DD145992A5 - Pflanzenwachstumsregulator - Google Patents
Pflanzenwachstumsregulator Download PDFInfo
- Publication number
- DD145992A5 DD145992A5 DD78209810A DD20981078A DD145992A5 DD 145992 A5 DD145992 A5 DD 145992A5 DD 78209810 A DD78209810 A DD 78209810A DD 20981078 A DD20981078 A DD 20981078A DD 145992 A5 DD145992 A5 DD 145992A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- plant growth
- growth regulator
- change
- plants
- plant
- Prior art date
Links
- 239000005648 plant growth regulator Substances 0.000 title claims description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 11
- 230000008635 plant growth Effects 0.000 claims abstract description 10
- -1 2-benzthiazolyl Chemical group 0.000 claims abstract description 9
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000001257 hydrogen Substances 0.000 claims abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 2
- 239000000654 additive Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 4
- 239000000969 carrier Substances 0.000 claims description 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 abstract description 13
- 230000001105 regulatory effect Effects 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 abstract description 6
- 101100072620 Streptomyces griseus ind2 gene Proteins 0.000 abstract 2
- 241000196324 Embryophyta Species 0.000 description 28
- 230000008859 change Effects 0.000 description 21
- 235000021374 legumes Nutrition 0.000 description 11
- 230000009467 reduction Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 230000005764 inhibitory process Effects 0.000 description 8
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 244000068988 Glycine max Species 0.000 description 5
- 230000012010 growth Effects 0.000 description 5
- 230000011890 leaf development Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000018109 developmental process Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-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
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 238000003306 harvesting Methods 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- MRHAAMBNOQKMMW-UHFFFAOYSA-N 2-(2-oxo-1,3-benzothiazol-3-yl)acetamide Chemical class C1=CC=C2SC(=O)N(CC(=O)N)C2=C1 MRHAAMBNOQKMMW-UHFFFAOYSA-N 0.000 description 2
- BSQLQMLFTHJVKS-UHFFFAOYSA-N 2-chloro-1,3-benzothiazole Chemical compound C1=CC=C2SC(Cl)=NC2=C1 BSQLQMLFTHJVKS-UHFFFAOYSA-N 0.000 description 2
- GBHCABUWWQUMAJ-UHFFFAOYSA-N 2-hydrazinoethanol Chemical compound NNCCO GBHCABUWWQUMAJ-UHFFFAOYSA-N 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000004075 alteration Effects 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 230000036253 epinasty Effects 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000029553 photosynthesis Effects 0.000 description 2
- 238000010672 photosynthesis Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- BXQNSPXDWSNUKE-UHFFFAOYSA-N 1,3-benzothiazole 1-oxide Chemical compound C1=CC=C2S(=O)C=NC2=C1 BXQNSPXDWSNUKE-UHFFFAOYSA-N 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 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
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000002679 ablation Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N alpha-methyl toluene Natural products CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- UGBKOURNNQREPE-UHFFFAOYSA-N azepan-1-amine Chemical compound NN1CCCCCC1 UGBKOURNNQREPE-UHFFFAOYSA-N 0.000 description 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- LWMPFIOTEAXAGV-UHFFFAOYSA-N piperidin-1-amine Chemical compound NN1CCCCC1 LWMPFIOTEAXAGV-UHFFFAOYSA-N 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
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000021251 pulses Nutrition 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000026267 regulation of growth Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003826 tablet Substances 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
- 230000005068 transpiration Effects 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000013585 weight reducing agent 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
-
- 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
- C07D277/82—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Cultivation Of Plants (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/861,479 US4187097A (en) | 1977-12-16 | 1977-12-16 | N-hydrazides of 2-benzothiazolinone as plant growth regulants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD145992A5 true DD145992A5 (de) | 1981-01-21 |
Family
ID=25335922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD78209810A DD145992A5 (de) | 1977-12-16 | 1978-12-15 | Pflanzenwachstumsregulator |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US4187097A (cs) |
| EP (1) | EP0002613A1 (cs) |
| JP (1) | JPS5924978B2 (cs) |
| AR (1) | AR222983A1 (cs) |
| AU (1) | AU517707B2 (cs) |
| BG (1) | BG31213A3 (cs) |
| BR (1) | BR7808242A (cs) |
| CA (1) | CA1107281A (cs) |
| CS (1) | CS204955B2 (cs) |
| DD (1) | DD145992A5 (cs) |
| DK (1) | DK565578A (cs) |
| HU (1) | HU182538B (cs) |
| IL (1) | IL56226A (cs) |
| IT (1) | IT1100640B (cs) |
| MX (1) | MX5412E (cs) |
| PL (1) | PL114598B1 (cs) |
| ZA (1) | ZA787027B (cs) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4228292A (en) * | 1978-07-20 | 1980-10-14 | Monsanto Company | N-Substituted benzothiazolines and benzoxazolines and their use as herbicides and plant growth regulants |
| DE3835576A1 (de) * | 1988-03-25 | 1989-10-12 | Bayer Ag | 3,7-disubstituierte benzthiazolone |
| US6190432B1 (en) | 1999-02-26 | 2001-02-20 | Donaldson Company, Inc. | Filter arrangement; sealing system; and methods |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL108409C (cs) * | 1958-10-29 | |||
| US3249621A (en) * | 1964-10-16 | 1966-05-03 | Monsanto Co | 3-(2-benzothiazolyl)-2-benzothiazolinone |
| CA928296A (en) * | 1967-06-05 | 1973-06-12 | Umio Suminori | N-substituted and n, n-disubstituted aminocarbonylalkyl compounds and their production |
| DE2101150A1 (de) * | 1971-01-12 | 1972-08-03 | Farbenfabriken Bayer Ag, 5090 Leverkusen | Substituierte Benzthiazolone, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Akarizide und Insektizide |
| AT334133B (de) * | 1974-12-17 | 1976-12-27 | Chemie Linz Ag | Herbizides mittel |
| 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 |
| US4057415A (en) * | 1976-06-18 | 1977-11-08 | Fmc Corporation | Nitroisothiazolylureas as herbicides |
| US4075216A (en) * | 1976-10-26 | 1978-02-21 | Monsanto Company | Certain benzothiazolin-2-one derivatives |
-
1977
- 1977-12-16 US US05/861,479 patent/US4187097A/en not_active Expired - Lifetime
-
1978
- 1978-12-14 EP EP78300818A patent/EP0002613A1/en not_active Withdrawn
- 1978-12-15 DK DK565578A patent/DK565578A/da not_active Application Discontinuation
- 1978-12-15 JP JP53154313A patent/JPS5924978B2/ja not_active Expired
- 1978-12-15 AR AR274821A patent/AR222983A1/es active
- 1978-12-15 BG BG041751A patent/BG31213A3/xx unknown
- 1978-12-15 IT IT30916/78A patent/IT1100640B/it active
- 1978-12-15 CA CA318,063A patent/CA1107281A/en not_active Expired
- 1978-12-15 CS CS788404A patent/CS204955B2/cs unknown
- 1978-12-15 IL IL56226A patent/IL56226A/xx unknown
- 1978-12-15 BR BR7808242A patent/BR7808242A/pt unknown
- 1978-12-15 PL PL1978211796A patent/PL114598B1/pl unknown
- 1978-12-15 MX MX787603U patent/MX5412E/es unknown
- 1978-12-15 AU AU42583/78A patent/AU517707B2/en not_active Expired
- 1978-12-15 DD DD78209810A patent/DD145992A5/de unknown
- 1978-12-15 ZA ZA00787027A patent/ZA787027B/xx unknown
- 1978-12-29 HU HU78MO1029A patent/HU182538B/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IT1100640B (it) | 1985-09-28 |
| CS204955B2 (en) | 1981-04-30 |
| IL56226A0 (en) | 1979-03-12 |
| AU4258378A (en) | 1979-06-21 |
| JPS5924978B2 (ja) | 1984-06-13 |
| CA1107281A (en) | 1981-08-18 |
| JPS5488265A (en) | 1979-07-13 |
| PL114598B1 (en) | 1981-02-28 |
| AU517707B2 (en) | 1981-08-20 |
| BG31213A3 (en) | 1981-11-16 |
| US4187097A (en) | 1980-02-05 |
| DK565578A (da) | 1979-06-17 |
| IT7830916A0 (it) | 1978-12-15 |
| EP0002613A1 (en) | 1979-06-27 |
| IL56226A (en) | 1981-09-13 |
| HU182538B (en) | 1984-02-28 |
| MX5412E (es) | 1983-07-20 |
| ZA787027B (en) | 1979-11-28 |
| PL211796A1 (pl) | 1979-08-27 |
| BR7808242A (pt) | 1979-08-14 |
| AR222983A1 (es) | 1981-07-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2843722C2 (de) | N-(2-Chlor-4-pyridyl)-N'-phenyl-harnstoffe, Verfahren zu deren Herstellung sowie diese enthaltende Pflanzenwachstumsregulatoren | |
| EP0010770B1 (de) | In 2-Stellung substituierte 4-Pyridyl-harnstoffe bzw. -thioharnstoffe, Verfahren zu deren Herstellung sowie diese enthaltende Pflanzenwachstumsregulatoren | |
| DE3415820A1 (de) | 1-carbalkoxyalkyl-3-aryloxy-4-(2'-carboxyphenyl)-azet-2-one, diese enthaltende pflanzenwachstumsregulierende mittel und verfahren zum regulieren des pflanzenwachstums | |
| EP0005782B1 (de) | Pflanzenwachstum regulierende Verbindungen, deren Verwendung und Herstellung sowie diese Verbindungen enthaltende Mittel, deren Verwendung und Herstellung | |
| EP0025141A1 (de) | Verfahren zur Herstellung von 1-Amino-cyclopropan-carbonsäure und deren Derivaten | |
| EP0010143A2 (de) | Oxim-Derivate zum Schutz von Pflanzenkulturen | |
| DD145881A5 (de) | Zusammensetzung zum regulieren des pflanzenwuchses | |
| DE2657380C3 (de) | Halogenäthyl-sulfone, Verfahren zu ihrer Herstellung sowie ihre Verwendung zur Regulierung des Pflanzenwachstums | |
| DE3133917A1 (de) | 1-amino-cyclopropancarbonsaeure-metallkomplexverbindungen, verfahren zu deren herstellung und deren verwendung als pflanzenwachstumsregulatoren | |
| DE2416004A1 (de) | Regulatoren fuer das pflanzenwachstum | |
| EP0002014B1 (de) | Alpha-isocyanocarbonsäure-Salze, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenwachstumsregulatoren | |
| DD145992A5 (de) | Pflanzenwachstumsregulator | |
| DE3144526C2 (cs) | ||
| DD144502A5 (de) | Pflanzenwachstumsregulator | |
| EP0002455B1 (de) | Acyloxyamide, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Pflanzenwachstumsregulatoren | |
| DD257255A5 (de) | Verfahren zur herstellung von neuen mono- oder di-(aryloxyethyl)succinaten | |
| EP0009710B1 (de) | Alpha-Isocyano-cyclopropan-carbonsäureamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenwachstumsregulatoren | |
| DE2362333C3 (de) | Thionophosphorsäureesteramide, Verfahren zu deren Herstellung und Verwendung derselben | |
| EP0002013A1 (de) | Mittel zur Regulierung des Pflanzenwachstums, deren Herstellung sowie die Verwendung von alpha-Isocyanocarbonsäurederivaten zur Regulierung des Pflanzenwachstums | |
| DD241821A3 (de) | Mittel zur beeinflussung von wachstums-,entwicklungs- und stoffwechselprozessen in pflanzen | |
| DE2149680C3 (de) | 2-Halogenäthyl-organooxy-sllane, deren Herstelung und Mittel zur Regulierung des Pflanzenwachstums CIBA-GEIGY AG, Basel (Schweiz) | |
| DE4011781A1 (de) | Herbizides mittel | |
| DD140839A5 (de) | Pflanzenwachstumsregulator auf der basis von n-substituierten oxobenzthiazolinen | |
| DD145991A5 (de) | Landwirtschaftlich verwendbare zusammensetzung | |
| AT280320B (de) | Pflanzenwuchsmittel |