DD145991A5 - Landwirtschaftlich verwendbare zusammensetzung - Google Patents
Landwirtschaftlich verwendbare zusammensetzung Download PDFInfo
- Publication number
- DD145991A5 DD145991A5 DD79215206A DD21520679A DD145991A5 DD 145991 A5 DD145991 A5 DD 145991A5 DD 79215206 A DD79215206 A DD 79215206A DD 21520679 A DD21520679 A DD 21520679A DD 145991 A5 DD145991 A5 DD 145991A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- growth
- plant
- plants
- active ingredient
- leaf
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- 239000000654 additive Substances 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 5
- 150000002367 halogens Chemical group 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
- 150000002431 hydrogen Chemical group 0.000 claims abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 2
- 230000012010 growth Effects 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- 239000000969 carrier Substances 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 abstract description 20
- 230000002363 herbicidal effect Effects 0.000 abstract description 16
- 239000004009 herbicide Substances 0.000 abstract description 9
- 239000005648 plant growth regulator Substances 0.000 abstract description 8
- 241000196324 Embryophyta Species 0.000 description 39
- 230000005764 inhibitory process Effects 0.000 description 18
- 230000008859 change Effects 0.000 description 12
- 230000008635 plant growth Effects 0.000 description 12
- 150000003949 imides Chemical class 0.000 description 11
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 230000002015 leaf growth Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 150000001408 amides Chemical class 0.000 description 7
- -1 butyric acid imide Chemical class 0.000 description 7
- 230000001105 regulatory effect Effects 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 230000004075 alteration Effects 0.000 description 6
- 150000008064 anhydrides Chemical class 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000001953 recrystallisation Methods 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical class CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000018109 developmental process Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- SNQBHCMKAXUWBD-UHFFFAOYSA-N 2-(6-bromo-2-oxo-1,3-benzothiazol-3-yl)acetamide Chemical compound C1=C(Br)C=C2SC(=O)N(CC(=O)N)C2=C1 SNQBHCMKAXUWBD-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-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
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- 239000001632 sodium acetate Substances 0.000 description 3
- 235000017281 sodium acetate Nutrition 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 235000021374 legumes Nutrition 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000009331 sowing Methods 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- SXOCCTHWTPGZHT-UHFFFAOYSA-N 2-(2-oxo-1,3-benzothiazol-3-yl)acetic acid Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1 SXOCCTHWTPGZHT-UHFFFAOYSA-N 0.000 description 1
- DYURLFRNFJUQCA-UHFFFAOYSA-N 2-(5-chloro-2-oxo-1,3-benzothiazol-3-yl)acetamide Chemical compound ClC1=CC=C2SC(=O)N(CC(=O)N)C2=C1 DYURLFRNFJUQCA-UHFFFAOYSA-N 0.000 description 1
- IKVOFYRQWZWUQF-UHFFFAOYSA-N 2-(6-nitro-2-oxo-1,3-benzothiazol-3-yl)acetamide Chemical compound C1=C([N+]([O-])=O)C=C2SC(=O)N(CC(=O)N)C2=C1 IKVOFYRQWZWUQF-UHFFFAOYSA-N 0.000 description 1
- TYEYBOSBBBHJIV-UHFFFAOYSA-N 2-oxobutanoic acid Chemical class CCC(=O)C(O)=O TYEYBOSBBBHJIV-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 240000006995 Abutilon theophrasti Species 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 235000021533 Beta vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241001148727 Bromus tectorum Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 240000001579 Cirsium arvense Species 0.000 description 1
- 235000005918 Cirsium arvense Nutrition 0.000 description 1
- 244000285774 Cyperus esculentus Species 0.000 description 1
- 235000005853 Cyperus esculentus Nutrition 0.000 description 1
- 244000152970 Digitaria sanguinalis Species 0.000 description 1
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
- 241000508725 Elymus repens Species 0.000 description 1
- 241001289540 Fallopia convolvulus Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 235000021506 Ipomoea Nutrition 0.000 description 1
- 241000207783 Ipomoea Species 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 241000209117 Panicum Species 0.000 description 1
- 244000088461 Panicum crus-galli Species 0.000 description 1
- 235000011999 Panicum crusgalli Nutrition 0.000 description 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
- 241000978467 Persicaria pensylvanica Species 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 241000533293 Sesbania emerus Species 0.000 description 1
- 241000209072 Sorghum Species 0.000 description 1
- 240000002439 Sorghum halepense Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 244000067505 Xanthium strumarium Species 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 235000010633 broth Nutrition 0.000 description 1
- YHASWHZGWUONAO-UHFFFAOYSA-N butanoyl butanoate Chemical compound CCCC(=O)OC(=O)CCC YHASWHZGWUONAO-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000036253 epinasty Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000002786 root growth Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- MFBOGIVSZKQAPD-UHFFFAOYSA-M sodium butyrate Chemical compound [Na+].CCCC([O-])=O MFBOGIVSZKQAPD-UHFFFAOYSA-M 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/937,231 US4185990A (en) | 1978-08-28 | 1978-08-28 | Imides derived from 2-oxo-3-benzothiazolineacetic acid and butyric acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD145991A5 true DD145991A5 (de) | 1981-01-21 |
Family
ID=25469653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79215206A DD145991A5 (de) | 1978-08-28 | 1979-08-27 | Landwirtschaftlich verwendbare zusammensetzung |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4185990A (cs) |
| EP (1) | EP0009331B1 (cs) |
| JP (1) | JPS5533491A (cs) |
| AR (1) | AR222188A1 (cs) |
| AT (1) | ATE4208T1 (cs) |
| AU (1) | AU522067B2 (cs) |
| BG (1) | BG30620A3 (cs) |
| BR (1) | BR7905479A (cs) |
| CA (1) | CA1125766A (cs) |
| CS (1) | CS208675B2 (cs) |
| DD (1) | DD145991A5 (cs) |
| DE (1) | DE2965922D1 (cs) |
| DK (1) | DK357379A (cs) |
| ES (1) | ES483627A1 (cs) |
| GR (1) | GR68054B (cs) |
| HU (1) | HU186350B (cs) |
| IL (1) | IL58117A (cs) |
| MX (1) | MX6438E (cs) |
| PL (1) | PL119269B1 (cs) |
| RO (1) | RO78880A (cs) |
| TR (1) | TR20491A (cs) |
| ZA (1) | ZA794502B (cs) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4422865A (en) * | 1981-01-09 | 1983-12-27 | Monsanto Company | Imides derived from 2-thioxo-3-(benzox (thia) azoline acetic and propionic acids |
| MX2013007379A (es) | 2010-12-21 | 2013-07-15 | Bayer Cropscience Lp | Mutantes tipo papel lija de bacillus y metodos de uso de los mismos para mejorar el crecimiento vegetal, promover la salud de plantas y controlar enfermedades y plagas. |
| WO2013039937A1 (en) | 2011-09-12 | 2013-03-21 | Agraquest, Inc. | Methods of enhancing health and/or promoting growth of a plant and/or of improving fruit ripening |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL108409C (cs) * | 1958-10-29 | |||
| US4049419A (en) * | 1975-05-12 | 1977-09-20 | Monsanto Company | Use of benzothiazoline compounds as plant growth regulants |
| US3993468A (en) * | 1975-05-12 | 1976-11-23 | Monsanto Company | Use of 3-substituted benzothiazolines as plant growth regulants |
| US4086241A (en) * | 1976-06-14 | 1978-04-25 | Velsicol Chemical Corporation | Benzothiazolylimidazolidinone esters of furyl and thienyl substituted acids |
| US4075216A (en) * | 1976-10-26 | 1978-02-21 | Monsanto Company | Certain benzothiazolin-2-one derivatives |
-
1978
- 1978-08-28 US US05/937,231 patent/US4185990A/en not_active Expired - Lifetime
-
1979
- 1979-08-24 ES ES483627A patent/ES483627A1/es not_active Expired
- 1979-08-24 DE DE7979301739T patent/DE2965922D1/de not_active Expired
- 1979-08-24 EP EP79301739A patent/EP0009331B1/en not_active Expired
- 1979-08-24 AT AT79301739T patent/ATE4208T1/de not_active IP Right Cessation
- 1979-08-27 DK DK357379A patent/DK357379A/da not_active Application Discontinuation
- 1979-08-27 PL PL1979217977A patent/PL119269B1/pl unknown
- 1979-08-27 AR AR277861A patent/AR222188A1/es active
- 1979-08-27 BG BG044755A patent/BG30620A3/xx unknown
- 1979-08-27 MX MX798345U patent/MX6438E/es unknown
- 1979-08-27 JP JP10824779A patent/JPS5533491A/ja active Pending
- 1979-08-27 CA CA334,513A patent/CA1125766A/en not_active Expired
- 1979-08-27 AU AU50324/79A patent/AU522067B2/en not_active Ceased
- 1979-08-27 HU HU79MO1061A patent/HU186350B/hu unknown
- 1979-08-27 GR GR59912A patent/GR68054B/el unknown
- 1979-08-27 CS CS795814A patent/CS208675B2/cs unknown
- 1979-08-27 BR BR7905479A patent/BR7905479A/pt unknown
- 1979-08-27 ZA ZA00794502A patent/ZA794502B/xx unknown
- 1979-08-27 RO RO7998526A patent/RO78880A/ro unknown
- 1979-08-27 DD DD79215206A patent/DD145991A5/de unknown
- 1979-08-27 TR TR20491A patent/TR20491A/xx unknown
- 1979-08-27 IL IL58117A patent/IL58117A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE4208T1 (de) | 1983-08-15 |
| CS208675B2 (en) | 1981-09-15 |
| IL58117A0 (en) | 1979-12-30 |
| BR7905479A (pt) | 1980-05-20 |
| DE2965922D1 (en) | 1983-08-25 |
| DK357379A (da) | 1980-02-29 |
| TR20491A (tr) | 1981-08-14 |
| EP0009331A1 (en) | 1980-04-02 |
| MX6438E (es) | 1985-05-31 |
| BG30620A3 (en) | 1981-07-15 |
| HU186350B (en) | 1985-07-29 |
| IL58117A (en) | 1982-07-30 |
| EP0009331B1 (en) | 1983-07-20 |
| PL119269B1 (en) | 1981-12-31 |
| US4185990A (en) | 1980-01-29 |
| JPS5533491A (en) | 1980-03-08 |
| PL217977A1 (cs) | 1980-08-11 |
| RO78880A (ro) | 1982-08-17 |
| ZA794502B (en) | 1980-08-27 |
| AR222188A1 (es) | 1981-04-30 |
| ES483627A1 (es) | 1980-09-01 |
| AU522067B2 (en) | 1982-05-13 |
| CA1125766A (en) | 1982-06-15 |
| AU5032479A (en) | 1980-03-06 |
| GR68054B (cs) | 1981-10-29 |
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