SE460249B - Blandning foer reglering av vaexters tillvaext innehaallande som aktiv substans 2-cyano-2-etyl-2-fenylaettiksyraamid och/eller 2-cyano-2-etyl-2-fenylaettiksyramorfolid, anvaendning daerav samt 2-cyano-2-etyl-2-fenylaettiksyramorfolid - Google Patents
Blandning foer reglering av vaexters tillvaext innehaallande som aktiv substans 2-cyano-2-etyl-2-fenylaettiksyraamid och/eller 2-cyano-2-etyl-2-fenylaettiksyramorfolid, anvaendning daerav samt 2-cyano-2-etyl-2-fenylaettiksyramorfolidInfo
- Publication number
- SE460249B SE460249B SE8101304A SE8101304A SE460249B SE 460249 B SE460249 B SE 460249B SE 8101304 A SE8101304 A SE 8101304A SE 8101304 A SE8101304 A SE 8101304A SE 460249 B SE460249 B SE 460249B
- Authority
- SE
- Sweden
- Prior art keywords
- mixture
- cyano
- growth
- acid
- weight
- Prior art date
Links
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- 239000002253 acid Substances 0.000 title description 5
- 239000013543 active substance Substances 0.000 title description 4
- 238000002156 mixing Methods 0.000 title description 2
- 230000026267 regulation of growth Effects 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 31
- 239000007788 liquid Substances 0.000 claims description 19
- 239000004480 active ingredient Substances 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000007921 spray Substances 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 9
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- 239000003085 diluting agent Substances 0.000 claims description 6
- 239000012141 concentrate Substances 0.000 claims description 5
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 230000008635 plant growth Effects 0.000 claims description 3
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- 239000007787 solid Substances 0.000 claims description 2
- 238000007865 diluting Methods 0.000 claims 2
- 238000000034 method Methods 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
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- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
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- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
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- 239000007864 aqueous solution Substances 0.000 description 3
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- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- -1 kaulin Substances 0.000 description 3
- PTXLMDGMBJFHGQ-UHFFFAOYSA-N 2-(morpholine-4-carbonyl)-2-phenylbutanenitrile Chemical compound C=1C=CC=CC=1C(C#N)(CC)C(=O)N1CCOCC1 PTXLMDGMBJFHGQ-UHFFFAOYSA-N 0.000 description 2
- XAYBZYXKFHHIHQ-UHFFFAOYSA-N 2-cyano-2-phenylbutanoyl chloride Chemical compound CCC(C#N)(C(Cl)=O)C1=CC=CC=C1 XAYBZYXKFHHIHQ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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- 108010046377 Whey Proteins Proteins 0.000 description 2
- 150000001266 acyl halides Chemical class 0.000 description 2
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- 150000002148 esters Chemical class 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 150000002431 hydrogen 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
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
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- 239000003208 petroleum Substances 0.000 description 2
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- QXNQBFTWZZTGHQ-UHFFFAOYSA-N 12beta-O-Acetyl-coleon Z Natural products CC1CC11C(=O)C(C(OC(C)=O)C(O)C2C3(CCC(=C)C2=C)C)=C3C(=O)C1OC(C)=O QXNQBFTWZZTGHQ-UHFFFAOYSA-N 0.000 description 1
- GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 1
- QKSRTQXCXWMMLG-UHFFFAOYSA-N 2-cyano-2-phenylbutanamide Chemical compound CCC(C#N)(C(N)=O)C1=CC=CC=C1 QKSRTQXCXWMMLG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000945 Amylopectin Polymers 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
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- 241000208818 Helianthus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
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- 125000003710 aryl alkyl group Chemical group 0.000 description 1
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
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- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000008050 dialkyl sulfates Chemical class 0.000 description 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- XMHIUKTWLZUKEX-UHFFFAOYSA-N hexacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O XMHIUKTWLZUKEX-UHFFFAOYSA-N 0.000 description 1
- 239000003864 humus Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 238000009413 insulation Methods 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
- 238000005259 measurement Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 210000004197 pelvis Anatomy 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- SUSQOBVLVYHIEX-UHFFFAOYSA-N phenylacetonitrile Chemical compound N#CCC1=CC=CC=C1 SUSQOBVLVYHIEX-UHFFFAOYSA-N 0.000 description 1
- MTZWHHIREPJPTG-UHFFFAOYSA-N phorone Chemical compound CC(C)=CC(=O)C=C(C)C MTZWHHIREPJPTG-UHFFFAOYSA-N 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 230000035935 pregnancy Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
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- 238000005550 wet granulation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU80464A HU185876B (en) | 1980-02-29 | 1980-02-29 | Composition for controlling growth of plants and process for producing the active agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE8101304L SE8101304L (sv) | 1981-08-30 |
| SE460249B true SE460249B (sv) | 1989-09-25 |
Family
ID=10949708
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8101304A SE460249B (sv) | 1980-02-29 | 1981-02-27 | Blandning foer reglering av vaexters tillvaext innehaallande som aktiv substans 2-cyano-2-etyl-2-fenylaettiksyraamid och/eller 2-cyano-2-etyl-2-fenylaettiksyramorfolid, anvaendning daerav samt 2-cyano-2-etyl-2-fenylaettiksyramorfolid |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US4740228A (OSRAM) |
| JP (1) | JPS56135407A (OSRAM) |
| AT (1) | AT371667B (OSRAM) |
| AU (1) | AU544732B2 (OSRAM) |
| BE (1) | BE887683A (OSRAM) |
| CA (1) | CA1174866A (OSRAM) |
| CH (1) | CH646945A5 (OSRAM) |
| CS (1) | CS222243B2 (OSRAM) |
| DE (1) | DE3107629C2 (OSRAM) |
| DK (1) | DK92181A (OSRAM) |
| ES (1) | ES499940A0 (OSRAM) |
| FI (1) | FI65358C (OSRAM) |
| FR (2) | FR2483176A1 (OSRAM) |
| GB (1) | GB2072645B (OSRAM) |
| GR (1) | GR74096B (OSRAM) |
| HU (1) | HU185876B (OSRAM) |
| IL (1) | IL62228A (OSRAM) |
| IT (1) | IT1210996B (OSRAM) |
| NL (1) | NL8100962A (OSRAM) |
| PL (1) | PL128639B1 (OSRAM) |
| SE (1) | SE460249B (OSRAM) |
| SU (3) | SU1478991A3 (OSRAM) |
| YU (1) | YU41971B (OSRAM) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3265935A (en) * | 1963-08-30 | 1966-08-09 | Aerojet General Co | Modular chassis |
| US3751127A (en) * | 1970-09-10 | 1973-08-07 | Telecommunication Technology I | Modular instrument housing |
| SE7311226L (OSRAM) * | 1973-08-17 | 1975-02-18 | Expo Nord Ab | |
| US4162113A (en) * | 1977-05-09 | 1979-07-24 | Piero Pallavicini | Composite modular furniture |
| JPH01270020A (ja) * | 1988-04-22 | 1989-10-27 | Ryuichi Hayashi | 永久磁石を用いた光スイッチ |
| US5130456A (en) * | 1989-10-06 | 1992-07-14 | Virginia Tech Intellectual Properties, Inc. | Bis(reissert compounds) from reaction of monoaldehyde, monoamine and diacid halide |
| US5041601A (en) * | 1989-10-06 | 1991-08-20 | Virginia Tech Intellectual Properties, Inc. | Preparation of acyclic bis (reissert compounds) |
| EP0466640B1 (de) * | 1990-06-28 | 1995-05-24 | Ciba-Geigy Ag | Alpha-Carbonylphenylacetonitrilderivate als Stabilisatoren für organische Materialien |
| ATE239371T1 (de) | 1999-03-02 | 2003-05-15 | Basf Ag | Verwendung von phenylessigsaüreamide als pflanzenschutzmittel mit herbizider und fungizider wirkung |
| US6462076B2 (en) * | 2000-06-14 | 2002-10-08 | Hoffmann-La Roche Inc. | Beta-amino acid nitrile derivatives as cathepsin K inhibitors |
| JP4928276B2 (ja) * | 2007-01-11 | 2012-05-09 | オタリ株式会社 | フィルム除去装置 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2412510A (en) * | 1944-06-02 | 1946-12-10 | American Chem Paint Co | Methods and compositions for killing weeds |
| US3020146A (en) * | 1958-09-22 | 1962-02-06 | Velsicol Chemical Corp | Method of destroying undesirable plants |
| DE1542777C3 (de) * | 1965-04-17 | 1978-12-07 | Bayer Ag, 5090 Leverkusen | a-ChIor-ß-(4-chlorphenyl) propionsäruemethylester und Herbizide mit einem Gehalt an einem cx-Chlorß-phenylpropionsäruederivat |
| DE1542822A1 (de) * | 1966-03-10 | 1970-03-26 | Basf Ag | Selektive Herbizide |
| JPS5353617A (en) * | 1976-10-23 | 1978-05-16 | Tanabe Seiyaku Co Ltd | Alpha-isocyano fatty acid amide derivatives and process for preparation of thesame |
| DE2751782A1 (de) * | 1977-11-19 | 1979-05-23 | Bayer Ag | Mittel zur regulierung des pflanzenwachstums |
| US4313754A (en) * | 1978-05-05 | 1982-02-02 | American Cyanamid Company | Polysubstituted butanoic acids, esters and derivatives thereof utilizing the same as herbicides |
| DE2842639A1 (de) * | 1978-09-29 | 1980-04-10 | Bayer Ag | Alpha -isocyano-carbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als pflanzenwachstumsregulatoren |
-
1980
- 1980-02-29 HU HU80464A patent/HU185876B/hu not_active IP Right Cessation
-
1981
- 1981-02-26 BE BE1/10151A patent/BE887683A/fr not_active IP Right Cessation
- 1981-02-26 CH CH129281A patent/CH646945A5/de not_active IP Right Cessation
- 1981-02-27 IT IT8120025A patent/IT1210996B/it active
- 1981-02-27 CS CS811442A patent/CS222243B2/cs unknown
- 1981-02-27 PL PL1981229912A patent/PL128639B1/pl unknown
- 1981-02-27 CA CA000371912A patent/CA1174866A/en not_active Expired
- 1981-02-27 SE SE8101304A patent/SE460249B/sv not_active IP Right Cessation
- 1981-02-27 SU SU813325354A patent/SU1478991A3/ru active
- 1981-02-27 FI FI810629A patent/FI65358C/fi not_active IP Right Cessation
- 1981-02-27 FR FR8103917A patent/FR2483176A1/fr active Granted
- 1981-02-27 GR GR64254A patent/GR74096B/el unknown
- 1981-02-27 DK DK92181A patent/DK92181A/da not_active Application Discontinuation
- 1981-02-27 AT AT0091581A patent/AT371667B/de not_active IP Right Cessation
- 1981-02-27 DE DE3107629A patent/DE3107629C2/de not_active Expired
- 1981-02-27 GB GB8106327A patent/GB2072645B/en not_active Expired
- 1981-02-27 YU YU500/81A patent/YU41971B/xx unknown
- 1981-02-27 AU AU67920/81A patent/AU544732B2/en not_active Ceased
- 1981-02-27 NL NL8100962A patent/NL8100962A/nl not_active Application Discontinuation
- 1981-02-27 IL IL62228A patent/IL62228A/xx unknown
- 1981-02-28 JP JP2929881A patent/JPS56135407A/ja active Granted
- 1981-02-28 ES ES499940A patent/ES499940A0/es active Granted
- 1981-11-17 FR FR8121446A patent/FR2491061A1/fr active Granted
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1982
- 1982-09-20 SU SU823493198A patent/SU1318152A3/ru active
- 1982-09-20 SU SU823491803A patent/SU1389677A3/ru active
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1984
- 1984-01-10 US US06/569,594 patent/US4740228A/en not_active Expired - Fee Related
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