SU673136A3 - Гербицидное средство - Google Patents
Гербицидное средствоInfo
- Publication number
- SU673136A3 SU673136A3 SU772457129A SU2457129A SU673136A3 SU 673136 A3 SU673136 A3 SU 673136A3 SU 772457129 A SU772457129 A SU 772457129A SU 2457129 A SU2457129 A SU 2457129A SU 673136 A3 SU673136 A3 SU 673136A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- group
- alkoxy
- phenoxy
- active principle
- methyl
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims description 9
- 230000002363 herbicidal effect Effects 0.000 title claims 2
- 239000002253 acid Substances 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 9
- 230000035784 germination Effects 0.000 claims description 8
- 230000000694 effects Effects 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- -1 phenoxyphenoxy Chemical group 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 4
- 229910052801 chlorine Chemical group 0.000 claims description 4
- 239000000460 chlorine Chemical group 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 150000001767 cationic compounds Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 229910001411 inorganic cation Inorganic materials 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000004465 cycloalkenyloxy group Chemical group 0.000 claims 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 11
- 239000008187 granular material Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 241000287828 Gallus gallus Species 0.000 description 5
- 244000062793 Sorghum vulgare Species 0.000 description 5
- 235000019713 millet Nutrition 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- FZXRXKLUIMKDEL-UHFFFAOYSA-N 2-Methylpropyl propanoate Chemical compound CCC(=O)OCC(C)C FZXRXKLUIMKDEL-UHFFFAOYSA-N 0.000 description 3
- 244000291564 Allium cepa Species 0.000 description 3
- 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 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229940125898 compound 5 Drugs 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical class CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000008216 herbs Nutrition 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl group Polymers [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000010152 pollination Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
- C07C59/70—Ethers of hydroxy-acetic acid, e.g. substitutes on the ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/31—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
- C07C69/736—Ethers the hydroxy group of the ester being etherified with a hydroxy compound having the hydroxy group bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2609461A DE2609461C2 (de) | 1976-03-08 | 1976-03-08 | α-4-(Trifluormethylphenoxy)-phenoxy-propionsäuren und ihre Derivate, Verfahren zu ihrer Herstellung und sie enthaltende herbizide Mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU673136A3 true SU673136A3 (ru) | 1979-07-05 |
Family
ID=5971769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU772457129A SU673136A3 (ru) | 1976-03-08 | 1977-03-04 | Гербицидное средство |
Country Status (24)
| Country | Link |
|---|---|
| JP (1) | JPS52108939A (show.php) |
| AT (1) | AT350839B (show.php) |
| AU (1) | AU504699B2 (show.php) |
| BE (1) | BE852210A (show.php) |
| BR (1) | BR7701376A (show.php) |
| CA (1) | CA1110651A (show.php) |
| CH (1) | CH626227A5 (show.php) |
| DD (1) | DD128710A5 (show.php) |
| DE (1) | DE2609461C2 (show.php) |
| DK (1) | DK99077A (show.php) |
| ES (1) | ES456459A1 (show.php) |
| FR (1) | FR2343715A1 (show.php) |
| GB (1) | GB1563850A (show.php) |
| GR (1) | GR71188B (show.php) |
| HU (1) | HU179718B (show.php) |
| IE (1) | IE44423B1 (show.php) |
| IL (1) | IL51605A (show.php) |
| IT (1) | IT1078686B (show.php) |
| NL (1) | NL7702305A (show.php) |
| OA (1) | OA05588A (show.php) |
| PH (1) | PH12591A (show.php) |
| SU (1) | SU673136A3 (show.php) |
| TR (1) | TR19297A (show.php) |
| ZA (1) | ZA771297B (show.php) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0003114B1 (de) | 1978-01-18 | 1982-01-27 | Ciba-Geigy Ag | Herbizid wirksame ungesättigte Ester von 4-(3',5'-Dihalogenpyridyl -(2')-oxy)-alpha-phenoxypropionsäuren, Verfahren zu ihrer Herstellung sowie sie enthaltende herbizide Mittel und deren Verwendung |
| JPS6033389B2 (ja) * | 1979-02-22 | 1985-08-02 | 日産化学工業株式会社 | 複素環エ−テル系フェノシキ脂肪酸誘導体、その製造法および該誘導体を含有する除草剤 |
| US4391628A (en) * | 1981-02-16 | 1983-07-05 | Ciba-Geigy Corporation | 2-[4-(6-Haloquinoxalinyl-2-oxy)phenoxy]propionic acid esters |
| DE3219789A1 (de) * | 1982-05-26 | 1983-12-01 | Bayer Ag, 5090 Leverkusen | Phenoxypropionsaeure-derivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
| DE3318354A1 (de) * | 1983-05-20 | 1984-11-22 | Bayer Ag, 5090 Leverkusen | Optisch aktive propionsaeure-derivate |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2433067B2 (de) * | 1974-07-10 | 1977-11-24 | a- [4-(4" Trifluormethylphenoxy)-phenoxy] -propionsäuren und deren Derivate, Verfahren zu ihrer Herstellung und diese enthaltende herbizide Mittel Hoechst AG, 6000 Frankfurt | Alpha- eckige klammer auf 4-(4' trifluormethylphenoxy)-phenoxy eckige klammer zu -propionsaeuren und deren derivate, verfahren zu ihrer herstellung und diese enthaltende herbizide mittel |
| CS185694B2 (en) * | 1974-07-17 | 1978-10-31 | Ishihara Sangyo Kaisha | Herbicidal agent |
-
1976
- 1976-03-08 DE DE2609461A patent/DE2609461C2/de not_active Expired
-
1977
- 1977-03-02 ES ES456459A patent/ES456459A1/es not_active Expired
- 1977-03-03 NL NL7702305A patent/NL7702305A/xx not_active Application Discontinuation
- 1977-03-04 SU SU772457129A patent/SU673136A3/ru active
- 1977-03-04 ZA ZA00771297A patent/ZA771297B/xx unknown
- 1977-03-04 IT IT20955/77A patent/IT1078686B/it active
- 1977-03-04 DD DD7700197679A patent/DD128710A5/xx unknown
- 1977-03-05 GR GR52915A patent/GR71188B/el unknown
- 1977-03-07 OA OA56090A patent/OA05588A/xx unknown
- 1977-03-07 IE IE493/77A patent/IE44423B1/en unknown
- 1977-03-07 HU HU77HO1967A patent/HU179718B/hu unknown
- 1977-03-07 AT AT147477A patent/AT350839B/de not_active IP Right Cessation
- 1977-03-07 IL IL51605A patent/IL51605A/xx unknown
- 1977-03-07 CH CH281877A patent/CH626227A5/de not_active IP Right Cessation
- 1977-03-07 JP JP2399077A patent/JPS52108939A/ja active Pending
- 1977-03-07 CA CA273,307A patent/CA1110651A/en not_active Expired
- 1977-03-07 GB GB9460/77A patent/GB1563850A/en not_active Expired
- 1977-03-07 DK DK99077A patent/DK99077A/da not_active Application Discontinuation
- 1977-03-08 FR FR7706716A patent/FR2343715A1/fr active Granted
- 1977-03-08 BE BE175580A patent/BE852210A/xx not_active IP Right Cessation
- 1977-03-08 TR TR19297A patent/TR19297A/xx unknown
- 1977-03-08 PH PH19537A patent/PH12591A/en unknown
- 1977-03-08 BR BR7701376A patent/BR7701376A/pt unknown
- 1977-03-08 AU AU23016/77A patent/AU504699B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IL51605A0 (en) | 1977-05-31 |
| TR19297A (tr) | 1978-11-01 |
| PH12591A (en) | 1979-06-27 |
| DE2609461C2 (de) | 1984-11-22 |
| ATA147477A (de) | 1978-11-15 |
| BE852210A (fr) | 1977-09-08 |
| CH626227A5 (en) | 1981-11-13 |
| IE44423L (en) | 1977-09-08 |
| IT1078686B (it) | 1985-05-08 |
| DE2609461A1 (de) | 1977-09-22 |
| OA05588A (fr) | 1981-04-30 |
| FR2343715B1 (show.php) | 1981-12-11 |
| ES456459A1 (es) | 1978-02-16 |
| AT350839B (de) | 1979-06-25 |
| IL51605A (en) | 1980-10-26 |
| FR2343715A1 (fr) | 1977-10-07 |
| GB1563850A (en) | 1980-04-02 |
| IE44423B1 (en) | 1981-11-18 |
| JPS52108939A (en) | 1977-09-12 |
| AU2301677A (en) | 1978-09-14 |
| DK99077A (da) | 1977-09-09 |
| NL7702305A (nl) | 1977-09-12 |
| DD128710A5 (de) | 1977-12-07 |
| BR7701376A (pt) | 1978-05-02 |
| AU504699B2 (en) | 1979-10-25 |
| GR71188B (show.php) | 1983-04-11 |
| HU179718B (en) | 1982-11-29 |
| CA1110651A (en) | 1981-10-13 |
| ZA771297B (en) | 1978-01-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU1836012C (ru) | Способ защиты зерновых культур от фитотоксического действи феноксапропэтила | |
| JPS606603A (ja) | 栽培植物の保護の為のキノリン誘導体の使用方法 | |
| JP2606300B2 (ja) | 除草組成物 | |
| JPH0553762B2 (show.php) | ||
| US4334910A (en) | Plant-protective and pest-control agent | |
| SU673136A3 (ru) | Гербицидное средство | |
| IL43840A (en) | Derivatives of 2-substituted 1,3,4-oxadiazole-5-thiol and fungicidal compositions containing them | |
| US4531966A (en) | Herbicide compositions | |
| EP0064353B1 (en) | Use of 2,4-disubstituted-5-thiazolecarboxylic acids and derivatives for reducing injury to crop plants by acetamide herbicides | |
| JPS5841807A (ja) | 除草剤 | |
| JPS62148479A (ja) | 線虫および昆虫駆除用組成物 | |
| US4347366A (en) | 2-(Pyridylthio)pyridine-N-oxides | |
| US4391631A (en) | Herbicidal composition | |
| US4239527A (en) | 2-(Pyridylthio)pyridine-N-oxides | |
| US3998621A (en) | Triazine--antidote compositions and methods of use for cotton | |
| US4441914A (en) | Dichloroacetyl oxazolidine herbicide antidotes | |
| JPS5877802A (ja) | 除草剤 | |
| JPH0564921B2 (show.php) | ||
| JPH02262571A (ja) | ベンゾイソチアゾール、その製造方法およびこれを含有する有害生物駆除剤 | |
| JPS58188804A (ja) | 除草剤 | |
| JPH04198158A (ja) | ベンズアミド誘導体および除草剤 | |
| JPS60116661A (ja) | フエノキシアルカノイル誘導体、それらの製造方法および植物保護におけるそれらの用途 | |
| IL47617A (en) | Herbicidal compositions containing a n-(phenyl-carbamoyl)-4-methyl piperidine and a s-ethyl-n,n-dialkyl-thiocarbamate | |
| JPH01190673A (ja) | 置換テトラゾリノン化合物、その製造方法および除草剤組成物 | |
| JPS6033402B2 (ja) | 水田用除草組成物 |