PL91502B1 - - Google Patents
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- Publication number
- PL91502B1 PL91502B1 PL1974173276A PL17327674A PL91502B1 PL 91502 B1 PL91502 B1 PL 91502B1 PL 1974173276 A PL1974173276 A PL 1974173276A PL 17327674 A PL17327674 A PL 17327674A PL 91502 B1 PL91502 B1 PL 91502B1
- Authority
- PL
- Poland
- Prior art keywords
- phenyl
- carbamoyloxy
- carbamate
- thiocarbamate
- methyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 16
- 230000002363 herbicidal effect Effects 0.000 claims description 13
- 239000004480 active ingredient Substances 0.000 claims description 11
- 239000004009 herbicide Substances 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- -1 alkyl radical Chemical class 0.000 description 27
- 241000196324 Embryophyta Species 0.000 description 21
- 239000003795 chemical substances by application Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000000969 carrier Substances 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 235000017060 Arachis glabrata Nutrition 0.000 description 3
- 244000105624 Arachis hypogaea Species 0.000 description 3
- 235000010777 Arachis hypogaea Nutrition 0.000 description 3
- 235000018262 Arachis monticola Nutrition 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 235000020232 peanut Nutrition 0.000 description 3
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 240000004385 Centaurea cyanus Species 0.000 description 2
- 235000005940 Centaurea cyanus Nutrition 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 244000299507 Gossypium hirsutum Species 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 240000003705 Senecio vulgaris Species 0.000 description 2
- 240000005498 Setaria italica Species 0.000 description 2
- 235000007226 Setaria italica Nutrition 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 240000006694 Stellaria media Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000009973 maize Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000007530 organic bases Chemical group 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- NDUPDOJHUQKPAG-UHFFFAOYSA-M 2,2-Dichloropropanoate Chemical compound CC(Cl)(Cl)C([O-])=O NDUPDOJHUQKPAG-UHFFFAOYSA-M 0.000 description 1
- GELMWIVBBPAMIO-UHFFFAOYSA-N 2-methylbutan-2-amine Chemical compound CCC(C)(C)N GELMWIVBBPAMIO-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical class O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- JSIAIROWMJGMQZ-UHFFFAOYSA-N 2h-triazol-4-amine Chemical class NC1=CNN=N1 JSIAIROWMJGMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 244000237956 Amaranthus retroflexus Species 0.000 description 1
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 1
- 235000007320 Avena fatua Nutrition 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- NQKVEJWLEDFCGQ-UHFFFAOYSA-N C(C)C(C#C)(CC)NC(=O)OC=1C=C(C=CC1)NC(OC(C)C)=O Chemical compound C(C)C(C#C)(CC)NC(=O)OC=1C=C(C=CC1)NC(OC(C)C)=O NQKVEJWLEDFCGQ-UHFFFAOYSA-N 0.000 description 1
- 244000144786 Chrysanthemum segetum Species 0.000 description 1
- 235000005470 Chrysanthemum segetum Nutrition 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 244000058871 Echinochloa crus-galli Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000303225 Lamium amplexicaule Species 0.000 description 1
- 235000009198 Lamium amplexicaule Nutrition 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- PGOAJNACWVUEHX-UHFFFAOYSA-N OC(=O)N(C)C1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 Chemical compound OC(=O)N(C)C1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 PGOAJNACWVUEHX-UHFFFAOYSA-N 0.000 description 1
- 235000011999 Panicum crusgalli Nutrition 0.000 description 1
- 240000006928 Persicaria lapathifolia Species 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 1
- 235000017016 Setaria faberi Nutrition 0.000 description 1
- 241001355178 Setaria faberi Species 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- JDODIRQZJXDLAP-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] carbonochloridate Chemical compound CCOC(=O)NC1=CC=CC(OC(Cl)=O)=C1 JDODIRQZJXDLAP-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 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
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 150000004891 diazines Chemical class 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 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
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 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
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 239000000725 suspension Substances 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
- 125000000101 thioether group Chemical group 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009736 wetting Methods 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 |
|---|---|---|---|
| DE2341079A DE2341079C2 (de) | 1973-08-10 | 1973-08-10 | m-Diurethane und selektive herbizide Mittel enthaltend diese Verbindungen als Wirkstoffe |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL91502B1 true PL91502B1 (en, 2012) | 1977-02-28 |
Family
ID=5889720
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1974173276A PL91502B1 (en, 2012) | 1973-08-10 | 1974-08-06 |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4252557A (en, 2012) |
| JP (1) | JPS5745408B2 (en, 2012) |
| AT (1) | AT335793B (en, 2012) |
| BE (1) | BE818693A (en, 2012) |
| BG (1) | BG21834A3 (en, 2012) |
| BR (1) | BR7406544D0 (en, 2012) |
| CA (1) | CA1056394A (en, 2012) |
| CH (1) | CH608168A5 (en, 2012) |
| CS (1) | CS174788B2 (en, 2012) |
| CU (1) | CU21100A (en, 2012) |
| DD (1) | DD113302A5 (en, 2012) |
| DE (1) | DE2341079C2 (en, 2012) |
| EG (1) | EG11374A (en, 2012) |
| ES (1) | ES428821A1 (en, 2012) |
| FR (1) | FR2240210B1 (en, 2012) |
| GB (1) | GB1483762A (en, 2012) |
| IL (1) | IL45440A (en, 2012) |
| IT (1) | IT1022072B (en, 2012) |
| NL (1) | NL7410748A (en, 2012) |
| PH (1) | PH11289A (en, 2012) |
| PL (1) | PL91502B1 (en, 2012) |
| RO (1) | RO70413A (en, 2012) |
| SU (2) | SU522768A3 (en, 2012) |
| YU (1) | YU36922B (en, 2012) |
| ZA (1) | ZA745123B (en, 2012) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5839126B2 (ja) * | 1976-08-11 | 1983-08-27 | クミアイ化学工業株式会社 | 除草用組成物 |
| GR78909B (en, 2012) * | 1982-08-13 | 1984-10-02 | Sipcam Spa | |
| ES8604495A1 (es) * | 1983-09-20 | 1986-02-01 | Koege Kemisk Vaerk | Un procedimiento para preparar fenil-carbamatos sustituidos |
| CZ280059B6 (cs) * | 1984-02-29 | 1995-10-18 | Schering Aktiengesellschaft | Stabilizovaný kapalný herbicidní prostředek a způsob hubení plevelných rostlin |
| US5246912A (en) * | 1984-02-29 | 1993-09-21 | Berol Nobel (Suisse) S.A. | Herbicidal compositions of phenmedipham and desmedipham |
| JPS611725U (ja) * | 1984-06-12 | 1986-01-08 | トヨタ自動車株式会社 | ゴムブツシユ |
| CA2482069C (en) | 2002-04-12 | 2011-06-14 | Siemens Aktiengesellschaft | Curved belt conveyor |
| RU2422481C1 (ru) * | 2009-11-18 | 2011-06-27 | Общество с ограниченной ответственностью "НПК "РосИзоПром" | Композиция для нанесения теплоизоляционного покрытия и способ ее приготовления |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3124446A (en) * | 1964-03-10 | Controlling the growth of undesirfid | ||
| US3404975A (en) * | 1964-12-18 | 1968-10-08 | Fmc Corp | m-(carbamoyloxy)-carbanilates as herbicides |
| US3558685A (en) * | 1967-03-09 | 1971-01-26 | Basf Ag | Substituted thiol carbamates |
| US3687997A (en) * | 1969-03-27 | 1972-08-29 | Karl Kiehs | Ethyl n-cyclohexyl n-propargyl-thiolcarbamate as a herbicide |
| US3746741A (en) * | 1969-10-27 | 1973-07-17 | Ciba Ltd | Phenoxyacetic acid derivatives |
| DE2109798C3 (de) * | 1971-02-23 | 1979-12-20 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | N-3-Carbamoyloxyphenyl-Thiolcarbamate sowie diese enthaltendes herbizides Mittel |
| US3792994A (en) * | 1972-12-26 | 1974-02-19 | Stauffer Chemical Co | Anilide carbamates as algicidal agents |
-
1973
- 1973-08-10 DE DE2341079A patent/DE2341079C2/de not_active Expired
-
1974
- 1974-07-16 YU YU1978/74A patent/YU36922B/xx unknown
- 1974-07-31 ES ES428821A patent/ES428821A1/es not_active Expired
- 1974-08-03 RO RO7479664A patent/RO70413A/ro unknown
- 1974-08-05 CS CS5550A patent/CS174788B2/cs unknown
- 1974-08-05 BG BG027429A patent/BG21834A3/xx unknown
- 1974-08-06 PL PL1974173276A patent/PL91502B1/pl unknown
- 1974-08-06 JP JP49090195A patent/JPS5745408B2/ja not_active Expired
- 1974-08-07 IT IT26099/74A patent/IT1022072B/it active
- 1974-08-08 BR BR6544/74A patent/BR7406544D0/pt unknown
- 1974-08-08 DD DD180403A patent/DD113302A5/xx unknown
- 1974-08-08 CH CH1083874A patent/CH608168A5/xx not_active IP Right Cessation
- 1974-08-08 AT AT650774A patent/AT335793B/de not_active IP Right Cessation
- 1974-08-09 SU SU2051196A patent/SU522768A3/ru active
- 1974-08-09 ZA ZA00745123A patent/ZA745123B/xx unknown
- 1974-08-09 IL IL45440A patent/IL45440A/xx unknown
- 1974-08-09 CU CU7434101A patent/CU21100A/es unknown
- 1974-08-09 FR FR7427705A patent/FR2240210B1/fr not_active Expired
- 1974-08-09 BE BE147473A patent/BE818693A/xx not_active IP Right Cessation
- 1974-08-09 NL NL7410748A patent/NL7410748A/xx not_active Application Discontinuation
- 1974-08-09 PH PH16156A patent/PH11289A/en unknown
- 1974-08-09 SU SU742053051A patent/SU615854A3/ru active
- 1974-08-10 EG EG323/74A patent/EG11374A/xx active
- 1974-08-12 GB GB35426/74A patent/GB1483762A/en not_active Expired
- 1974-08-12 CA CA206,817A patent/CA1056394A/en not_active Expired
-
1979
- 1979-06-11 US US06/047,126 patent/US4252557A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| IL45440A (en) | 1978-03-10 |
| JPS5745408B2 (en, 2012) | 1982-09-28 |
| RO70413A (ro) | 1980-06-15 |
| BR7406544D0 (pt) | 1975-05-27 |
| JPS5042034A (en, 2012) | 1975-04-16 |
| AU7225474A (en) | 1976-02-12 |
| US4252557A (en) | 1981-02-24 |
| PH11289A (en) | 1977-11-02 |
| ES428821A1 (es) | 1976-08-16 |
| NL7410748A (nl) | 1975-02-12 |
| YU36922B (en) | 1984-08-31 |
| ATA650774A (de) | 1976-07-15 |
| GB1483762A (en) | 1977-08-24 |
| FR2240210B1 (en, 2012) | 1978-11-24 |
| DD113302A5 (en, 2012) | 1975-06-05 |
| DE2341079A1 (de) | 1975-02-20 |
| IL45440A0 (en) | 1974-11-29 |
| SU522768A3 (ru) | 1976-07-25 |
| CS174788B2 (en, 2012) | 1977-04-29 |
| CH608168A5 (en, 2012) | 1978-12-29 |
| EG11374A (en) | 1977-12-31 |
| CU21100A (es) | 1981-09-09 |
| DE2341079C2 (de) | 1982-05-06 |
| SU615854A3 (ru) | 1978-07-15 |
| FR2240210A1 (en, 2012) | 1975-03-07 |
| ZA745123B (en) | 1975-09-24 |
| CA1056394A (en) | 1979-06-12 |
| YU197874A (en) | 1982-02-25 |
| BE818693A (fr) | 1975-02-10 |
| AT335793B (de) | 1977-03-25 |
| BG21834A3 (bg) | 1976-09-20 |
| IT1022072B (it) | 1978-03-20 |
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