DE2416139A1 - Herbicide - Google Patents
HerbicideInfo
- Publication number
- DE2416139A1 DE2416139A1 DE2416139A DE2416139A DE2416139A1 DE 2416139 A1 DE2416139 A1 DE 2416139A1 DE 2416139 A DE2416139 A DE 2416139A DE 2416139 A DE2416139 A DE 2416139A DE 2416139 A1 DE2416139 A1 DE 2416139A1
- Authority
- DE
- Germany
- Prior art keywords
- herbicides
- herbicide
- active ingredient
- millet
- active
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000004009 herbicide Substances 0.000 title claims description 24
- 230000002363 herbicidal effect Effects 0.000 title description 5
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 240000008042 Zea mays Species 0.000 description 5
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 5
- 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 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 235000009973 maize Nutrition 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000002688 persistence Effects 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 240000005528 Arctium lappa Species 0.000 description 2
- 235000003130 Arctium lappa Nutrition 0.000 description 2
- 235000008078 Arctium minus Nutrition 0.000 description 2
- 235000007320 Avena fatua Nutrition 0.000 description 2
- 244000075850 Avena orientalis Species 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- 244000056139 Brassica cretica Species 0.000 description 2
- 235000003351 Brassica cretica Nutrition 0.000 description 2
- 235000003343 Brassica rupestris Nutrition 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 240000004385 Centaurea cyanus Species 0.000 description 2
- 235000005940 Centaurea cyanus Nutrition 0.000 description 2
- 241000251730 Chondrichthyes Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 235000021536 Sugar beet Nutrition 0.000 description 2
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- -1 alkylene radicals Chemical class 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 2
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 229940060367 inert ingredients Drugs 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 235000019713 millet Nutrition 0.000 description 2
- 235000010460 mustard Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical class NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 description 1
- 240000002245 Acer pensylvanicum Species 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- 235000005474 African couch grass Nutrition 0.000 description 1
- 241000219479 Aizoaceae Species 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 240000003173 Drymaria cordata Species 0.000 description 1
- 244000078127 Eleusine coracana Species 0.000 description 1
- 235000013499 Eleusine coracana subsp coracana Nutrition 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241001520106 Eustachys Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241000721701 Lynx Species 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- 235000009071 Mesembryanthemum crystallinum Nutrition 0.000 description 1
- 244000070788 Milium effusum Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 240000005498 Setaria italica Species 0.000 description 1
- 235000001155 Setaria leucopila Nutrition 0.000 description 1
- 241000820163 Setaria leucopila Species 0.000 description 1
- 241000272534 Struthio camelus Species 0.000 description 1
- 244000204900 Talipariti tiliaceum Species 0.000 description 1
- 244000274883 Urtica dioica Species 0.000 description 1
- 235000009108 Urtica dioica Nutrition 0.000 description 1
- 235000005545 Veronica americana Nutrition 0.000 description 1
- 240000005592 Veronica officinalis Species 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 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
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02J—CIRCUIT ARRANGEMENTS OR SYSTEMS FOR SUPPLYING OR DISTRIBUTING ELECTRIC POWER; SYSTEMS FOR STORING ELECTRIC ENERGY
- H02J7/00—Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries
- H02J7/0013—Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries acting upon several batteries simultaneously or sequentially
- H02J7/0025—Sequential battery discharge in systems with a plurality of batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2416139A DE2416139A1 (de) | 1974-04-03 | 1974-04-03 | Herbicide |
| NL7503091A NL7503091A (nl) | 1974-04-03 | 1975-03-14 | Werkwijze voor het bereiden van herbiciden. |
| GB1168775A GB1478227A (en) | 1974-04-03 | 1975-03-20 | Piperidino carboxanilides and their use as herbicides |
| AU79335/75A AU483571B2 (en) | 1974-04-03 | 1975-03-20 | Herbicides |
| US05/562,476 US3972707A (en) | 1974-04-03 | 1975-03-27 | N-(phenylcarbamoyl)-4-methylpiperidine herbicides compositions and herbicidal method |
| JP50039009A JPS5243887B2 (enExample) | 1974-04-03 | 1975-03-31 | |
| IL46984A IL46984A (en) | 1974-04-03 | 1975-04-01 | N-(phenyl(or 4'-fluorophenyl)-carbamoyl)-4-methylpiperidine derivatives and herbicidal compositions containing them |
| CA223,437A CA1041099A (en) | 1974-04-03 | 1975-04-01 | N-(phenylcarbamoyl)-4-methylpiperidine herbicides compositions and herbicidal method |
| FR7510236A FR2266459A1 (enExample) | 1974-04-03 | 1975-04-02 | |
| AT249275A AT340717B (de) | 1974-04-03 | 1975-04-02 | Herbizide |
| ES436229A ES436229A1 (es) | 1974-04-03 | 1975-04-02 | Procedimiento para la preparacion de carboxanilido-4-metil- piperidinas. |
| CH418275A CH598758A5 (enExample) | 1974-04-03 | 1975-04-02 | |
| ZA00752044A ZA752044B (en) | 1974-04-03 | 1975-04-02 | Herbicide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2416139A DE2416139A1 (de) | 1974-04-03 | 1974-04-03 | Herbicide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2416139A1 true DE2416139A1 (de) | 1975-10-23 |
Family
ID=5912012
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2416139A Withdrawn DE2416139A1 (de) | 1974-04-03 | 1974-04-03 | Herbicide |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3972707A (enExample) |
| JP (1) | JPS5243887B2 (enExample) |
| AT (1) | AT340717B (enExample) |
| CA (1) | CA1041099A (enExample) |
| CH (1) | CH598758A5 (enExample) |
| DE (1) | DE2416139A1 (enExample) |
| ES (1) | ES436229A1 (enExample) |
| FR (1) | FR2266459A1 (enExample) |
| GB (1) | GB1478227A (enExample) |
| IL (1) | IL46984A (enExample) |
| NL (1) | NL7503091A (enExample) |
| ZA (1) | ZA752044B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0221439A1 (de) * | 1985-10-26 | 1987-05-13 | Hoechst Aktiengesellschaft | Herbizide Mittel, die stickstoffhaltige Heterocyclen mit Arylcarbamoyl-Resten enthalten, sowie neue heterocyclische Derivate mit Arylcarbamoyl-Resten |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4374991A (en) * | 1976-12-17 | 1983-02-22 | Rohm And Haas Company | 2,6-Dimethylpiperidinyl-N-carbobutoxymethyl urea |
| DE3601048A1 (de) * | 1986-01-16 | 1987-07-23 | Hoechst Ag | 1,2-disubstituierte piperidine, verfahren zu ihrer herstellung sowie ihre verwendung im pflanzenschutz |
| FR2669926A1 (fr) * | 1990-11-29 | 1992-06-05 | Medgenix Group Sa | Ligands specifiques des recepteurs aux benzodiazepines peripheriques. |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2053333A1 (de) * | 1970-10-30 | 1972-05-04 | Farbenfabriken Bayer Ag, 5090 Lever Kusen | Herbizide Mittel |
| JPS4825501B1 (enExample) * | 1970-12-29 | 1973-07-30 | ||
| JPS4935980B1 (enExample) * | 1971-06-30 | 1974-09-27 |
-
1974
- 1974-04-03 DE DE2416139A patent/DE2416139A1/de not_active Withdrawn
-
1975
- 1975-03-14 NL NL7503091A patent/NL7503091A/xx unknown
- 1975-03-20 GB GB1168775A patent/GB1478227A/en not_active Expired
- 1975-03-27 US US05/562,476 patent/US3972707A/en not_active Expired - Lifetime
- 1975-03-31 JP JP50039009A patent/JPS5243887B2/ja not_active Expired
- 1975-04-01 CA CA223,437A patent/CA1041099A/en not_active Expired
- 1975-04-01 IL IL46984A patent/IL46984A/en unknown
- 1975-04-02 ES ES436229A patent/ES436229A1/es not_active Expired
- 1975-04-02 AT AT249275A patent/AT340717B/de not_active IP Right Cessation
- 1975-04-02 FR FR7510236A patent/FR2266459A1/fr not_active Withdrawn
- 1975-04-02 CH CH418275A patent/CH598758A5/xx not_active IP Right Cessation
- 1975-04-02 ZA ZA00752044A patent/ZA752044B/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0221439A1 (de) * | 1985-10-26 | 1987-05-13 | Hoechst Aktiengesellschaft | Herbizide Mittel, die stickstoffhaltige Heterocyclen mit Arylcarbamoyl-Resten enthalten, sowie neue heterocyclische Derivate mit Arylcarbamoyl-Resten |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1478227A (en) | 1977-06-29 |
| FR2266459A1 (enExample) | 1975-10-31 |
| US3972707A (en) | 1976-08-03 |
| AT340717B (de) | 1977-12-27 |
| AU7933575A (en) | 1976-09-23 |
| IL46984A0 (en) | 1975-06-25 |
| NL7503091A (nl) | 1975-10-07 |
| ES436229A1 (es) | 1977-01-01 |
| CH598758A5 (enExample) | 1978-05-12 |
| ATA249275A (de) | 1977-04-15 |
| JPS50135230A (enExample) | 1975-10-27 |
| IL46984A (en) | 1977-12-30 |
| ZA752044B (en) | 1976-03-31 |
| JPS5243887B2 (enExample) | 1977-11-02 |
| CA1041099A (en) | 1978-10-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8141 | Disposal/no request for examination |