DE2003143C3 - N-Arylharnstoffe, Verfahren zu ihrer Herstellung und diese enthaltende herbicide Mittel - Google Patents
N-Arylharnstoffe, Verfahren zu ihrer Herstellung und diese enthaltende herbicide MittelInfo
- Publication number
- DE2003143C3 DE2003143C3 DE2003143A DE2003143A DE2003143C3 DE 2003143 C3 DE2003143 C3 DE 2003143C3 DE 2003143 A DE2003143 A DE 2003143A DE 2003143 A DE2003143 A DE 2003143A DE 2003143 C3 DE2003143 C3 DE 2003143C3
- Authority
- DE
- Germany
- Prior art keywords
- active ingredient
- preparation
- arylureas
- processes
- 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.)
- Expired
Links
- 238000000034 method Methods 0.000 title description 6
- 238000002360 preparation method Methods 0.000 title description 6
- 239000004009 herbicide Substances 0.000 title description 4
- 210000002700 urine Anatomy 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 26
- 241000196324 Embryophyta Species 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 10
- 239000000460 chlorine Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 241000209140 Triticum Species 0.000 description 7
- 235000021307 Triticum Nutrition 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- -1 difluorochloromethylmercapto Chemical class 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 239000012948 isocyanate Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000002363 herbicidal effect Effects 0.000 description 5
- 244000075850 Avena orientalis Species 0.000 description 4
- 241000219312 Chenopodium Species 0.000 description 4
- 241000192043 Echinochloa Species 0.000 description 4
- 241000219146 Gossypium Species 0.000 description 4
- 241000220261 Sinapis Species 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 235000007319 Avena orientalis Nutrition 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241000209094 Oryza Species 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- 241000209200 Bromus Species 0.000 description 2
- 241000723377 Coffea Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 235000007351 Eleusine Nutrition 0.000 description 2
- 241000209215 Eleusine Species 0.000 description 2
- 241000234642 Festuca Species 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 241000209082 Lolium Species 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 240000006694 Stellaria media Species 0.000 description 2
- 241000219422 Urtica Species 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 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
- 239000000839 emulsion Substances 0.000 description 2
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000019713 millet Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 240000002245 Acer pensylvanicum Species 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000003130 Arctium lappa Nutrition 0.000 description 1
- 235000008078 Arctium minus Nutrition 0.000 description 1
- 235000005781 Avena Nutrition 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- 244000056139 Brassica cretica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 240000003538 Chamaemelum nobile 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
- 241000208175 Daucus Species 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- ZODJBSVGEFIIPJ-UHFFFAOYSA-N FCl(SC)(Cl)F Chemical compound FCl(SC)(Cl)F ZODJBSVGEFIIPJ-UHFFFAOYSA-N 0.000 description 1
- 241000748465 Galinsoga Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 235000009438 Gossypium Nutrition 0.000 description 1
- 206010053759 Growth retardation Diseases 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 241000801118 Lepidium Species 0.000 description 1
- 244000211187 Lepidium sativum Species 0.000 description 1
- 235000007849 Lepidium sativum Nutrition 0.000 description 1
- 241000209510 Liliopsida Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000209117 Panicum Species 0.000 description 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
- 241000219833 Phaseolus Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000746981 Phleum Species 0.000 description 1
- 241000746983 Phleum pratense Species 0.000 description 1
- 241001310793 Podium Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000209051 Saccharum Species 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000780602 Senecio Species 0.000 description 1
- 240000003705 Senecio vulgaris Species 0.000 description 1
- 235000005775 Setaria Nutrition 0.000 description 1
- 241000232088 Setaria <nematode> Species 0.000 description 1
- 235000002634 Solanum Nutrition 0.000 description 1
- 241000207763 Solanum Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000152045 Themeda triandra Species 0.000 description 1
- 244000274883 Urtica dioica Species 0.000 description 1
- 235000009108 Urtica dioica Nutrition 0.000 description 1
- 241000209149 Zea Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 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
- 239000004202 carbamide Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 244000230030 foxtail bristlegrass Species 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 231100000001 growth retardation Toxicity 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
- C07C323/43—Y being a hetero atom
- C07C323/44—X or Y being nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (16)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE757221D BE757221A (fr) | 1970-01-24 | Nouvelles n-arylurees, leur procede de preparation et leur application comme herbicides | |
| DE2003143A DE2003143C3 (de) | 1970-01-24 | 1970-01-24 | N-Arylharnstoffe, Verfahren zu ihrer Herstellung und diese enthaltende herbicide Mittel |
| GB4268270A GB1314864A (en) | 1970-01-24 | 1970-09-07 | N-arylureas a process for their production and their use as herbicid |
| IL35324A IL35324A (en) | 1970-01-24 | 1970-09-21 | N-difluorochloromethylthio-phenylureas,their production and their use as herbicides |
| NL7014009A NL7014009A (enExample) | 1970-01-24 | 1970-09-22 | |
| CH1409670A CH528488A (de) | 1970-01-24 | 1970-09-23 | Verfahren zur Herstellung von N-Arylharnstoffen |
| BG015704A BG17452A3 (bg) | 1970-01-24 | 1970-09-23 | Хербицидно средство |
| CS6531A CS161116B2 (enExample) | 1970-01-24 | 1970-09-25 | |
| ES384036A ES384036A1 (es) | 1970-01-24 | 1970-09-28 | Procedimiento para la obtencion de n-arilureas. |
| JP45084737A JPS4825491B1 (enExample) | 1970-01-24 | 1970-09-29 | |
| JP45084736A JPS4914745B1 (enExample) | 1970-01-24 | 1970-09-29 | |
| FR7036795A FR2074892A5 (enExample) | 1970-01-24 | 1970-10-12 | |
| RO64715A RO58949A (enExample) | 1970-01-24 | 1970-10-16 | |
| TR17120A TR17120A (tr) | 1970-01-24 | 1970-10-26 | N-aril uereler,bunlarin imaline mahsus usul ve bunlarin zarali bitki oeldueruecue madde olarak kullanilmalari |
| US05/356,261 US3931312A (en) | 1970-01-24 | 1973-05-01 | Novel N(-difluoromethylmercaptophenyl) urea compounds and herbicidal compositions |
| US05/606,982 US4039315A (en) | 1970-01-24 | 1975-08-22 | N-(Difluorochloromethylmercaptophenyl)ureas as herbicides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2003143A DE2003143C3 (de) | 1970-01-24 | 1970-01-24 | N-Arylharnstoffe, Verfahren zu ihrer Herstellung und diese enthaltende herbicide Mittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2003143A1 DE2003143A1 (de) | 1971-07-29 |
| DE2003143B2 DE2003143B2 (de) | 1973-10-04 |
| DE2003143C3 true DE2003143C3 (de) | 1974-05-16 |
Family
ID=5760406
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2003143A Expired DE2003143C3 (de) | 1970-01-24 | 1970-01-24 | N-Arylharnstoffe, Verfahren zu ihrer Herstellung und diese enthaltende herbicide Mittel |
Country Status (13)
| Country | Link |
|---|---|
| JP (2) | JPS4914745B1 (enExample) |
| BE (1) | BE757221A (enExample) |
| BG (1) | BG17452A3 (enExample) |
| CH (1) | CH528488A (enExample) |
| CS (1) | CS161116B2 (enExample) |
| DE (1) | DE2003143C3 (enExample) |
| ES (1) | ES384036A1 (enExample) |
| FR (1) | FR2074892A5 (enExample) |
| GB (1) | GB1314864A (enExample) |
| IL (1) | IL35324A (enExample) |
| NL (1) | NL7014009A (enExample) |
| RO (1) | RO58949A (enExample) |
| TR (1) | TR17120A (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2234586A1 (de) * | 1972-07-14 | 1974-01-31 | Bayer Ag | N-arylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
-
0
- BE BE757221D patent/BE757221A/xx unknown
-
1970
- 1970-01-24 DE DE2003143A patent/DE2003143C3/de not_active Expired
- 1970-09-07 GB GB4268270A patent/GB1314864A/en not_active Expired
- 1970-09-21 IL IL35324A patent/IL35324A/xx unknown
- 1970-09-22 NL NL7014009A patent/NL7014009A/xx unknown
- 1970-09-23 CH CH1409670A patent/CH528488A/de not_active IP Right Cessation
- 1970-09-23 BG BG015704A patent/BG17452A3/xx unknown
- 1970-09-25 CS CS6531A patent/CS161116B2/cs unknown
- 1970-09-28 ES ES384036A patent/ES384036A1/es not_active Expired
- 1970-09-29 JP JP45084736A patent/JPS4914745B1/ja active Pending
- 1970-09-29 JP JP45084737A patent/JPS4825491B1/ja active Pending
- 1970-10-12 FR FR7036795A patent/FR2074892A5/fr not_active Expired
- 1970-10-16 RO RO64715A patent/RO58949A/ro unknown
- 1970-10-26 TR TR17120A patent/TR17120A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2003143B2 (de) | 1973-10-04 |
| ES384036A1 (es) | 1972-12-16 |
| IL35324A (en) | 1974-03-14 |
| GB1314864A (en) | 1973-04-26 |
| BE757221A (fr) | 1971-04-08 |
| CH528488A (de) | 1972-09-30 |
| TR17120A (tr) | 1974-04-25 |
| JPS4825491B1 (enExample) | 1973-07-30 |
| JPS4914745B1 (enExample) | 1974-04-10 |
| BG17452A3 (bg) | 1973-11-10 |
| DE2003143A1 (de) | 1971-07-29 |
| NL7014009A (enExample) | 1971-07-27 |
| CS161116B2 (enExample) | 1975-05-04 |
| IL35324A0 (en) | 1970-11-30 |
| FR2074892A5 (enExample) | 1971-10-08 |
| RO58949A (enExample) | 1976-02-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| E77 | Valid patent as to the heymanns-index 1977 | ||
| EHV | Ceased/renunciation |