NO126458B - - Google Patents
Download PDFInfo
- Publication number
- NO126458B NO126458B NO1455/71A NO145571A NO126458B NO 126458 B NO126458 B NO 126458B NO 1455/71 A NO1455/71 A NO 1455/71A NO 145571 A NO145571 A NO 145571A NO 126458 B NO126458 B NO 126458B
- Authority
- NO
- Norway
- Prior art keywords
- phenyl
- carbamate
- mixtures
- carbamoyloxy
- methyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 29
- 230000002363 herbicidal effect Effects 0.000 claims description 13
- 239000004009 herbicide Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 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
- MVEFZZKZBYQFPP-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] n-(3-methylphenyl)carbamate Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 MVEFZZKZBYQFPP-UHFFFAOYSA-N 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 25
- 230000000694 effects Effects 0.000 description 15
- 239000013543 active substance Substances 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 6
- -1 chalk Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 235000021537 Beetroot Nutrition 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 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
- 240000005702 Galium aparine Species 0.000 description 2
- 244000042664 Matricaria chamomilla Species 0.000 description 2
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 2
- 235000021536 Sugar beet Nutrition 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- NXNKURIKNWLWKB-UHFFFAOYSA-N carbamoyloxy(phenyl)carbamic acid Chemical class NC(=O)ON(C(O)=O)C1=CC=CC=C1 NXNKURIKNWLWKB-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000003977 halocarboxylic acids Chemical class 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- XLPYYBNLEUOIMD-UHFFFAOYSA-N (2-carbamoyloxyphenyl) carbamate Chemical class NC(=O)OC1=CC=CC=C1OC(N)=O XLPYYBNLEUOIMD-UHFFFAOYSA-N 0.000 description 1
- BIVURTHHVREOQA-UHFFFAOYSA-N (3-carbamoyloxyphenyl)carbamic acid Chemical class NC(=O)OC1=CC=CC(NC(O)=O)=C1 BIVURTHHVREOQA-UHFFFAOYSA-N 0.000 description 1
- NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 description 1
- ZRRCPKLWTBJUHI-UHFFFAOYSA-N 1-[(2,3,6-trichlorophenyl)methoxy]propan-1-ol Chemical compound CCC(O)OCC1=C(Cl)C=CC(Cl)=C1Cl ZRRCPKLWTBJUHI-UHFFFAOYSA-N 0.000 description 1
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound 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
- NDUPDOJHUQKPAG-UHFFFAOYSA-M 2,2-Dichloropropanoate Chemical compound CC(Cl)(Cl)C([O-])=O NDUPDOJHUQKPAG-UHFFFAOYSA-M 0.000 description 1
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- JSIAIROWMJGMQZ-UHFFFAOYSA-N 2h-triazol-4-amine Chemical class NC1=CNN=N1 JSIAIROWMJGMQZ-UHFFFAOYSA-N 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
- 241000335053 Beta vulgaris Species 0.000 description 1
- 235000011293 Brassica napus Nutrition 0.000 description 1
- 240000008100 Brassica rapa Species 0.000 description 1
- 235000000540 Brassica rapa subsp rapa 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
- PXRROZVNOOEPPZ-UHFFFAOYSA-N Flupropanate Chemical compound OC(=O)C(F)(F)C(F)F PXRROZVNOOEPPZ-UHFFFAOYSA-N 0.000 description 1
- 235000016623 Fragaria vesca Nutrition 0.000 description 1
- 240000009088 Fragaria x ananassa Species 0.000 description 1
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 1
- 235000014820 Galium aparine Nutrition 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 244000303225 Lamium amplexicaule Species 0.000 description 1
- 235000009198 Lamium amplexicaule Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 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
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- MLNOEQVEPIITAK-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] n-phenylcarbamate Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=CC=CC=2)=C1 MLNOEQVEPIITAK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 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
- 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
- 150000001559 benzoic acids Chemical class 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 150000004891 diazines Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 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
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 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
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 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
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003560 thiocarbamic acids Chemical class 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003672 ureas 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
-
- 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
- A01N47/20—N-Aryl derivatives thereof
-
- 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2020729A DE2020729C2 (de) | 1970-04-23 | 1970-04-23 | Herbizide Mittel auf Basis von N-(3-(N'-Aryl-carbamoyloxy)-phenyl)-carbamaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO126458B true NO126458B (nl) | 1973-02-12 |
Family
ID=5769631
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO1455/71A NO126458B (nl) | 1970-04-23 | 1971-04-20 |
Country Status (30)
| Country | Link |
|---|---|
| JP (1) | JPS56402B1 (nl) |
| AT (1) | AT309881B (nl) |
| BE (1) | BE766206A (nl) |
| BG (1) | BG17708A3 (nl) |
| BR (1) | BR7101940D0 (nl) |
| CA (1) | CA962081A (nl) |
| CH (1) | CH557637A (nl) |
| CS (1) | CS167914B2 (nl) |
| CY (1) | CY805A (nl) |
| DE (1) | DE2020729C2 (nl) |
| DK (1) | DK127363B (nl) |
| EG (1) | EG10081A (nl) |
| FI (1) | FI52421C (nl) |
| FR (1) | FR2086280B1 (nl) |
| GB (1) | GB1350264A (nl) |
| HU (1) | HU162895B (nl) |
| IE (1) | IE35120B1 (nl) |
| IL (1) | IL36647A (nl) |
| KE (1) | KE2535A (nl) |
| LU (1) | LU62709A1 (nl) |
| MY (1) | MY7500132A (nl) |
| NL (1) | NL170088C (nl) |
| NO (1) | NO126458B (nl) |
| OA (1) | OA03621A (nl) |
| PH (1) | PH9730A (nl) |
| PL (1) | PL88965B3 (nl) |
| RO (1) | RO58295A (nl) |
| SE (1) | SE376150B (nl) |
| TR (1) | TR20883A (nl) |
| ZA (1) | ZA711634B (nl) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2413933A1 (de) * | 1974-03-20 | 1975-09-25 | Schering Ag | Diurethane mit selektiver herbizider wirkung |
| ES8604495A1 (es) * | 1983-09-20 | 1986-02-01 | Koege Kemisk Vaerk | Un procedimiento para preparar fenil-carbamatos sustituidos |
| SK278523B6 (en) * | 1984-02-29 | 1997-08-06 | Erik Nielsen | A stabilised liquid herbicidal agent and method for killing weed plants |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3404975A (en) * | 1964-12-18 | 1968-10-08 | Fmc Corp | m-(carbamoyloxy)-carbanilates as herbicides |
| DE1567151C3 (de) * | 1965-04-09 | 1974-02-21 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Diurethane, Verfahren zur Herstellung dieser Verbindungen sowie diese enthaltende herbizide Mittel |
| FR1536033A (fr) * | 1966-09-07 | 1968-08-09 | Schering Ag | Esters carbamiques et produits herbicides et algicides qui en contiennent |
| FR1536108A (fr) * | 1966-09-10 | 1968-08-09 | Schering Ag | Agents herbicides contenant des esters carbamiques |
-
1970
- 1970-04-23 DE DE2020729A patent/DE2020729C2/de not_active Expired
-
1971
- 1971-02-03 RO RO65792A patent/RO58295A/ro unknown
- 1971-02-10 TR TR20883A patent/TR20883A/xx unknown
- 1971-02-23 FI FI710513A patent/FI52421C/fi active
- 1971-02-26 CS CS1492A patent/CS167914B2/cs unknown
- 1971-03-03 LU LU62709D patent/LU62709A1/xx unknown
- 1971-03-04 BG BG016966A patent/BG17708A3/xx unknown
- 1971-03-12 ZA ZA711634A patent/ZA711634B/xx unknown
- 1971-03-13 EG EG112/71A patent/EG10081A/xx active
- 1971-03-20 OA OA54205A patent/OA03621A/xx unknown
- 1971-03-23 DK DK140471AA patent/DK127363B/da not_active IP Right Cessation
- 1971-03-30 IE IE406/71A patent/IE35120B1/xx unknown
- 1971-03-31 BR BR1940/71A patent/BR7101940D0/pt unknown
- 1971-04-05 CA CA109,616A patent/CA962081A/en not_active Expired
- 1971-04-14 SE SE7104829A patent/SE376150B/xx unknown
- 1971-04-14 AT AT314971A patent/AT309881B/de active
- 1971-04-19 CY CY805A patent/CY805A/xx unknown
- 1971-04-19 IL IL36647A patent/IL36647A/xx unknown
- 1971-04-19 GB GB2562671*A patent/GB1350264A/en not_active Expired
- 1971-04-19 PH PH12379*UA patent/PH9730A/en unknown
- 1971-04-20 NO NO1455/71A patent/NO126458B/no unknown
- 1971-04-21 PL PL1971147652A patent/PL88965B3/pl unknown
- 1971-04-22 HU HUSC328A patent/HU162895B/hu unknown
- 1971-04-22 FR FR7114356A patent/FR2086280B1/fr not_active Expired
- 1971-04-23 NL NLAANVRAGE7105589,A patent/NL170088C/nl not_active IP Right Cessation
- 1971-04-23 BE BE766206A patent/BE766206A/xx not_active IP Right Cessation
- 1971-04-23 JP JP2663471A patent/JPS56402B1/ja active Pending
- 1971-04-23 CH CH599571A patent/CH557637A/xx not_active IP Right Cessation
-
1975
- 1975-07-08 KE KE2535*UA patent/KE2535A/xx unknown
- 1975-12-30 MY MY132/75A patent/MY7500132A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IE35120B1 (en) | 1975-11-12 |
| DE2020729C2 (de) | 1983-04-21 |
| BE766206A (fr) | 1971-10-25 |
| SE376150B (nl) | 1975-05-12 |
| FI52421B (nl) | 1977-05-31 |
| FR2086280B1 (nl) | 1974-10-11 |
| DK127363B (da) | 1973-10-29 |
| CY805A (en) | 1976-12-01 |
| PH9730A (en) | 1976-02-27 |
| IL36647A (en) | 1974-01-14 |
| EG10081A (en) | 1976-03-31 |
| FI52421C (fi) | 1977-09-12 |
| LU62709A1 (nl) | 1971-08-20 |
| DE2020729A1 (de) | 1972-01-05 |
| OA03621A (fr) | 1971-03-30 |
| ZA711634B (en) | 1971-11-24 |
| IL36647A0 (en) | 1971-06-23 |
| MY7500132A (en) | 1975-12-31 |
| RO58295A (nl) | 1975-08-15 |
| NL170088B (nl) | 1982-05-03 |
| GB1350264A (en) | 1974-04-18 |
| FR2086280A1 (nl) | 1971-12-31 |
| IE35120L (en) | 1971-10-23 |
| CH557637A (de) | 1975-01-15 |
| BG17708A3 (bg) | 1973-12-25 |
| JPS56402B1 (nl) | 1981-01-08 |
| AT309881B (de) | 1973-09-10 |
| BR7101940D0 (pt) | 1973-06-26 |
| CS167914B2 (nl) | 1976-05-28 |
| PL88965B3 (nl) | 1976-10-30 |
| CA962081A (en) | 1975-02-04 |
| KE2535A (en) | 1975-07-18 |
| TR20883A (tr) | 1982-11-22 |
| NL170088C (nl) | 1982-10-01 |
| HU162895B (nl) | 1973-04-28 |
| NL7105589A (nl) | 1971-10-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA014313B1 (ru) | Гербицидные средства и способ борьбы с ростом нежелательных растений | |
| DE2944783A1 (de) | Diphenylaetherderivate und herbizide | |
| DE1567164C2 (de) | Herbizide Mittel auf Basis von N-Carbamoyloxyphenyl-Carbamaten | |
| AU596635B2 (en) | Fungicidal compositions | |
| NO126458B (nl) | ||
| DE1468220A1 (de) | Selektive herbicide Mittel | |
| DE3909146A1 (de) | Herbizide ((1,3,5-triazin-2-yl) aminosulfonyl)benzoesaeureester, verfahren zu ihrer herstellung und ihre verwendung | |
| US3904396A (en) | Herbicidal mixture of several carbamoyloxyphenylcarbamates | |
| EP1545212B1 (en) | Herbicidal composition | |
| US4131751A (en) | Diurethanes | |
| DE2844806A1 (de) | Carbanilsaeure- eckige klammer auf 3-(alkylcarbonylamino)-phenyl eckige klammer zu -ester, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes herbizides mittel | |
| US4283547A (en) | Parabanic acid derivatives | |
| DE2310649C3 (de) | Diurethane sowie diese enthaltende selektive herbizide Mittel | |
| US3869275A (en) | Herbicidal mixtures | |
| CA1207547A (en) | Synergistic herbicidal combination | |
| AT275961B (de) | Herbizide Mittel mit verstärkter Wirksamkeit | |
| HU185779B (en) | Herbicides containing carbamic acid phenyl esters | |
| US3148048A (en) | Synergistic herbicidal composition | |
| DE2739349C3 (de) | N-O-Alkyl-phenyD-N'-methyl-N·methoxyharnstoffe und diese enthaltende Herbizide | |
| CA1187711A (en) | Synergistic herbicidal compositions | |
| US4004913A (en) | Selective herbicidal compositions | |
| US3546346A (en) | Systemic plant and seed fungicide comprising 1,1,1 - trichloro - 2 - hydroxy-3-nitropropane | |
| NO122047B (nl) | ||
| DE3413755A1 (de) | Thiazolylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses | |
| DE2310648A1 (de) | Selektive herbizide mittel |