations (1)
| Title |
|---|
| Патент СССР № 1152506, кл. А 01 N 37/40, С 07 С 69/76, 1981. * |
Also Published As
| Publication number | Publication date |
|---|---|
| DD249840A5 (de) | 1987-09-23 |
| HUT41590A (en) | 1987-05-28 |
| CS705886A2 (en) | 1990-08-14 |
| HU196884B (en) | 1989-02-28 |
| BE905534A (fr) | 1987-02-02 |
| NL8602481A (nl) | 1987-05-04 |
| GB2181133A (en) | 1987-04-15 |
| AU6326686A (en) | 1987-04-09 |
| FR2587998B1 (fr) | 1988-08-05 |
| SE8604148L (sv) | 1987-04-02 |
| GB2181133B (en) | 1989-03-22 |
| IL79974A0 (en) | 1986-12-31 |
| SE8604148D0 (sv) | 1986-09-30 |
| CS273620B2 (en) | 1991-03-12 |
| DE3632492A1 (de) | 1987-04-16 |
| IL79974A (en) | 1990-09-17 |
| DD255729A5 (de) | 1988-04-13 |
| FR2587998A1 (fr) | 1987-04-03 |
| CH676595A5 (enrdf_load_stackoverflow) | 1991-02-15 |
| JPS6281353A (ja) | 1987-04-14 |
| AU595834B2 (en) | 1990-04-12 |
| GB8623486D0 (en) | 1986-11-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU1715190A3 (ru) | Способ борьбы с нежелательными растени ми | |
| SU1356950A3 (ru) | Способ борьбы с нежелательной растительностью | |
| RU2055836C1 (ru) | Производные пиразола или их соли с основаниями | |
| CA1311240C (en) | Arylcarboxylic acid derivatives, the preparation and use thereof | |
| DK154074B (da) | Alfa-(4-(5 eller 3,5 substitueret pyridyl-2-oxy)-phenoxy)-alkan-carboxylsyrer eller derivater deraf til anvendelse som herbicider, herbicidt middel samt fremgangsmaader til bekaempelse af ukrudt | |
| JPS6344747B2 (enrdf_load_stackoverflow) | ||
| CH650496A5 (de) | N-substituierte tetrahydrophthalimidderivate. | |
| DK155935B (da) | Substituerede diphenylethere, herbicide praeparater indeholdende disse forbindelser samt fremgangsmaade til bekaempelse af ukrudt | |
| DE2649706A1 (de) | Phenoxypropan-verbindungen, deren verwendung als herbicide und diese verbindung enthaltende mittel | |
| IL44187A (en) | 5-acetamido-2,4 dimethyltrifluoromethanesulfonanilide and its preparation | |
| DE2118190C2 (de) | Perfluoralkylsulfonanilide und diese Verbindungen enthaltende herbizide Mittel | |
| JP2714479B2 (ja) | ２―（２’，３’，４’―三置換ベンゾイル）―１，３―シクロヘキサンジオン | |
| JPH0339482B2 (enrdf_load_stackoverflow) | ||
| US4235621A (en) | 2-Substituted phenoxy-3-chloro-5-trifluoromethyl pyridine useful as a herbicide | |
| BG62310B2 (bg) | Хетероциклични диони като пестициди и растежни регулатори | |
| FR2597866A1 (fr) | Derives du pyrazole, procede de preparation de ceux-ci et fongicide les contenant. | |
| US4013444A (en) | Inhibiting grass growth with 5-acetamido-2,4-dimethyltrifluoromethanesulfonanilide | |
| SU1676435A3 (ru) | Способ борьбы с сорн ками | |
| EP0119892B1 (fr) | Nouveau dérivés de l'hydroxylamine, leur procédé de préparation, leur application comme facteur de croissance des végétaux et les compositions les renfermant | |
| US4164412A (en) | Perfluoroalkylsulfonamidoaryl compounds | |
| SU1584737A3 (ru) | Способ борьбы с сорн ками | |
| SU1616516A3 (ru) | Способ получени производных 2-нитро-5-(пиридилокси)бензогидроксамовой кислоты | |
| US4039635A (en) | Soil fungicidal phosphorothioate | |
| BE865114A (fr) | Esters et thiolesters d'acides amines, procede d'obtention et application a titre pesticides. | |
| SU1440324A3 (ru) | Гербицидна композици |