DD152902A5 - Pflanzenwachstumsregulator - Google Patents

Pflanzenwachstumsregulator Download PDF

Info

Publication number: DD152902A5
Authority: DD; German Democratic Republic
Prior art keywords: plant; plant growth; plants; growth regulator; leaf
Prior art date: 1979-08-23

Application number

DD80223460A

Other languages

German (de)

English (en)

Inventor

Amico John J D

John T Marvel

Original Assignee

Amico John J D

John T Marvel

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1979-08-23

Filing date

1980-08-22

Publication date

1981-12-16

1980-08-22 Application filed by Amico John J D, John T Marvel filed Critical Amico John J D

1981-12-16 Publication of DD152902A5 publication Critical patent/DD152902A5/de

Links

239000005648 plant growth regulator Substances 0.000 title claims description 12
150000001875 compounds Chemical class 0.000 claims abstract description 14
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 7
229910052736 halogen Inorganic materials 0.000 claims abstract description 7
229910052717 sulfur Inorganic materials 0.000 claims abstract description 6
239000011593 sulfur Substances 0.000 claims abstract description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 5
229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
239000001301 oxygen Substances 0.000 claims abstract description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 3
150000002367 halogens Chemical group 0.000 claims description 5
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
239000004480 active ingredient Substances 0.000 abstract description 11
230000012010 growth Effects 0.000 abstract description 11
239000000203 mixture Substances 0.000 abstract description 10
230000001105 regulatory effect Effects 0.000 abstract description 5
239000000126 substance Substances 0.000 abstract description 3
125000005843 halogen group Chemical group 0.000 abstract 2
239000004606 Fillers/Extenders Substances 0.000 abstract 1
239000000546 pharmaceutical excipient Substances 0.000 abstract 1
239000000700 radioactive tracer Substances 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 40
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 13
230000005764 inhibitory process Effects 0.000 description 11
230000004048 modification Effects 0.000 description 9
238000012986 modification Methods 0.000 description 9
230000008859 change Effects 0.000 description 8
235000021374 legumes Nutrition 0.000 description 8
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
230000008635 plant growth Effects 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
244000068988 Glycine max Species 0.000 description 6
238000011161 development Methods 0.000 description 6
230000018109 developmental process Effects 0.000 description 6
230000000694 effects Effects 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
-1 For example Chemical class 0.000 description 4
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
230000033228 biological regulation Effects 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000000463 material Substances 0.000 description 4
238000000034 method Methods 0.000 description 4
239000002689 soil Substances 0.000 description 4
235000010469 Glycine max Nutrition 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
238000001953 recrystallisation Methods 0.000 description 3
239000007921 spray Substances 0.000 description 3
239000000758 substrate Substances 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
150000007960 acetonitrile Chemical class 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
230000004075 alteration Effects 0.000 description 2
239000002585 base Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003795 chemical substances by application Substances 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
238000004519 manufacturing process Methods 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000002243 precursor Substances 0.000 description 2
230000009467 reduction Effects 0.000 description 2
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
NNLNFBHGCUPRGY-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)ethanimidamide Chemical class C1=CC=C2SC(CC(=N)N)=NC2=C1 NNLNFBHGCUPRGY-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
208000035859 Drug effect increased Diseases 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 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
230000001133 acceleration Effects 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
230000009471 action Effects 0.000 description 1
239000013543 active substance Substances 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
150000008044 alkali metal hydroxides 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
239000000908 ammonium hydroxide Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
150000001720 carbohydrates Chemical class 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
230000003750 conditioning 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
230000003247 decreasing effect Effects 0.000 description 1
230000008021 deposition Effects 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
230000005094 fruit set Effects 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
208000006278 hypochromic anemia Diseases 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
230000001795 light effect Effects 0.000 description 1
239000003595 mist Substances 0.000 description 1
230000000877 morphologic effect Effects 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000008188 pellet Substances 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000029553 photosynthesis Effects 0.000 description 1
238000010672 photosynthesis Methods 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
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
229910000027 potassium carbonate Inorganic materials 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
230000005068 transpiration Effects 0.000 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
238000011179 visual inspection Methods 0.000 description 1
235000020234 walnut Nutrition 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
- C07D277/70—Sulfur atoms

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)
Cultivation Of Plants (AREA)
Thiazole And Isothizaole Compounds (AREA)

DD80223460A 1979-08-23 1980-08-22 Pflanzenwachstumsregulator DD152902A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/068,993 US4283220A (en)	1979-08-23	1979-08-23	Imidamides derived from 2-oxo-3-benzothiazoline acetic acid plant growth regulants

Publications (1)

Publication Number	Publication Date
DD152902A5 true DD152902A5 (de)	1981-12-16

Family

ID=22086018

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD80223460A DD152902A5 (de)	1979-08-23	1980-08-22	Pflanzenwachstumsregulator

Country Status (20)

Country	Link
US (1)	US4283220A (fi)
EP (1)	EP0024889A1 (fi)
JP (1)	JPS5677270A (fi)
KR (1)	KR840001933B1 (fi)
AR (1)	AR224418A1 (fi)
AU (1)	AU530437B2 (fi)
BG (1)	BG31502A3 (fi)
BR (1)	BR8005341A (fi)
CA (1)	CA1148959A (fi)
CS (1)	CS214840B2 (fi)
DD (1)	DD152902A5 (fi)
DK (1)	DK361480A (fi)
FI (1)	FI802660A (fi)
IL (1)	IL60895A (fi)
IN (1)	IN153446B (fi)
NO (1)	NO802503L (fi)
NZ (1)	NZ194736A (fi)
PL (1)	PL226365A1 (fi)
YU (1)	YU202580A (fi)
ZA (1)	ZA805182B (fi)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH04217579A (ja) *	1990-12-13	1992-08-07	Mitsubishi Electric Corp	エレベータロープの横揺れ防止装置

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1792770A (en) *	1924-11-18	1931-02-17	Goodyear Tire & Rubber	Vulcanization of rubber and method of producing same
US2947782A (en) *	1957-12-23	1960-08-02	Rohm & Haas	Aminoacetamidoximes
NL108409C (fi) *	1958-10-29
US3717690A (en) *	1970-07-01	1973-02-20	Exxon Research Engineering Co	N,n-dialkylamidoxime phosphates
US3923491A (en) *	1973-08-09	1975-12-02	Allied Chem	Growth regulants for plants
JPS577122B2 (fi) *	1973-12-24	1982-02-09
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
US4075216A (en) *	1976-10-26	1978-02-21	Monsanto Company	Certain benzothiazolin-2-one derivatives

1979
- 1979-08-23 US US06/068,993 patent/US4283220A/en not_active Expired - Lifetime
1980
- 1980-08-12 YU YU02025/80A patent/YU202580A/xx unknown
- 1980-08-21 KR KR1019800003304A patent/KR840001933B1/ko active
- 1980-08-21 AR AR282243A patent/AR224418A1/es active
- 1980-08-21 EP EP80302897A patent/EP0024889A1/en not_active Withdrawn
- 1980-08-22 ZA ZA00805182A patent/ZA805182B/xx unknown
- 1980-08-22 BG BG048910A patent/BG31502A3/xx unknown
- 1980-08-22 CS CS805769A patent/CS214840B2/cs unknown
- 1980-08-22 CA CA000358958A patent/CA1148959A/en not_active Expired
- 1980-08-22 NZ NZ194736A patent/NZ194736A/xx unknown
- 1980-08-22 DD DD80223460A patent/DD152902A5/de unknown
- 1980-08-22 IL IL60895A patent/IL60895A/xx unknown
- 1980-08-22 PL PL22636580A patent/PL226365A1/xx unknown
- 1980-08-22 AU AU61679/80A patent/AU530437B2/en not_active Ceased
- 1980-08-22 BR BR8005341A patent/BR8005341A/pt unknown
- 1980-08-22 IN IN963/CAL/80A patent/IN153446B/en unknown
- 1980-08-22 FI FI802660A patent/FI802660A/fi not_active Application Discontinuation
- 1980-08-22 DK DK361480A patent/DK361480A/da not_active Application Discontinuation
- 1980-08-22 NO NO802503A patent/NO802503L/no unknown
- 1980-08-22 JP JP11488080A patent/JPS5677270A/ja active Pending

Also Published As

Publication number	Publication date
PL226365A1 (fi)	1981-06-05
NZ194736A (en)	1983-02-15
FI802660A (fi)	1981-02-24
IN153446B (fi)	1984-07-14
IL60895A (en)	1983-11-30
BG31502A3 (en)	1982-01-15
YU202580A (en)	1983-04-30
DK361480A (da)	1981-02-24
CS214840B2 (en)	1982-06-25
BR8005341A (pt)	1981-03-04
NO802503L (no)	1981-02-24
JPS5677270A (en)	1981-06-25
KR830003451A (ko)	1983-06-20
ZA805182B (en)	1981-09-30
AU6167980A (en)	1981-03-05
EP0024889A1 (en)	1981-03-11
CA1148959A (en)	1983-06-28
IL60895A0 (en)	1980-10-26
US4283220A (en)	1981-08-11
AR224418A1 (es)	1981-11-30
KR840001933B1 (ko)	1984-10-25
AU530437B2 (en)	1983-07-14

Publication	Publication Date	Title
DE2843722C2 (de)	1986-10-23	N-(2-Chlor-4-pyridyl)-N'-phenyl-harnstoffe, Verfahren zu deren Herstellung sowie diese enthaltende Pflanzenwachstumsregulatoren
EP0010770B1 (de)	1982-07-07	In 2-Stellung substituierte 4-Pyridyl-harnstoffe bzw. -thioharnstoffe, Verfahren zu deren Herstellung sowie diese enthaltende Pflanzenwachstumsregulatoren
DE2223894C3 (de)	1981-07-23	Herbizide Mittel auf Basis von Phenoxycarbonsäurederivaten
DE2350944C2 (de)	1982-12-23	N-(1'-Methoxycarbonyl-äthyl)-N-haloacetyl-2-6- dialkylaniline, Verfahren zu deren Herstellung und diese Verbindungen enthaltende fungizide Mittel
EP0036390B1 (de)	1983-10-26	Diphenyläther-Harnstoffe mit herbizider Wirkung
DD145881A5 (de)	1981-01-14	Zusammensetzung zum regulieren des pflanzenwuchses
DE2812622C2 (de)	1986-10-30	(2,3-Dihydro-2,2-dimethyl-benzofuran-7-yl-oxy-N-methyl-carbamoyl)-(N'-alkyl-carbamoyl)-sulfide, Verfahren zu deren Herstellung und diese Verbindungen enthaltende insektizide Mittel
CH628017A5 (de)	1982-02-15	Verfahren zur herstellung der neuen verbindung n-(4-benzyloxyphenyl)-n'-methyl-n'-methoxyharnstoff.
DE1137259B (de)	1962-09-27	Selektive Bekaempfung von Fingerhirse
CH632997A5 (en)	1982-11-15	Plant growth regulator
DD152902A5 (de)	1981-12-16	Pflanzenwachstumsregulator
US4108632A (en)	1978-08-22	Use of phthalanilic acids to regulate the growth of corn plants
DE2539396C3 (de)	1979-10-25	Pestizide
DE3300056C2 (de)	1985-06-27	3-Nitrobenzolsulfonanilid-Derivate und diese enthaltende fungizide Mittel
DD144502A5 (de)	1980-10-22	Pflanzenwachstumsregulator
DE69904800T2 (de)	2003-05-15	N-Acetonylbenzamide enthaltende fungizide Zusammensetzungen
DD145219A5 (de)	1980-12-03	Pflanzenwuchsregulierendes mittel
DD145991A5 (de)	1981-01-21	Landwirtschaftlich verwendbare zusammensetzung
DD143848A5 (de)	1980-09-17	Mittel zur bekaempfung von pilzen
DE1955892C3 (de)	1980-05-22	Verwendung eines Benzylthiolcarbamates als Herbizid
EP0040310A2 (de)	1981-11-25	Fungizide, heterocyclisch substituierte Thioglykolsäureanilide, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
DE2348022A1 (de)	1975-04-03	Sulfonamid-zubereitungen fuer herbicide
DD145992A5 (de)	1981-01-21	Pflanzenwachstumsregulator
AT389801B (de)	1990-02-12	Mittel zur bekaempfung von phytopathogenen pilzen
EP0092632B1 (de)	1985-09-04	Neue Benzonitrilderivate, Verfahren zu ihrer Herstellung und herbicide Mittel