CS214840B2 - Means for regulation of the plant growth and method of making the active substance - Google Patents

Means for regulation of the plant growth and method of making the active substance Download PDF

Info

Publication number: CS214840B2
Authority: CS; Czechoslovakia
Prior art keywords: growth; plant; plants; amount; plant growth
Prior art date: 1979-08-23

Application number

CS805769A

Other languages

Czech (cs)

English (en)

Inventor

Amico John J D

John T Marvel

Original Assignee

Monsanto Co

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

1982-06-25

1980-08-22 Application filed by Monsanto Co filed Critical Monsanto Co

1982-06-25 Publication of CS214840B2 publication Critical patent/CS214840B2/cs

Links

239000013543 active substance Substances 0.000 title claims description 3
230000008635 plant growth Effects 0.000 title abstract description 9
238000004519 manufacturing process Methods 0.000 title abstract description 3
150000001875 compounds Chemical class 0.000 claims abstract description 20
239000000203 mixture Substances 0.000 claims abstract description 15
230000012010 growth Effects 0.000 claims abstract description 12
238000000034 method Methods 0.000 claims abstract description 10
229910052736 halogen Inorganic materials 0.000 claims abstract description 5
150000002367 halogens Chemical group 0.000 claims abstract description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 4
229910052760 oxygen Inorganic materials 0.000 claims abstract description 4
239000001301 oxygen Substances 0.000 claims abstract description 4
230000008569 process Effects 0.000 claims abstract description 4
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N methyl cyanide Natural products CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 12
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 claims description 6
229910052717 sulfur Chemical group 0.000 claims description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 4
239000011593 sulfur Chemical group 0.000 claims description 4
239000000969 carrier Substances 0.000 claims description 3
239000003085 diluting agent Substances 0.000 claims description 3
-1 acetonitrile compound Chemical class 0.000 claims description 2
230000001105 regulatory effect Effects 0.000 abstract description 5
NOAJSOXBXNFQHP-UHFFFAOYSA-N 2-(2-oxo-1,3-benzothiazol-3-yl)ethanimidamide Chemical class C1=CC=C2SC(=O)N(CC(=N)N)C2=C1 NOAJSOXBXNFQHP-UHFFFAOYSA-N 0.000 abstract description 3
241000196324 Embryophyta Species 0.000 description 33
230000004048 modification Effects 0.000 description 13
238000012986 modification Methods 0.000 description 13
239000004480 active ingredient Substances 0.000 description 9
230000000694 effects Effects 0.000 description 9
230000005764 inhibitory process Effects 0.000 description 8
235000021374 legumes Nutrition 0.000 description 8
244000068988 Glycine max Species 0.000 description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 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
239000007788 liquid Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000000126 substance 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
239000003795 chemical substances by application Substances 0.000 description 4
230000001276 controlling effect Effects 0.000 description 4
230000000051 modifying effect Effects 0.000 description 4
239000002689 soil Substances 0.000 description 4
239000002904 solvent 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
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
230000018109 developmental process Effects 0.000 description 3
235000013399 edible fruits Nutrition 0.000 description 3
239000003630 growth substance Substances 0.000 description 3
239000005648 plant growth regulator Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000001953 recrystallisation Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-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
230000008859 change Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
230000003247 decreasing effect Effects 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000945 filler Substances 0.000 description 2
230000002015 leaf growth Effects 0.000 description 2
230000017066 negative regulation of growth Effects 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
235000021251 pulses Nutrition 0.000 description 2
230000026267 regulation of growth Effects 0.000 description 2
239000007921 spray 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
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
BCIJDSPGUOFPAI-UHFFFAOYSA-N 2-(2-sulfanylidene-1,3-benzothiazol-3-yl)acetonitrile Chemical class C1=CC=C2N(CC#N)C(=S)SC2=C1 BCIJDSPGUOFPAI-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-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
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 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
230000000996 additive effect Effects 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
150000001412 amines Chemical class 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
150000007514 bases Chemical class 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
235000014633 carbohydrates Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000004927 clay Substances 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
239000006185 dispersion Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation 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
230000004345 fruit ripening Effects 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
230000002363 herbicidal effect Effects 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
208000006278 hypochromic anemia Diseases 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
230000035800 maturation Effects 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002844 melting Methods 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
239000003960 organic solvent Substances 0.000 description 1
239000011236 particulate material Substances 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
230000008121 plant development 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
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000008262 pumice Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000004044 response Effects 0.000 description 1
230000000979 retarding effect Effects 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
230000007480 spreading Effects 0.000 description 1
238000003892 spreading Methods 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
230000000007 visual effect Effects 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)
Thiazole And Isothizaole Compounds (AREA)
Cultivation Of Plants (AREA)

CS805769A 1979-08-23 1980-08-22 Means for regulation of the plant growth and method of making the active substance CS214840B2 (en)

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
CS214840B2 true CS214840B2 (en)	1982-06-25

Family

ID=22086018

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS805769A CS214840B2 (en)	1979-08-23	1980-08-22	Means for regulation of the plant growth and method of making the active substance

Country Status (20)

Country	Link
US (1)	US4283220A (de)
EP (1)	EP0024889A1 (de)
JP (1)	JPS5677270A (de)
KR (1)	KR840001933B1 (de)
AR (1)	AR224418A1 (de)
AU (1)	AU530437B2 (de)
BG (1)	BG31502A3 (de)
BR (1)	BR8005341A (de)
CA (1)	CA1148959A (de)
CS (1)	CS214840B2 (de)
DD (1)	DD152902A5 (de)
DK (1)	DK361480A (de)
FI (1)	FI802660A7 (de)
IL (1)	IL60895A (de)
IN (1)	IN153446B (de)
NO (1)	NO802503L (de)
NZ (1)	NZ194736A (de)
PL (1)	PL226365A1 (de)
YU (1)	YU202580A (de)
ZA (1)	ZA805182B (de)

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
NL244642A (de) *	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 (de) *	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 AR AR282243A patent/AR224418A1/es active
- 1980-08-21 EP EP80302897A patent/EP0024889A1/de not_active Withdrawn
- 1980-08-21 KR KR1019800003304A patent/KR840001933B1/ko not_active Expired
- 1980-08-22 ZA ZA00805182A patent/ZA805182B/xx unknown
- 1980-08-22 CA CA000358958A patent/CA1148959A/en not_active Expired
- 1980-08-22 IN IN963/CAL/80A patent/IN153446B/en unknown
- 1980-08-22 NZ NZ194736A patent/NZ194736A/xx unknown
- 1980-08-22 CS CS805769A patent/CS214840B2/cs unknown
- 1980-08-22 IL IL60895A patent/IL60895A/xx unknown
- 1980-08-22 FI FI802660A patent/FI802660A7/fi not_active Application Discontinuation
- 1980-08-22 PL PL22636580A patent/PL226365A1/xx unknown
- 1980-08-22 BG BG048910A patent/BG31502A3/xx unknown
- 1980-08-22 JP JP11488080A patent/JPS5677270A/ja active Pending
- 1980-08-22 BR BR8005341A patent/BR8005341A/pt unknown
- 1980-08-22 DK DK361480A patent/DK361480A/da not_active Application Discontinuation
- 1980-08-22 DD DD80223460A patent/DD152902A5/de unknown
- 1980-08-22 AU AU61679/80A patent/AU530437B2/en not_active Ceased
- 1980-08-22 NO NO802503A patent/NO802503L/no unknown

Also Published As

Publication number	Publication date
PL226365A1 (de)	1981-06-05
EP0024889A1 (de)	1981-03-11
AU6167980A (en)	1981-03-05
JPS5677270A (en)	1981-06-25
KR830003451A (ko)	1983-06-20
US4283220A (en)	1981-08-11
NZ194736A (en)	1983-02-15
AR224418A1 (es)	1981-11-30
CA1148959A (en)	1983-06-28
IL60895A (en)	1983-11-30
ZA805182B (en)	1981-09-30
AU530437B2 (en)	1983-07-14
IN153446B (de)	1984-07-14
KR840001933B1 (ko)	1984-10-25
FI802660A7 (fi)	1981-02-23
YU202580A (en)	1983-04-30
BR8005341A (pt)	1981-03-04
IL60895A0 (en)	1980-10-26
BG31502A3 (bg)	1982-01-15
DK361480A (da)	1981-02-24
NO802503L (no)	1981-02-24
DD152902A5 (de)	1981-12-16

Publication	Publication Date	Title
EP0007161B1 (de)	1981-10-21	N-substituierte 2-Oxo-3-benzothiazolin-Derivate, ihre Verwendung zur Regulation des Wachstums von Leguminosen und diese Derivate als aktive Wirkstoffe enthaltende Zubereitungen zur Regulierung des Pflanzenwachstums
HU184615B (en)	1984-09-28	Compositions with antidote activity and process for preparing oxime derivatives applied as active substances thereof
US4006007A (en)	1977-02-01	N-(Substituted phenyl) derivatives of saccharin
EP0006347A1 (de)	1980-01-09	Zusammensetzungen und Verfahren zur Pflanzenwuchsregulierung von Sojabohnen durch Verwendung von substituierten Benzazolylthioalkansäuren
EP0007772B1 (de)	1983-09-07	N-substituierte Benzothiazoline und Benzoxazoline und ihre Anwendung als Herbizide und pflanzenwuchsregulierende Mittel
US4427436A (en)	1984-01-24	N-Substituted xanthate benzothiazoline and related derivatives
US4371388A (en)	1983-02-01	3-Substituted aminoalkyl-2-benzothiazolinones as plant growth regulants
US4289886A (en)	1981-09-15	Imides derived from 2-thioxo-3-benzox(thia)azoline acetic, and propionic acids
CS204956B2 (en)	1981-04-30	Regulator of the legumes growth
CS214840B2 (en)	1982-06-25	Means for regulation of the plant growth and method of making the active substance
US4185990A (en)	1980-01-29	Imides derived from 2-oxo-3-benzothiazolineacetic acid and butyric acid
US4187097A (en)	1980-02-05	N-hydrazides of 2-benzothiazolinone as plant growth regulants
US4578477A (en)	1986-03-25	N-substituted benzothiazoline and N-substituted benzoxazoline derivatives
EP0002932B1 (de)	1982-09-01	Verwendung von N-Substituierten Oxobenzothiazolinen als Pflanzenwachstumsregulatoren und N-Substituierten Oxobenzothiazolinen enthaltende Zusammensetzungen zur Regulierung des Pflanzenwachstums
US4308052A (en)	1981-12-29	N-Substituted benzothiazolines substituted with thiol esters useful as herbicides and plant growth regulants
EP0007162B1 (de)	1982-07-14	N-substituierte 2-Oxo-3-benzothiazolin-Derivate, ihre Verwendung zur Regulation des Wachstums von Leguminosen und diese Derivate als aktive Wirkstoffe enthaltende Zubereitungen zur Regulierung des Pflanzenwachstums
US4149871A (en)	1979-04-17	Alkylthioalkyl esters of 2-oxo-3-benzothiazolineacetic acid as plant growth regulators
US4422865A (en)	1983-12-27	Imides derived from 2-thioxo-3-(benzox (thia) azoline acetic and propionic acids
US4323686A (en)	1982-04-06	Benzothiazoleethanimidamides
US4323677A (en)	1982-04-06	N-Amides of 2-benzothiazolinone
KR810000835B1 (ko)	1981-08-07	피라졸 유도체의 제법
EP0022353A1 (de)	1981-01-14	2-Thioxo-3-benzothiazolin-acetonitril-Derivate, Verfahren zu ihrer Herstellung und ihre Anwendung als Mittel zur Regulation des Wachstums von Leguminosen