CS244845B2 - Agent for curtural plants protection andcproduction method of effective substances - Google Patents
Agent for curtural plants protection andcproduction method of effective substances Download PDFInfo
- Publication number
- CS244845B2 CS244845B2 CS849614A CS961484A CS244845B2 CS 244845 B2 CS244845 B2 CS 244845B2 CS 849614 A CS849614 A CS 849614A CS 961484 A CS961484 A CS 961484A CS 244845 B2 CS244845 B2 CS 244845B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- oder
- alkyl
- und
- group
- alkenyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 4
- 239000000126 substance Substances 0.000 title description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 5
- 150000002367 halogens Chemical class 0.000 claims abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 4
- 239000001301 oxygen Substances 0.000 claims abstract description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract 8
- 239000004009 herbicide Substances 0.000 claims description 12
- 230000002363 herbicidal effect Effects 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000013543 active substance Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000005557 antagonist Substances 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 2
- -1 chlorvinyl Chemical group 0.000 claims 13
- 125000000262 haloalkenyl group Chemical group 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000000460 chlorine Substances 0.000 claims 3
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims 3
- 125000001188 haloalkyl group Chemical group 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- 125000001478 1-chloroethyl group Chemical group [H]C([H])([H])C([H])(Cl)* 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 239000000543 intermediate Substances 0.000 claims 2
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims 2
- 125000000453 2,2,2-trichloroethyl group Chemical group [H]C([H])(*)C(Cl)(Cl)Cl 0.000 claims 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- KHOJDNRIFDLPQQ-UHFFFAOYSA-N 2-chloro-1-(3-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)propan-1-one Chemical compound C1=CC=C2N(C(=O)C(Cl)C)C(C)COC2=C1 KHOJDNRIFDLPQQ-UHFFFAOYSA-N 0.000 claims 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims 1
- KKZUMAMOMRDVKA-UHFFFAOYSA-N 2-chloropropane Chemical group [CH2]C(C)Cl KKZUMAMOMRDVKA-UHFFFAOYSA-N 0.000 claims 1
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims 1
- 229940035676 analgesics Drugs 0.000 claims 1
- 239000000730 antalgic agent Substances 0.000 claims 1
- 229940125681 anticonvulsant agent Drugs 0.000 claims 1
- 239000001961 anticonvulsive agent Substances 0.000 claims 1
- 239000000935 antidepressant agent Substances 0.000 claims 1
- 229940005513 antidepressants Drugs 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000006003 dichloroethyl group Chemical group 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 244000038559 crop plants Species 0.000 abstract description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical compound ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 abstract 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- 241000862632 Soja Species 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 5
- 239000000729 antidote Substances 0.000 description 4
- 230000009931 harmful effect Effects 0.000 description 4
- 229940075522 antidotes Drugs 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- FOYHNROGBXVLLX-UHFFFAOYSA-N 2,6-diethylaniline Chemical compound CCC1=CC=CC(CC)=C1N FOYHNROGBXVLLX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical class NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000008061 acetanilides Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- SOWBFZRMHSNYGE-UHFFFAOYSA-N oxamic acid Chemical class NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/10—1,4-Thiazines; Hydrogenated 1,4-thiazines
- C07D279/14—1,4-Thiazines; Hydrogenated 1,4-thiazines condensed with carbocyclic rings or ring systems
- C07D279/16—1,4-Thiazines; Hydrogenated 1,4-thiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Catching Or Destruction (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56046683A | 1983-12-12 | 1983-12-12 | |
| US06/560,465 US4618361A (en) | 1983-12-12 | 1983-12-12 | Acylamides and compositions for the protection of cultivated plants against the phytotoxic action of herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS244845B2 true CS244845B2 (en) | 1986-08-14 |
Family
ID=27072353
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS849614A CS244845B2 (en) | 1983-12-12 | 1984-12-11 | Agent for curtural plants protection andcproduction method of effective substances |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP0149974B1 (ro) |
| JP (1) | JPH064605B2 (ro) |
| AU (1) | AU573663B2 (ro) |
| BG (1) | BG46001A3 (ro) |
| BR (1) | BR8406337A (ro) |
| CA (1) | CA1243022A (ro) |
| CS (1) | CS244845B2 (ro) |
| DE (1) | DE3474092D1 (ro) |
| ES (1) | ES538464A0 (ro) |
| HU (1) | HU194843B (ro) |
| IL (1) | IL73773A (ro) |
| MX (1) | MX159669A (ro) |
| MY (1) | MY100274A (ro) |
| NZ (1) | NZ210514A (ro) |
| RO (1) | RO90808A (ro) |
| ZW (1) | ZW20184A1 (ro) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60245753A (ja) * | 1984-05-22 | 1985-12-05 | Nippon Mining Co Ltd | 高力高導電銅合金 |
| US5541148A (en) * | 1992-07-08 | 1996-07-30 | Ciba-Geigy Corporation | Selective safened herbicidal composition comprising 2-ethoxycarbonyl-3-(4,6-dimethoxypyrimidine-2-yl) oxy-pyridine and an acylsulfamoylphenyl-urea safener |
| ATE179571T1 (de) * | 1993-03-22 | 1999-05-15 | Novartis Erfind Verwalt Gmbh | Selektiv-herbizides mittel |
| WO1994026108A1 (en) * | 1993-05-10 | 1994-11-24 | Zeneca Limited | Safening pyridyloxyphenoxy propionic acid herbicides |
| EE9500018A (et) * | 1994-06-03 | 1995-12-15 | Ciba-Geigy Ag | Selektiivne herbitsiid ja meetod selle kasutamiseks |
| BRPI0509289A (pt) | 2004-03-27 | 2007-09-18 | Bayer Cropscience Gmbh | combinação de protetor-herbicida |
| EP1696268B1 (en) | 2005-02-28 | 2016-11-09 | FUJIFILM Corporation | Lithographic printing plate precursor |
| EP1836894A1 (de) | 2006-03-25 | 2007-09-26 | Bayer CropScience GmbH | Neue Sulfonamid-haltige feste Formulungen |
| US7741317B2 (en) * | 2005-10-21 | 2010-06-22 | Bristol-Myers Squibb Company | LXR modulators |
| DE102005057250A1 (de) | 2005-11-29 | 2007-06-06 | Bayer Cropscience Gmbh | Wirkstoffe zur Steigerung der Stressabwehr in Pflanzen gegenüber abiotischem Stress und Methoden zu ihrer Auffindung |
| DE102007012168A1 (de) | 2007-03-12 | 2008-09-18 | Bayer Cropscience Ag | 2-[Heteroarylalkyl-sulfonyl]-thiazol-Derivate und 2-[Heteroarylalkyl-sulfinyl]-thiazol-Derivate, Verfahren zu deren Herstellung, sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| EP2065374A1 (de) | 2007-11-30 | 2009-06-03 | Bayer CropScience AG | 2-(Benzyl- und 1H-pyrazol-4-ylmethyl)sulfinyl-Thiazol-Derivate als Herbizide und Pflanzenwachstumsregulatoren |
| EP2065373A1 (de) | 2007-11-30 | 2009-06-03 | Bayer CropScience AG | Chirale 3-(Benzylsulfinyl)-5,5-dimethyl-4,5-dihydroisoxazol-Derivate und 5,5-Dimethyl-3-[(1H-pyrazol-4-ylmethyl) sulfinyl]-4,5-dihydroisoxazol-Derivate, Verfahren zu deren Herstellung sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| CN115666246A (zh) * | 2020-06-02 | 2023-01-31 | 拜耳公司 | 基于取代的异噁唑啉甲酰胺和解草酮的选择性除草剂 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1595863C3 (de) * | 1966-08-11 | 1978-03-02 | Knoll Ag, 6700 Ludwigshafen | 4-Piperidinoacetyl-3,4-dihydro-(2H)-l,4-benioxazin und Verfahren zu dessen Herstellung |
| FR2310348A1 (fr) * | 1975-05-07 | 1976-12-03 | Ugine Kuhlmann | Nouveaux derives heterocycliques antidotes contre herbicides |
| BG30323A3 (en) * | 1978-06-28 | 1981-05-15 | Bayer Aktiengesellschaft | Method for obtaining of n- dichloracethyl- 1, 2, 3, 4- tetrahydro- hinaldine |
| DE3426564A1 (de) * | 1984-07-19 | 1986-01-30 | Bayer Ag, 5090 Leverkusen | Verwendung von 4h-1,4-benzothiazinen bei der prophylaxe und therapie von erkrankungen der atemwege, entzuendungen/rheuma, thromboembolischen erkrankungen, ischaemien und infarkten, herzrhythmusstoerungen, arteriosklerose und dermatosen, arzneimittel zu diesem zweck sowie wirkstoffe, die in diesen arzneimitteln enthalten sind |
-
1984
- 1984-12-03 MX MX5737A patent/MX159669A/es unknown
- 1984-12-06 DE DE8484810599T patent/DE3474092D1/de not_active Expired
- 1984-12-06 EP EP84810599A patent/EP0149974B1/de not_active Expired
- 1984-12-10 ZW ZW201/84A patent/ZW20184A1/xx unknown
- 1984-12-10 IL IL73773A patent/IL73773A/xx not_active IP Right Cessation
- 1984-12-10 BG BG067835A patent/BG46001A3/xx unknown
- 1984-12-10 CA CA000469673A patent/CA1243022A/en not_active Expired
- 1984-12-10 RO RO84116600A patent/RO90808A/ro unknown
- 1984-12-11 HU HU844604A patent/HU194843B/hu unknown
- 1984-12-11 BR BR8406337A patent/BR8406337A/pt not_active IP Right Cessation
- 1984-12-11 NZ NZ210514A patent/NZ210514A/en unknown
- 1984-12-11 ES ES538464A patent/ES538464A0/es active Granted
- 1984-12-11 CS CS849614A patent/CS244845B2/cs unknown
- 1984-12-11 AU AU36484/84A patent/AU573663B2/en not_active Expired
- 1984-12-12 JP JP59262667A patent/JPH064605B2/ja not_active Expired - Lifetime
-
1987
- 1987-08-21 MY MYPI87001410A patent/MY100274A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUT36809A (en) | 1985-10-28 |
| BR8406337A (pt) | 1985-10-08 |
| ES8601165A1 (es) | 1985-11-01 |
| AU3648484A (en) | 1985-06-20 |
| MY100274A (en) | 1990-07-28 |
| JPH064605B2 (ja) | 1994-01-19 |
| RO90808A (ro) | 1987-02-27 |
| NZ210514A (en) | 1988-05-30 |
| ZW20184A1 (en) | 1985-07-17 |
| JPS60146882A (ja) | 1985-08-02 |
| AU573663B2 (en) | 1988-06-16 |
| EP0149974A3 (en) | 1985-08-21 |
| IL73773A0 (en) | 1985-03-31 |
| MX159669A (es) | 1989-08-02 |
| ES538464A0 (es) | 1985-11-01 |
| EP0149974B1 (de) | 1988-09-21 |
| DE3474092D1 (en) | 1988-10-27 |
| BG46001A3 (en) | 1989-09-15 |
| IL73773A (en) | 1988-11-30 |
| CA1243022A (en) | 1988-10-11 |
| HU194843B (en) | 1988-03-28 |
| EP0149974A2 (de) | 1985-07-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CS244845B2 (en) | Agent for curtural plants protection andcproduction method of effective substances | |
| DE69431932T2 (de) | Oligopeptide mit fungizider Aktivität | |
| BG60083B2 (bg) | Пестицидно средство и метод за борба с вредители по растенията | |
| EP1101760A4 (en) | DI- OR TRI-FLUOROMETHANESULFONYL ANILIDE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND HERBICIDES CONTAINING THEM IN THE FORM OF ACTIVE INGREDIENTS | |
| DE3810080A1 (de) | Trisubstituierte 1,3,5-triazin-2,4,6-trione | |
| DE3528583C2 (ro) | ||
| DE3835576A1 (de) | 3,7-disubstituierte benzthiazolone | |
| CH640108A5 (de) | Unkrautvernichtungsmittel. | |
| EP0165572A2 (de) | Neue herbizid wirksame Sulfonylharnstoffe | |
| US4284426A (en) | 2-Chloro-4,5-disubstituted-thiazoles useful as herbicidal safeners | |
| DE2042300A1 (de) | Halogencarbonsäureanilide, ihre Herstellung und Verwendung als Herbizide | |
| ATE116803T1 (de) | Herbizide zusammensetzung enthaltend 2-chlor-3- phenoxy-6-nitroanilin und mindestens ein herbizid ausgewählt aus bromoxynil, ioxynil und deren derivaten. | |
| US3330642A (en) | Agricultural chemical concentrates | |
| DE2846625A1 (de) | M-anilidurethane | |
| EP0170906B1 (de) | Pflanzenschützende Mittel auf Basis von Oximestern | |
| CS231991B2 (en) | Herbceous agent and manufacturing process of active substances | |
| DE2024249A1 (en) | Herbicidal phenylureas prodn - from substd isocyanates or carbamic - acid chlorides with amines or alkylated hydroxylamines | |
| JPS6452704A (en) | Detoxifying compound for use together with herbicide, herbicidal detoxicant and manufacture | |
| DE4000624A1 (de) | Fungizide verwendung von trisubstituierten 1,3,5-triazin-2,4,6-trionen, neue trisubstituierte 1,3,5-triazin-2,4,6-trione und verfahren zu ihrer herstellung | |
| DD248953A5 (de) | Schaedlingsbekaempfungsmittel | |
| US3449405A (en) | 2-halo-3-methylphenyl n-methylcarbamates | |
| ATE16285T1 (de) | Herbizide gegenmittel, deren herstellung, verwendung und zusammensetzung. | |
| DE3933933A1 (de) | Trisubstituierte 1,3,5-triazin-2,4,6-trione | |
| DD298392A5 (de) | Fungizide mittel auf basis von 1,3,5-triaryl-2-pyrazolin-derivaten, neue 1,3,5-triaryl-2-pyrazoline und ein verfahren zu ihrer herstellung | |
| US3238035A (en) | Herbicidal use of n-cycloalkyl-n-bis(beta-chloroalkyl)amines |