NO131151B - - Google Patents
Download PDFInfo
- Publication number
- NO131151B NO131151B NO4303/71A NO430371A NO131151B NO 131151 B NO131151 B NO 131151B NO 4303/71 A NO4303/71 A NO 4303/71A NO 430371 A NO430371 A NO 430371A NO 131151 B NO131151 B NO 131151B
- Authority
- NO
- Norway
- Prior art keywords
- methyl
- phenyl
- thiocarbamate
- compound
- solution
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 12
- 230000000694 effects Effects 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 6
- 239000004009 herbicide Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 230000002363 herbicidal effect Effects 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000013543 active substance Substances 0.000 description 15
- 241000196324 Embryophyta Species 0.000 description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- 244000025254 Cannabis sativa Species 0.000 description 8
- -1 carbamoyloxyphenylthiocarbamates Chemical class 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 6
- 150000007530 organic bases Chemical class 0.000 description 5
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 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
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 244000062793 Sorghum vulgare Species 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 150000007529 inorganic bases Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical class OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- YHWQJTNMKZWBBN-UHFFFAOYSA-N 4-ethyl-n-methylaniline Chemical compound CCC1=CC=C(NC)C=C1 YHWQJTNMKZWBBN-UHFFFAOYSA-N 0.000 description 1
- 125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 240000004385 Centaurea cyanus Species 0.000 description 1
- 235000005940 Centaurea cyanus Nutrition 0.000 description 1
- 240000006122 Chenopodium album Species 0.000 description 1
- 235000009344 Chenopodium album Nutrition 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 244000152970 Digitaria sanguinalis Species 0.000 description 1
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 244000214240 Galinsoga parviflora Species 0.000 description 1
- 235000018914 Galinsoga parviflora Nutrition 0.000 description 1
- 241000520028 Lamium Species 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 240000003705 Senecio vulgaris Species 0.000 description 1
- 240000005498 Setaria italica Species 0.000 description 1
- 235000007226 Setaria italica Nutrition 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- NXGJISZVWPEFPV-UHFFFAOYSA-N [3-(methylsulfanylcarbonylamino)phenyl] carbonochloridate Chemical compound CSC(=O)NC1=CC=CC(OC(Cl)=O)=C1 NXGJISZVWPEFPV-UHFFFAOYSA-N 0.000 description 1
- DXNQLZJOTVNBOZ-UHFFFAOYSA-N [O]C(=O)Nc1ccccc1 Chemical group [O]C(=O)Nc1ccccc1 DXNQLZJOTVNBOZ-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000004571 lime Substances 0.000 description 1
- 210000001699 lower leg Anatomy 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- CPGWSLFYXMRNDV-UHFFFAOYSA-N n-methyl-n-phenylcarbamoyl chloride Chemical compound ClC(=O)N(C)C1=CC=CC=C1 CPGWSLFYXMRNDV-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- BMBJSXKEXRFGAV-UHFFFAOYSA-N phenylcarbamothioic s-acid Chemical class SC(=O)NC1=CC=CC=C1 BMBJSXKEXRFGAV-UHFFFAOYSA-N 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- FZMQIVKTRXXFDS-UHFFFAOYSA-N s-methyl n-(3-hydroxyphenyl)carbamothioate Chemical compound CSC(=O)NC1=CC=CC(O)=C1 FZMQIVKTRXXFDS-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (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 |
---|---|---|---|
DE19702059309 DE2059309A1 (de) | 1970-11-24 | 1970-11-24 | Selektives herbizides Mittel |
Publications (2)
Publication Number | Publication Date |
---|---|
NO131151B true NO131151B (xx) | 1975-01-06 |
NO131151C NO131151C (xx) | 1975-04-16 |
Family
ID=5789776
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO4303/71A NO131151C (xx) | 1970-11-24 | 1971-11-23 |
Country Status (29)
Country | Link |
---|---|
JP (1) | JPS5015847B1 (xx) |
AT (1) | AT311717B (xx) |
AU (1) | AU461419B2 (xx) |
BE (1) | BE775754A (xx) |
BG (1) | BG20071A3 (xx) |
BR (1) | BR7105564D0 (xx) |
CA (1) | CA946408A (xx) |
CH (1) | CH561009A5 (xx) |
CS (1) | CS167323B2 (xx) |
DE (1) | DE2059309A1 (xx) |
DK (1) | DK128552B (xx) |
EG (1) | EG10238A (xx) |
ES (1) | ES393926A1 (xx) |
FI (1) | FI54219C (xx) |
FR (1) | FR2115339B1 (xx) |
GB (1) | GB1369491A (xx) |
HU (1) | HU163629B (xx) |
IE (1) | IE35674B1 (xx) |
IL (2) | IL38183A0 (xx) |
IT (1) | IT941776B (xx) |
LU (1) | LU64313A1 (xx) |
NL (1) | NL7116114A (xx) |
NO (1) | NO131151C (xx) |
OA (1) | OA03840A (xx) |
PH (1) | PH11826A (xx) |
PL (1) | PL81438B1 (xx) |
RO (2) | RO62664A2 (xx) |
YU (1) | YU35351B (xx) |
ZA (1) | ZA715706B (xx) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2310649C3 (de) * | 1973-03-01 | 1982-05-06 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Diurethane sowie diese enthaltende selektive herbizide Mittel |
-
1970
- 1970-11-24 DE DE19702059309 patent/DE2059309A1/de not_active Withdrawn
-
1971
- 1971-06-18 DK DK301571AA patent/DK128552B/da not_active IP Right Cessation
- 1971-06-25 YU YU1660/71A patent/YU35351B/xx unknown
- 1971-07-20 FI FI2057/71A patent/FI54219C/fi active
- 1971-07-28 CS CS5527A patent/CS167323B2/cs unknown
- 1971-08-05 ES ES393926A patent/ES393926A1/es not_active Expired
- 1971-08-11 PH PH12743A patent/PH11826A/en unknown
- 1971-08-16 BG BG018353A patent/BG20071A3/xx unknown
- 1971-08-25 BR BR5564/71A patent/BR7105564D0/pt unknown
- 1971-08-26 ZA ZA715706A patent/ZA715706B/xx unknown
- 1971-09-27 GB GB4494571A patent/GB1369491A/en not_active Expired
- 1971-09-28 IE IE1210/71A patent/IE35674B1/xx unknown
- 1971-09-30 CA CA124,101A patent/CA946408A/en not_active Expired
- 1971-10-01 RO RO76243A patent/RO62664A2/ro unknown
- 1971-10-01 RO RO68336A patent/RO62289A2/ro unknown
- 1971-11-15 EG EG498/71A patent/EG10238A/xx active
- 1971-11-15 AU AU35714/71A patent/AU461419B2/en not_active Expired
- 1971-11-19 IL IL38183A patent/IL38183A0/xx unknown
- 1971-11-22 PL PL1971151698A patent/PL81438B1/pl unknown
- 1971-11-22 LU LU64313D patent/LU64313A1/xx unknown
- 1971-11-22 CH CH1697271A patent/CH561009A5/xx not_active IP Right Cessation
- 1971-11-23 OA OA54416A patent/OA03840A/xx unknown
- 1971-11-23 NL NL7116114A patent/NL7116114A/xx not_active Application Discontinuation
- 1971-11-23 FR FR7141818A patent/FR2115339B1/fr not_active Expired
- 1971-11-23 NO NO4303/71A patent/NO131151C/no unknown
- 1971-11-23 AT AT1007871A patent/AT311717B/de not_active IP Right Cessation
- 1971-11-23 HU HUSCHE364*1A patent/HU163629B/hu unknown
- 1971-11-24 IT IT31542/71A patent/IT941776B/it active
- 1971-11-24 BE BE775754A patent/BE775754A/xx not_active IP Right Cessation
- 1971-11-24 JP JP46094400A patent/JPS5015847B1/ja active Pending
-
1974
- 1974-11-19 IL IL38183A patent/IL38183A/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE69932628T2 (de) | Herbizide | |
US5324854A (en) | Intermediate isocyana to benzenesulfonamide compounds | |
SI9300627A (en) | Selective herbicid comprising pyridinsulphonylureas and sulphamoylphenylureas | |
US4149872A (en) | N-pyridinyl urea and cyclopropanecarboxamide herbicides | |
JPS62292773A (ja) | トリ置換された1,3,5−トリアジン−2,4,6−トリオン類 | |
DE69126836T2 (de) | Herbizide | |
JPS59212490A (ja) | 縮合したn−フエニルスルホニル−n′−ピリミジニル尿素及びn−フエニルスルホニル−n′−トリアジニル尿素、その製法、中間体、組成物及び使用法 | |
JPH04235984A (ja) | 新規なスルホニル尿素 | |
US3535101A (en) | Herbicide and algicide means | |
EP0103537A2 (de) | N-Arylsulfonyl-N'-triazolylharnstoffe | |
EP0136455A1 (de) | Substituierte Phenylsulfonylguanidin-Derivate | |
NO176714B (no) | Herbicide [[(1,3,5-triazin-2-yl)aminokarbonylÅ-aminosulfonylÅbenzosyreestere og herbicid middel, og anvendelse av disse | |
NO131151B (xx) | ||
NO157025B (no) | Fremgangsmte for fremstilling av zr eller hf ved elektrolyse samt celle for gjennomfring av fremgangsmten. | |
KR910006988B1 (ko) | 2-알콕시아미노설포닐벤젠-설포닐우레아의 제조방법 | |
EP0057367B1 (de) | 2-Pyridyloxyacetanilid-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung | |
EP0062254A1 (de) | Substituierte Acetanilide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide | |
US3512955A (en) | Method of protecting plant growth | |
US3687998A (en) | Aliphatic sulfonoxyphenylureas | |
EP0148498A1 (de) | Neue Sulfonylguanidin-Derivate | |
CN112661704B (zh) | 单嘧磺隆衍生物及其制备方法、除草剂和除草方法 | |
CS208667B2 (en) | Herbicide means and method of making the active substances | |
RU2776177C1 (ru) | Производное тиофенкарбоксамида и средство для контроля заболевания растений, содержащее его | |
JPH04210971A (ja) | 置換β−ピリミジニルオキシ(チオ)−およびβ−トリアジニルオキシ(チオ)−シクロアルキルカルボン酸誘導体、その製造方法、これを含有する除草、殺虫および植物生長調整効果のある薬剤およびその薬剤の製造方法 | |
KR820001301B1 (ko) | 디우레탄 화합물의 제조방법 |