CS208499B2 - Means for regulation of the plants growth,particularly the vegetables - Google Patents

Means for regulation of the plants growth,particularly the vegetables Download PDF

Info

Publication number: CS208499B2
Authority: CS; Czechoslovakia
Prior art keywords: plants; growth; formula; plant; compounds
Prior art date: 1978-05-18

Application number

CS793436A

Other languages

Czech (cs)

English (en)

Inventor

Amico John J D

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.)

1978-05-18

Filing date

1979-05-17

Publication date

1981-09-15

1979-05-17 Application filed by Monsanto Co filed Critical Monsanto Co

1981-09-15 Publication of CS208499B2 publication Critical patent/CS208499B2/cs

Links

230000012010 growth Effects 0.000 title claims description 22
235000013311 vegetables Nutrition 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 45
239000000203 mixture Substances 0.000 claims abstract description 19
230000008635 plant growth Effects 0.000 claims abstract description 15
230000001105 regulatory effect Effects 0.000 claims abstract description 10
239000011591 potassium Substances 0.000 claims abstract description 7
229910052700 potassium Inorganic materials 0.000 claims abstract description 7
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 6
239000011734 sodium Substances 0.000 claims abstract description 3
229910052708 sodium Inorganic materials 0.000 claims abstract description 3
239000004480 active ingredient Substances 0.000 claims description 10
239000002671 adjuvant Substances 0.000 claims description 6
235000021374 legumes Nutrition 0.000 claims description 4
230000001276 controlling effect Effects 0.000 claims description 3
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 claims 1
101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 claims 1
208000003443 Unconsciousness Diseases 0.000 claims 1
150000001768 cations Chemical class 0.000 claims 1
101150035983 str1 gene Proteins 0.000 claims 1
238000002360 preparation method Methods 0.000 abstract description 6
-1 sodium cations Chemical class 0.000 abstract description 5
238000000034 method Methods 0.000 abstract description 3
241000196324 Embryophyta Species 0.000 description 62
208000006278 hypochromic anemia Diseases 0.000 description 21
244000068988 Glycine max Species 0.000 description 17
238000006243 chemical reaction Methods 0.000 description 15
238000012360 testing method Methods 0.000 description 15
235000010469 Glycine max Nutrition 0.000 description 11
KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 11
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
239000003630 growth substance Substances 0.000 description 10
238000009825 accumulation Methods 0.000 description 9
239000000126 substance Substances 0.000 description 9
230000009467 reduction Effects 0.000 description 8
239000004094 surface-active agent Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
238000011161 development Methods 0.000 description 7
230000005764 inhibitory process Effects 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
239000007788 liquid Substances 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 4
229920001213 Polysorbate 20 Polymers 0.000 description 4
230000000694 effects Effects 0.000 description 4
230000004048 modification Effects 0.000 description 4
238000012986 modification Methods 0.000 description 4
239000005648 plant growth regulator Substances 0.000 description 4
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 4
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 4
239000000047 product Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
241000894007 species Species 0.000 description 4
238000003756 stirring Methods 0.000 description 4
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-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
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000013543 active substance Substances 0.000 description 3
235000013399 edible fruits Nutrition 0.000 description 3
239000007921 spray Substances 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
BGPJLYIFDLICMR-UHFFFAOYSA-N 1,4,2,3-dioxadithiolan-5-one Chemical compound O=C1OSSO1 BGPJLYIFDLICMR-UHFFFAOYSA-N 0.000 description 2
LLKFNPUXQZHIAE-UHFFFAOYSA-N 5-(3-aminopropyl)-8-bromo-3-methyl-2h-pyrazolo[4,3-c]quinolin-4-one Chemical compound O=C1N(CCCN)C2=CC=C(Br)C=C2C2=C1C(C)=NN2 LLKFNPUXQZHIAE-UHFFFAOYSA-N 0.000 description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical group [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 2
241001464837 Viridiplantae Species 0.000 description 2
230000001133 acceleration Effects 0.000 description 2
239000002253 acid Substances 0.000 description 2
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
230000008901 benefit Effects 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
239000000969 carrier Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
239000000945 filler Substances 0.000 description 2
235000013312 flour Nutrition 0.000 description 2
235000013305 food Nutrition 0.000 description 2
230000002015 leaf growth Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
239000004033 plastic Substances 0.000 description 2
235000021251 pulses Nutrition 0.000 description 2
150000003839 salts Chemical group 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
VNDWQCSOSCCWIP-UHFFFAOYSA-N 2-tert-butyl-9-fluoro-1,6-dihydrobenzo[h]imidazo[4,5-f]isoquinolin-7-one Chemical compound C1=2C=CNC(=O)C=2C2=CC(F)=CC=C2C2=C1NC(C(C)(C)C)=N2 VNDWQCSOSCCWIP-UHFFFAOYSA-N 0.000 description 1
WBUHYKDOHNEIEL-UHFFFAOYSA-N 3-(2-hydroxyethyl)-1,3-benzothiazol-2-one Chemical compound C1=CC=C2SC(=O)N(CCO)C2=C1 WBUHYKDOHNEIEL-UHFFFAOYSA-N 0.000 description 1
241000218999 Begoniaceae Species 0.000 description 1
229910014033 C-OH Inorganic materials 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
101710178035 Chorismate synthase 2 Proteins 0.000 description 1
240000005109 Cryptomeria japonica Species 0.000 description 1
101710152694 Cysteine synthase 2 Proteins 0.000 description 1
229910014570 C—OH Inorganic materials 0.000 description 1
240000006497 Dianthus caryophyllus Species 0.000 description 1
235000009355 Dianthus caryophyllus Nutrition 0.000 description 1
241000218218 Ficus <angiosperm> Species 0.000 description 1
235000008730 Ficus carica Nutrition 0.000 description 1
239000004471 Glycine Substances 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
229920001214 Polysorbate 60 Polymers 0.000 description 1
NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
241000208422 Rhododendron Species 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 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
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
239000013011 aqueous formulation Substances 0.000 description 1
230000028446 budding cell bud growth Effects 0.000 description 1
230000008859 change Effects 0.000 description 1
230000009194 climbing Effects 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000007799 cork Substances 0.000 description 1
244000038559 crop plants Species 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
239000008187 granular material Substances 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
230000036541 health Effects 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
239000012535 impurity Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
210000000050 mohair Anatomy 0.000 description 1
150000004682 monohydrates Chemical class 0.000 description 1
230000017066 negative regulation of growth Effects 0.000 description 1
239000008188 pellet Substances 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
230000029553 photosynthesis Effects 0.000 description 1
238000010672 photosynthesis Methods 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000005080 plant death Effects 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000008569 process Effects 0.000 description 1
230000000750 progressive effect Effects 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000002786 root growth Effects 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
230000001052 transient effect Effects 0.000 description 1
230000007306 turnover Effects 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
238000012795 verification Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1
238000004383 yellowing Methods 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof

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)
Plural Heterocyclic Compounds (AREA)
Thiazole And Isothizaole Compounds (AREA)

CS793436A 1978-05-18 1979-05-17 Means for regulation of the plants growth,particularly the vegetables CS208499B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/907,390 US4171213A (en)	1978-05-18	1978-05-18	N-substituted oxybenzothiazoline derivatives and their use as plant growth regulants

Publications (1)

Publication Number	Publication Date
CS208499B2 true CS208499B2 (en)	1981-09-15

Family

ID=25424017

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS793436A CS208499B2 (en)	1978-05-18	1979-05-17	Means for regulation of the plants growth,particularly the vegetables

Country Status (17)

Country	Link
US (1)	US4171213A (es)
EP (1)	EP0007162B1 (es)
JP (1)	JPS54151967A (es)
AR (1)	AR219599A1 (es)
AU (1)	AU519082B2 (es)
BG (1)	BG34450A3 (es)
BR (1)	BR7903069A (es)
CA (1)	CA1124243A (es)
CS (1)	CS208499B2 (es)
DD (1)	DD145219A5 (es)
DE (1)	DE2963333D1 (es)
DK (1)	DK203779A (es)
IL (1)	IL57317A (es)
IT (1)	IT1114223B (es)
PL (1)	PL115427B1 (es)
SU (1)	SU833141A3 (es)
ZA (1)	ZA792418B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4427436A (en)	1982-07-12	1984-01-24	Monsanto Company	N-Substituted xanthate benzothiazoline and related derivatives
RU2013133873A (ru)	2010-12-21	2015-01-27	БАЙЕР КРОПСАЙЕНС ЭлПи	ШЕРОХОВАТЫЕ МУТАНТЫ Bacillus И СПОСОБЫ ИХ ПРИМЕНЕНИЯ ДЛЯ УСКОРЕНИЯ РОСТА РАСТЕНИЙ, УЛУЧШЕНИЯ ЗДОРОВЬЯ РАСТЕНИЙ И БОРЬБЫ С БОЛЕЗНЯМИ И ВРЕДИТЕЛЯМИ
BR112014005654A2 (pt)	2011-09-12	2017-03-28	Bayer Cropscience Lp	métodos para melhorar a saúde e promover o crescimento de uma planta e/ou de melhorar o amadurecimento da fruta

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB554756A (en) *	1941-02-26	1943-07-19	Monsanto Chemicals	Improvements in or relating to the vulcanization of rubber and accelerators therefor
NL108409C (es) *	1958-10-29
US3050526A (en) *	1960-08-08	1962-08-21	Rohm & Haas	3-thiocyanomethyl-2-benzothiazolinones and benzoxazolinones
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

1978
- 1978-05-18 US US05/907,390 patent/US4171213A/en not_active Expired - Lifetime
1979
- 1979-05-16 DE DE7979300850T patent/DE2963333D1/de not_active Expired
- 1979-05-16 EP EP79300850A patent/EP0007162B1/en not_active Expired
- 1979-05-17 IL IL57317A patent/IL57317A/xx unknown
- 1979-05-17 IT IT22761/79A patent/IT1114223B/it active
- 1979-05-17 CA CA327,945A patent/CA1124243A/en not_active Expired
- 1979-05-17 PL PL1979215665A patent/PL115427B1/pl unknown
- 1979-05-17 DK DK203779A patent/DK203779A/da unknown
- 1979-05-17 AR AR276557A patent/AR219599A1/es active
- 1979-05-17 AU AU47145/79A patent/AU519082B2/en not_active Ceased
- 1979-05-17 ZA ZA792418A patent/ZA792418B/xx unknown
- 1979-05-17 BG BG043623A patent/BG34450A3/xx unknown
- 1979-05-17 DD DD79212963A patent/DD145219A5/de unknown
- 1979-05-17 SU SU792766256A patent/SU833141A3/ru active
- 1979-05-17 JP JP5980279A patent/JPS54151967A/ja active Pending
- 1979-05-17 BR BR7903069A patent/BR7903069A/pt unknown
- 1979-05-17 CS CS793436A patent/CS208499B2/cs unknown

Also Published As

Publication number	Publication date
DE2963333D1 (en)	1982-09-02
BG34450A3 (en)	1983-09-15
JPS54151967A (en)	1979-11-29
EP0007162B1 (en)	1982-07-14
IT1114223B (it)	1986-01-27
DK203779A (da)	1979-11-19
IL57317A0 (en)	1979-09-30
US4171213A (en)	1979-10-16
AU519082B2 (en)	1981-11-05
DD145219A5 (de)	1980-12-03
AU4714579A (en)	1979-11-22
ZA792418B (en)	1980-06-25
BR7903069A (pt)	1979-12-04
IL57317A (en)	1981-06-29
SU833141A3 (ru)	1981-05-23
EP0007162A1 (en)	1980-01-23
CA1124243A (en)	1982-05-25
IT7922761A0 (it)	1979-05-17
AR219599A1 (es)	1980-08-29
PL215665A1 (es)	1980-03-24
PL115427B1 (en)	1981-04-30

Publication	Publication Date	Title
US4943309A (en)	1990-07-24	Method of defoleating cotton plants employing 3-carbonylphenyl uracil derivatives
US4049419A (en)	1977-09-20	Use of benzothiazoline compounds as plant growth regulants
HU182942B (en)	1984-03-28	Antidote and herbicide compositions containing oxyme derivatives and process for preparing the antidote
JPS5811422B2 (ja)	1983-03-02	１−アミノ−シクロプロパン−カルボン酸化合物の製造方法
EP0007161B1 (en)	1981-10-21	Novel n-substituted 2-oxo-3-benzothiazoline derivatives, their use as leguminous plant growth regulants, and plant growth regulating compositions containing said derivatives as the active ingredients
HU184615B (en)	1984-09-28	Compositions with antidote activity and process for preparing oxime derivatives applied as active substances thereof
US4108627A (en)	1978-08-22	N-(substituted phenyl) derivatives of saccharin
US3829306A (en)	1974-08-13	Plant regulation with 2-halo-2',6'-disubstituted-n-amidomethyl-acetanilides
US4066435A (en)	1978-01-03	Plant growth regulators
CS214672B2 (en)	1982-05-28	Means for regulation of the plant growth and insecticide means and method of making the active substances
JPS6317056B2 (es)	1988-04-12
HU182905B (en)	1984-03-28	Compositions for the plant growth regulation containing substituted benzazolyl-thio-alkancarboxylic acid derivatives
US4427436A (en)	1984-01-24	N-Substituted xanthate benzothiazoline and related derivatives
CS230598B2 (en)	1984-08-13	Fungicid agent and for regulation of growing of plants and method manufacture of efficient compound
US5176735A (en)	1993-01-05	Method of desiccating plants employing 3-carbonylphenyl uracil derivatives
CS208499B2 (en)	1981-09-15	Means for regulation of the plants growth,particularly the vegetables
EP0088066A1 (en)	1983-09-07	3,5-Bis (trifluoromethyl) phenoxy carboxylic acids and derivatives thereof
KR830001038B1 (ko)	1983-05-27	1, 3-디티오 복소환 화합물을 함유하는 제초제 조성물
CS208666B2 (en)	1981-09-15	Herbicide means and means for regulation of the plants growth
US4185990A (en)	1980-01-29	Imides derived from 2-oxo-3-benzothiazolineacetic acid and butyric acid
US4164406A (en)	1979-08-14	Phosphinylphthalimidines and their use as plant growth regulants
EP0001349B1 (en)	1981-02-11	N-substituted benzothiazolones and their use as herbicides and plant growth regulators
EP0002932B1 (en)	1982-09-01	The use of n-substituted oxobenzothiazolines as plant growth regulators and plant growth regulating compositions containing n-substituted oxobenzothiazolines
US3992185A (en)	1976-11-16	Dithio and thiol carbamates as plant growth regulants
CS214799B2 (cs)	1982-05-28	Prostředek k regulaci růstu rostlin a způsob výroby účinných látek