DE1643731A1 - Harnstoffderivate - Google Patents
HarnstoffderivateInfo
- Publication number
- DE1643731A1 DE1643731A1 DE19681643731 DE1643731A DE1643731A1 DE 1643731 A1 DE1643731 A1 DE 1643731A1 DE 19681643731 DE19681643731 DE 19681643731 DE 1643731 A DE1643731 A DE 1643731A DE 1643731 A1 DE1643731 A1 DE 1643731A1
- Authority
- DE
- Germany
- Prior art keywords
- trifluoromethylphenyl
- weight
- parts
- hydroxy
- methylurea
- 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.)
- Pending
Links
- 150000003672 ureas Chemical class 0.000 title claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000004009 herbicide Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 230000002363 herbicidal effect Effects 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 8
- 244000292693 Poa annua Species 0.000 description 7
- 235000009108 Urtica dioica Nutrition 0.000 description 7
- BNAKQHHDQJMEJF-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-hydroxy-3-methylurea Chemical compound CNC(=O)N(O)C1=CC=C(Cl)C=C1 BNAKQHHDQJMEJF-UHFFFAOYSA-N 0.000 description 6
- MZOUVYBSKNDVCW-UHFFFAOYSA-N 1-hydroxy-3-methyl-1-[3-(trifluoromethyl)phenyl]urea Chemical compound CNC(=O)N(O)C1=CC=CC(C(F)(F)F)=C1 MZOUVYBSKNDVCW-UHFFFAOYSA-N 0.000 description 6
- 244000024671 Brassica kaber Species 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 240000005979 Hordeum vulgare Species 0.000 description 6
- 235000007340 Hordeum vulgare Nutrition 0.000 description 6
- 240000007594 Oryza sativa Species 0.000 description 6
- 235000007164 Oryza sativa Nutrition 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 244000098338 Triticum aestivum Species 0.000 description 6
- 244000274883 Urtica dioica Species 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 description 5
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 4
- 244000062793 Sorghum vulgare Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 235000019713 millet Nutrition 0.000 description 4
- 235000009566 rice Nutrition 0.000 description 4
- -1 3- (3'-trifluoromethylphenyl) -3-hydroxy-1,1-dimethylurea Chemical compound 0.000 description 3
- 235000008427 Brassica arvensis Nutrition 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 240000006694 Stellaria media Species 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- BTBCKFKJZWXNSB-UHFFFAOYSA-N n-[3-(trifluoromethyl)phenyl]hydroxylamine Chemical compound ONC1=CC=CC(C(F)(F)F)=C1 BTBCKFKJZWXNSB-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 235000007320 Avena fatua Nutrition 0.000 description 2
- 241000209764 Avena fatua Species 0.000 description 2
- 235000005637 Brassica campestris Nutrition 0.000 description 2
- 235000014750 Brassica kaber Nutrition 0.000 description 2
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 2
- 235000010570 Brassica rapa var. rapa Nutrition 0.000 description 2
- XCBSVLCHDLISJB-UHFFFAOYSA-N CNC(N(C1=CC(C(F)(F)F)=CC=C1)OC)=O Chemical compound CNC(N(C1=CC(C(F)(F)F)=CC=C1)OC)=O XCBSVLCHDLISJB-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000009973 maize Nutrition 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229920005552 sodium lignosulfonate Polymers 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 210000002700 urine Anatomy 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- WHNAMGUAXHGCHH-UHFFFAOYSA-N 1-nitro-3-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC=CC(C(F)(F)F)=C1 WHNAMGUAXHGCHH-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- VKTTYIXIDXWHKW-UHFFFAOYSA-N 2-chloro-5-(trifluoromethyl)aniline Chemical compound NC1=CC(C(F)(F)F)=CC=C1Cl VKTTYIXIDXWHKW-UHFFFAOYSA-N 0.000 description 1
- VIUDTWATMPPKEL-UHFFFAOYSA-N 3-(trifluoromethyl)aniline Chemical compound NC1=CC=CC(C(F)(F)F)=C1 VIUDTWATMPPKEL-UHFFFAOYSA-N 0.000 description 1
- 241000209761 Avena Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000011292 Brassica rapa Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241001456088 Hesperocnide Species 0.000 description 1
- VSNHCAURESNICA-UHFFFAOYSA-N Hydroxyurea Chemical class NC(=O)NO VSNHCAURESNICA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- CKRZKMFTZCFYGB-UHFFFAOYSA-N N-phenylhydroxylamine Chemical class ONC1=CC=CC=C1 CKRZKMFTZCFYGB-UHFFFAOYSA-N 0.000 description 1
- 244000088461 Panicum crus-galli Species 0.000 description 1
- 235000011999 Panicum crusgalli Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 240000003461 Setaria viridis Species 0.000 description 1
- 235000002248 Setaria viridis Nutrition 0.000 description 1
- 235000007244 Zea mays Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002540 isothiocyanates Chemical class 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000005181 nitrobenzenes Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/64—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups singly-bound to oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681643731 DE1643731A1 (de) | 1968-01-05 | 1968-01-05 | Harnstoffderivate |
| GB55269A GB1242332A (en) | 1968-01-05 | 1969-01-03 | Urea derivatives |
| AT5769A AT286706B (de) | 1968-01-05 | 1969-01-03 | Herbizid |
| BE726472D BE726472A (enrdf_load_stackoverflow) | 1968-01-05 | 1969-01-03 | |
| NL6900116A NL6900116A (enrdf_load_stackoverflow) | 1968-01-05 | 1969-01-03 | |
| CH6369A CH505549A (de) | 1968-01-05 | 1969-01-06 | Herbizid, Verfahren zu seiner Herstellung und seine Verwendung zum Bekämpfen unerwünschten Pflanzenwachstums |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681643731 DE1643731A1 (de) | 1968-01-05 | 1968-01-05 | Harnstoffderivate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1643731A1 true DE1643731A1 (de) | 1971-06-24 |
Family
ID=5684379
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19681643731 Pending DE1643731A1 (de) | 1968-01-05 | 1968-01-05 | Harnstoffderivate |
Country Status (6)
| Country | Link |
|---|---|
| AT (1) | AT286706B (enrdf_load_stackoverflow) |
| BE (1) | BE726472A (enrdf_load_stackoverflow) |
| CH (1) | CH505549A (enrdf_load_stackoverflow) |
| DE (1) | DE1643731A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1242332A (enrdf_load_stackoverflow) |
| NL (1) | NL6900116A (enrdf_load_stackoverflow) |
-
1968
- 1968-01-05 DE DE19681643731 patent/DE1643731A1/de active Pending
-
1969
- 1969-01-03 BE BE726472D patent/BE726472A/xx unknown
- 1969-01-03 GB GB55269A patent/GB1242332A/en not_active Expired
- 1969-01-03 AT AT5769A patent/AT286706B/de not_active IP Right Cessation
- 1969-01-03 NL NL6900116A patent/NL6900116A/xx unknown
- 1969-01-06 CH CH6369A patent/CH505549A/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CH505549A (de) | 1971-04-15 |
| GB1242332A (en) | 1971-08-11 |
| BE726472A (enrdf_load_stackoverflow) | 1969-07-03 |
| NL6900116A (enrdf_load_stackoverflow) | 1969-07-08 |
| AT286706B (de) | 1970-12-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE3037105C2 (de) | Oxazolidon- und Thiazolidon-Derivate, Verfahren zu deren Herstellung und ihre Verwendung | |
| DE1915387A1 (de) | Herbizid | |
| DE1518815A1 (de) | Herbizid und Verfahren zu dessen Herstellung | |
| DE1670786A1 (de) | Biozide Praeparate | |
| DE3123018A1 (de) | Substituierte cyclohexan-1,3-dion-derivate, verfahren zu deren herstellung und herbicide mittel | |
| EP0028829A1 (de) | Harnstoffe mit cyclischen Substituenten, ihre Herstellung und Verwendung als Herbizide | |
| DE2339217A1 (de) | Neue cyclische verbindungen mit einer harnstoffgruppe, verfahren zur herstellung und herbicide zusammensetzungen | |
| DE1542711C3 (de) | N Phenyl N5 oxyalkyl NP alkylharnstof fe, ihre Verwendung als Herbizide und diese enthaltende herbizide Mittel | |
| DE2210540C2 (de) | Cyanphenylcarbonate, Verfahren zu deren Herstellung sowie diese enthaltende herbizide Mittel | |
| DE2436108A1 (de) | Substituierte phenylharnstoffe, verfahren zu ihrer herstellung und herbizide mittel | |
| DE2706700A1 (de) | Verfahren zur herstellung von pyridazin-3-on-verbindungen, neue pyridazin-3-one und deren verwendung | |
| DE1643731A1 (de) | Harnstoffderivate | |
| DE2044735A1 (de) | Schädlingsbekämpfungsmittel | |
| DE2411320A1 (de) | (trifluormethylphenoxy)-phenylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide | |
| DE2017498A1 (de) | Neue Pyridylharnstoffe, ihre Herstellung und ihre Verwendung als Wirkstoffe in Schädlingsbekämpfungsmitteln | |
| DE1643719A1 (de) | Substitutierte Dinitroaniline und diese enthaltende Herbizide | |
| DE1027930B (de) | Mittel zur Bekaempfung unerwuenschten Pflanzenwuchses | |
| DE1542835A1 (de) | Herbizide Mittel | |
| DE2121957B2 (de) | Diurethane sowie diese enthaltende herbizide Mittel | |
| DE2129773A1 (de) | Substituierte N-(3-Aminocarbonyloxyphenyl)-N'-methylharnstoffe | |
| DE1642217A1 (de) | Herbizide | |
| DE2114774C3 (de) | m-(Halogenalkenyloxy)-phenyIharnstoffe, Verfahren zu ihrer Herstellung und sie enthaltende herbizide Mittel | |
| DE1542817A1 (de) | Herbizid | |
| DE2163381A1 (de) | Herbizide Komposition | |
| DE1953357A1 (de) | Cyclopropan-carbonsaeure-benzthiazylamide,Verfahren zu ihrer Herstellung sowie ihre Verwendung als Herbizide |