CS235026B2 - Herbicide agent - Google Patents

Herbicide agent Download PDF

Info

Publication number: CS235026B2
Authority: CS; Czechoslovakia
Prior art keywords: compound; compounds; formula; active; formulas
Prior art date: 1981-09-17

Application number

CS826641A

Other languages

Czech (cs)

English (en)

Inventor

Hans Schumacher

Konrad Albrecht

Rudolf Heinrich

Original Assignee

Hoechst Ag

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.)

1981-09-17

Filing date

1982-09-15

Publication date

1985-04-16

1982-09-15 Application filed by Hoechst Ag filed Critical Hoechst Ag

1985-04-16 Publication of CS235026B2 publication Critical patent/CS235026B2/cs

Links

239000004009 herbicide Substances 0.000 title description 5
150000001875 compounds Chemical class 0.000 claims abstract description 52
239000000203 mixture Substances 0.000 claims abstract description 25
230000002363 herbicidal effect Effects 0.000 claims abstract description 12
125000000217 alkyl group Chemical group 0.000 claims abstract description 4
239000004480 active ingredient Substances 0.000 claims description 20
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
230000002195 synergetic effect Effects 0.000 abstract description 8
241000209504 Poaceae Species 0.000 abstract 1
150000001768 cations Chemical class 0.000 abstract 1
244000038559 crop plants Species 0.000 abstract 1
230000000694 effects Effects 0.000 description 15
241000196324 Embryophyta Species 0.000 description 12
239000013543 active substance Substances 0.000 description 10
-1 6-chloro-2-benzthiazolyloxy Chemical group 0.000 description 8
244000075850 Avena orientalis Species 0.000 description 8
GVOISEJVFFIGQE-YCZSINBZSA-N n-[(1r,2s,5r)-5-[methyl(propan-2-yl)amino]-2-[(3s)-2-oxo-3-[[6-(trifluoromethyl)quinazolin-4-yl]amino]pyrrolidin-1-yl]cyclohexyl]acetamide Chemical compound CC(=O)N[C@@H]1C[C@H](N(C)C(C)C)CC[C@@H]1N1C(=O)[C@@H](NC=2C3=CC(=CC=C3N=CN=2)C(F)(F)F)CC1 GVOISEJVFFIGQE-YCZSINBZSA-N 0.000 description 7
239000000843 powder Substances 0.000 description 7
235000007319 Avena orientalis Nutrition 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
239000004495 emulsifiable concentrate Substances 0.000 description 6
235000008515 Setaria glauca Nutrition 0.000 description 5
244000010062 Setaria pumila Species 0.000 description 5
229940125890 compound Ia Drugs 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
206010011878 Deafness Diseases 0.000 description 4
240000005979 Hordeum vulgare Species 0.000 description 4
238000009472 formulation Methods 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
235000007320 Avena fatua Nutrition 0.000 description 3
241000209764 Avena fatua Species 0.000 description 3
241000380130 Ehrharta erecta Species 0.000 description 3
235000007340 Hordeum vulgare Nutrition 0.000 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 description 3
241000209082 Lolium Species 0.000 description 3
244000100545 Lolium multiflorum Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
244000062793 Sorghum vulgare Species 0.000 description 3
239000000969 carrier Substances 0.000 description 3
235000013339 cereals Nutrition 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
230000001186 cumulative effect Effects 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
235000005781 Avena Nutrition 0.000 description 2
235000017896 Digitaria Nutrition 0.000 description 2
241001303487 Digitaria <clam> Species 0.000 description 2
244000152970 Digitaria sanguinalis Species 0.000 description 2
235000010823 Digitaria sanguinalis Nutrition 0.000 description 2
244000058871 Echinochloa crus-galli Species 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
235000011999 Panicum crusgalli Nutrition 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
235000011684 Sorghum saccharatum Nutrition 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
244000291564 Allium cepa Species 0.000 description 1
235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
240000004551 Drosera rotundifolia Species 0.000 description 1
235000008497 Drosera rotundifolia Nutrition 0.000 description 1
241000192043 Echinochloa Species 0.000 description 1
244000025670 Eleusine indica Species 0.000 description 1
235000014716 Eleusine indica Nutrition 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000060234 Gmelina philippensis Species 0.000 description 1
229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
241000526093 Hyla arborea Species 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
241001233957 eudicotyledons Species 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
239000000243 solution Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003860 storage Methods 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
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS826641A 1981-09-17 1982-09-15 Herbicide agent CS235026B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813136913 DE3136913A1 (de)	1981-09-17	1981-09-17	"herbizide mittel"

Publications (1)

Publication Number	Publication Date
CS235026B2 true CS235026B2 (en)	1985-04-16

Family

ID=6141900

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS826641A CS235026B2 (en)	1981-09-17	1982-09-15	Herbicide agent

Country Status (16)

Country	Link
US (1)	US4448602A (fr)
EP (1)	EP0075249B1 (fr)
AT (1)	ATE11723T1 (fr)
AU (1)	AU8844882A (fr)
BR (1)	BR8205428A (fr)
CS (1)	CS235026B2 (fr)
DD (1)	DD204023A5 (fr)
DE (2)	DE3136913A1 (fr)
GR (1)	GR77335B (fr)
IL (1)	IL66809A0 (fr)
MA (1)	MA19599A1 (fr)
PL (1)	PL130296B1 (fr)
PT (1)	PT75572A (fr)
SU (1)	SU1145907A3 (fr)
ZA (1)	ZA826794B (fr)
ZW (1)	ZW19382A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU192508B (en) *	1984-11-19	1987-06-29	Ferenc Tomonicska	Synergic herbicidal compositions comprising 5-(2,4-dichlorphenoxy)-2-nitro-benzoic acid methylester and 2,-/4-(6-chlor-2-benzoxazolyl)-oxy/-phenoxy-propionic acid-ethylester as active substance
DE3806294A1 (de) *	1988-02-27	1989-09-07	Hoechst Ag	Herbizide mittel in form von waessrigen mikroemulsionen
US4954161A (en) *	1989-01-09	1990-09-04	American Cyanamid Company	Herbicidal composition and method for safening gramineous crops against heterocyclic phenyl ethers

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3904396A (en) *	1971-03-23	1975-09-09	Schering Ag	Herbicidal mixture of several carbamoyloxyphenylcarbamates
DE2640730C2 (de) *	1976-09-10	1983-08-25	Hoechst Ag, 6230 Frankfurt	Benzoxazolyloxy- und Benzothiazolyloxy-phenoxy-Verbindungen und diese enthaltende herbizide Mittel
DE2745869A1 (de) *	1977-10-12	1979-04-19	Hoechst Ag	Herbizide mittel zur bekaempfung von ein- und mehrjaehrigen graesern
DE2815287A1 (de) *	1978-04-08	1979-10-18	Hoechst Ag	Herbizide mittel

1981
- 1981-09-17 DE DE19813136913 patent/DE3136913A1/de not_active Withdrawn
1982
- 1982-09-14 AT AT82108461T patent/ATE11723T1/de not_active IP Right Cessation
- 1982-09-14 DE DE8282108461T patent/DE3262339D1/de not_active Expired
- 1982-09-14 EP EP82108461A patent/EP0075249B1/fr not_active Expired
- 1982-09-15 CS CS826641A patent/CS235026B2/cs unknown
- 1982-09-15 US US06/418,396 patent/US4448602A/en not_active Expired - Fee Related
- 1982-09-15 ZW ZW193/82A patent/ZW19382A1/xx unknown
- 1982-09-15 GR GR69277A patent/GR77335B/el unknown
- 1982-09-15 DD DD82243272A patent/DD204023A5/de unknown
- 1982-09-16 BR BR8205428A patent/BR8205428A/pt unknown
- 1982-09-16 SU SU823493680A patent/SU1145907A3/ru active
- 1982-09-16 PT PT75572A patent/PT75572A/pt unknown
- 1982-09-16 MA MA19811A patent/MA19599A1/fr unknown
- 1982-09-16 AU AU88448/82A patent/AU8844882A/en not_active Abandoned
- 1982-09-16 PL PL1982238251A patent/PL130296B1/pl unknown
- 1982-09-16 ZA ZA826794A patent/ZA826794B/xx unknown
- 1982-09-16 IL IL66809A patent/IL66809A0/xx unknown

Also Published As

Publication number	Publication date
EP0075249B1 (fr)	1985-02-13
PT75572A (en)	1982-10-01
PL130296B1 (en)	1984-07-31
ZW19382A1 (en)	1983-04-20
US4448602A (en)	1984-05-15
DD204023A5 (de)	1983-11-16
ZA826794B (en)	1983-07-27
GR77335B (fr)	1984-09-11
DE3262339D1 (en)	1985-03-28
IL66809A0 (en)	1982-12-31
PL238251A1 (en)	1983-04-11
MA19599A1 (fr)	1983-04-01
ATE11723T1 (de)	1985-02-15
AU8844882A (en)	1983-03-24
EP0075249A1 (fr)	1983-03-30
BR8205428A (pt)	1983-08-23
SU1145907A3 (ru)	1985-03-15
DE3136913A1 (de)	1983-04-21

Publication	Publication Date	Title
DE69625587T2 (de)	2003-09-04	Synergistiche herbizide zusammensetzungen mit metolachlor
WO2004084632A1 (fr)	2004-10-07	Fongicides contenant un compose d'ester methyle d'acide acrylique methoxy
JPS63115803A (ja)	1988-05-20	稲作において選択的に雑草を防除するための相乗作用組成物
US4336057A (en)	1982-06-22	Herbicides
SU1556539A3 (ru)	1990-04-07	Способ получени замещенных 2-фенилиминооксазолидинонов-4
JPH06145006A (ja)	1994-05-24	除草剤組成物
US3954998A (en)	1976-05-04	Substituted phenyl indandiones as miticides
AU652298B2 (en)	1994-08-18	Synergistic composition and method of selective weed control
CS235026B2 (en)	1985-04-16	Herbicide agent
CA1329994C (fr)	1994-06-07	Melange herbicide et methode connexe assurant un controle selectif des mauvaises herbes
EP0296319B1 (fr)	1992-01-08	Agents herbicides à base de dérivés d'acides hétéroaryloxyphénoxycarboxyliques
CS221842B2 (en)	1983-04-29	Synergic means for selective destroying the weeds
US4589908A (en)	1986-05-20	Herbicidal agents
CA1164337A (fr)	1984-03-27	Melanges synergistes insecticides a base de phosphorothionate de 0,0-diethyle et de 0-(3,5,6- trichloro-2-pyridinyle), ainsi que de phosphorothionate de 0,0-dimethyle et de s-(n-methyl- carbamoylmethyle)
JPS60139666A (ja)	1985-07-24	イソチオ尿素、その製法およびその使用方法
JPS5841807A (ja)	1983-03-11	除草剤
GB2059418A (en)	1981-04-23	Pyroline derivatives and their use as acaricidal agents
HU213380B (en)	1997-05-28	Selective herbicidal composition
US4213975A (en)	1980-07-22	Insecticidal synergistic mixtures of O,O-diethyl O-(3,5,6-trichloro-2-pyridinyl)phosphorothioate and O-ethyl O-(4-(methylthio)phenyl)-S-n-propyl phosphorothioate
US4301155A (en)	1981-11-17	Insecticidal synergistic mixtures of O,O-diethyl O-(3,5,6-trichloro-2-pyridinyl)phosphorothioate and 2,2,3,3-tetramethylcyclopropanecarboxylic acid:cyano(3-phenoxyphenyl)methyl ester
CA1129341A (fr)	1982-08-10	Melanges synergistes insecticides de phosphorothioate de 0,0-diethyl 0-(3,5,6-trichloro-2-pyridinyl) et d'acide 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane carboxylique: cyano(6-phenoxy-2-pyridinyl)methyl ester
US2989391A (en)	1961-06-20	Method for modifying the growth characteristics of plants
JPS5815903A (ja)	1983-01-29	選択除草剤組成物及び選択的除草方法
US3397052A (en)	1968-08-13	Process for controlling plant life
KR810000691B1 (ko)	1981-06-22	1,8-디치환 카르보스티릴 유도체의 제조방법