DD202097A5 - Formulierung zur selektiven bekaempfung von schaedlichen graesern und breitblaettrigen unkraeutern - Google Patents

Formulierung zur selektiven bekaempfung von schaedlichen graesern und breitblaettrigen unkraeutern Download PDF

Info

Publication number: DD202097A5
Authority: DD; German Democratic Republic
Prior art keywords: formulation; harmful; herbicide; selective control; uncraft
Prior art date: 1980-08-04

Application number

DD81232270A

Other languages

German (de)

English (en)

Inventor

Natu R Patel

Original Assignee

Gulf Oil Corp

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.)

1980-08-04

Filing date

1981-07-31

Publication date

1983-08-31

1981-07-31 Application filed by Gulf Oil Corp filed Critical Gulf Oil Corp

1983-08-31 Publication of DD202097A5 publication Critical patent/DD202097A5/de

Links

239000000203 mixture Substances 0.000 title claims description 9
238000009472 formulation Methods 0.000 title claims description 6
241000196324 Embryophyta Species 0.000 claims abstract description 15
241000209504 Poaceae Species 0.000 claims abstract description 7
240000006240 Linum usitatissimum Species 0.000 claims abstract description 6
235000004431 Linum usitatissimum Nutrition 0.000 claims abstract description 6
235000007319 Avena orientalis Nutrition 0.000 claims abstract description 5
244000075850 Avena orientalis Species 0.000 claims abstract description 5
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims abstract description 5
240000005979 Hordeum vulgare Species 0.000 claims abstract description 4
235000007340 Hordeum vulgare Nutrition 0.000 claims abstract description 4
235000021536 Sugar beet Nutrition 0.000 claims abstract description 4
240000002791 Brassica napus Species 0.000 claims abstract description 3
235000006008 Brassica napus var napus Nutrition 0.000 claims abstract description 3
239000004480 active ingredient Substances 0.000 claims description 3
239000000546 pharmaceutical excipient Substances 0.000 claims 2
QITOJKCIHXKJCG-UHFFFAOYSA-N 3-benzylsulfonyl-n,n-diethyl-1,2,4-triazole-1-carboxamide Chemical compound CCN(CC)C(=O)N1C=NC(S(=O)(=O)CC=2C=CC=CC=2)=N1 QITOJKCIHXKJCG-UHFFFAOYSA-N 0.000 claims 1
239000004009 herbicide Substances 0.000 abstract description 23
230000002363 herbicidal effect Effects 0.000 abstract description 18
150000001875 compounds Chemical class 0.000 abstract description 8
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
238000002360 preparation method Methods 0.000 description 7
239000000047 product Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
239000004094 surface-active agent Substances 0.000 description 5
-1 benzylsulfonyl compounds Chemical class 0.000 description 4
239000008187 granular material Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000013078 crystal Substances 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
238000000034 method Methods 0.000 description 3
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
239000002689 soil Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
150000003852 triazoles Chemical class 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
240000006122 Chenopodium album Species 0.000 description 2
235000009344 Chenopodium album Nutrition 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000000969 carrier Substances 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
239000004927 clay Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
RBBOWEDMXHTEPA-UHFFFAOYSA-N hexane;toluene Chemical compound CCCCCC.CC1=CC=CC=C1 RBBOWEDMXHTEPA-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000001953 recrystallisation Methods 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
QWENRTYMTSOGBR-UHFFFAOYSA-N 1H-1,2,3-Triazole Chemical compound C=1C=NNN=1 QWENRTYMTSOGBR-UHFFFAOYSA-N 0.000 description 1
JPQPSCZRSYIJIJ-UHFFFAOYSA-N 5-benzylsulfonyl-1h-1,2,4-triazole Chemical compound N=1C=NNC=1S(=O)(=O)CC1=CC=CC=C1 JPQPSCZRSYIJIJ-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
244000105624 Arachis hypogaea Species 0.000 description 1
241000209200 Bromus Species 0.000 description 1
241001148727 Bromus tectorum Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241000209082 Lolium Species 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
235000012629 Mentha aquatica Nutrition 0.000 description 1
240000000275 Persicaria hydropiper Species 0.000 description 1
235000017337 Persicaria hydropiper Nutrition 0.000 description 1
235000004442 Polygonum persicaria Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
238000013019 agitation Methods 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
244000038559 crop plants Species 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000007423 decrease Effects 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
CRPOUZQWHJYTMS-UHFFFAOYSA-N dialuminum;magnesium;disilicate Chemical compound [Mg+2].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] CRPOUZQWHJYTMS-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
239000003759 ester based solvent Substances 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
239000005457 ice water Substances 0.000 description 1
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 1
239000010410 layer Substances 0.000 description 1
235000019357 lignosulphonate Nutrition 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
OFCCYDUUBNUJIB-UHFFFAOYSA-N n,n-diethylcarbamoyl chloride Chemical compound CCN(CC)C(Cl)=O OFCCYDUUBNUJIB-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
150000002895 organic esters Chemical class 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
239000012254 powdered material Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
241001478887 unidentified soil bacteria Species 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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 to ring carbon atoms
- C07D249/12—Oxygen or 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)
Plural Heterocyclic Compounds (AREA)

DD81232270A 1980-08-04 1981-07-31 Formulierung zur selektiven bekaempfung von schaedlichen graesern und breitblaettrigen unkraeutern DD202097A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/174,975 US4280831A (en)	1980-08-04	1980-08-04	Benzylsulfonyl diethylcarbamyl triazole and use as a selective herbicide

Publications (1)

Publication Number	Publication Date
DD202097A5 true DD202097A5 (de)	1983-08-31

Family

ID=22638300

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD81232270A DD202097A5 (de)	1980-08-04	1981-07-31	Formulierung zur selektiven bekaempfung von schaedlichen graesern und breitblaettrigen unkraeutern

Country Status (10)

Country	Link
US (1)	US4280831A (ja)
EP (1)	EP0045566A3 (ja)
JP (1)	JPS5758675A (ja)
AR (1)	AR227553A1 (ja)
AU (1)	AU7301181A (ja)
BR (1)	BR8104837A (ja)
DD (1)	DD202097A5 (ja)
DE (1)	DE3129428A1 (ja)
ES (1)	ES8305339A1 (ja)
ZA (1)	ZA814792B (ja)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3316300A1 (de) *	1982-05-07	1983-11-24	Kureha Kagaku Kogyo K.K., Tokyo	Heribizide zusammensetzung mit einem gehalt an einem derivat des 1,2,4-triazols als wirkstoff
CA1225399A (en) *	1983-10-18	1987-08-11	Ryo Yoshida	Carbamoyltriazoles, and their production and use
JP2556683B2 (ja)	1986-07-04	1996-11-20	住友化学工業株式会社	カルバモイルトリアゾール誘導体およびそれを有効成分とする除草剤
JPH0778045B2 (ja) *	1987-03-19	1995-08-23	呉羽化学工業株式会社	１，５−ジフエニル−１ｈ−１，２，４−トリアゾ−ル−３−カルボン酸アミド誘導体及び該誘導体を含有する除草剤
US5147445A (en) *	1988-03-07	1992-09-15	Chugai Seiyaku Kabushiki Kaisha	Herbicidal triazole compounds and herbicidal compositions containing the same
DE68917617T2 (de) *	1988-03-07	1994-12-22	Chugai Pharmaceutical Co Ltd	Triazolverbindungen, Verfahren zu ihrer Herstellung und diese enthaltende herbizide Zusammensetzungen.
DE3929673A1 (de) *	1989-09-07	1991-03-14	Bayer Ag	Substituierte carbamoyltriazole
ES2124705T3 (es) *	1990-08-03	1999-02-16	Chugai Pharmaceutical Co Ltd	Compuesto de triazol.
JP3036841B2 (ja)	1990-08-03	2000-04-24	中外製薬株式会社	トリアゾール系化合物
US5258361A (en) *	1991-09-27	1993-11-02	Rohm And Haas Company	Herbicidal 1-(disubstituted carbamoyl)-3-(N-arylsulfonamido)-1,2,4-triazoles
US5211739A (en) *	1991-09-27	1993-05-18	Rohm And Haas Company	Herbicidal-1-(disubstituted carbamoyl or thiocarbamoyl)-1,2,4-triazol-3-yl sulfonates and thisulfonates
US6461997B1 (en)	1999-01-14	2002-10-08	Monsanto Technology Llc	Triazole sulfones having herbicidal activity

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3308131A (en) *	1962-12-06	1967-03-07	Du Pont	Tertiary carbamyl triazoles
GB1316280A (en) *	1970-07-01	1973-05-09	Boots Co Ltd	Herbicidal agents
US3952001A (en) *	1970-07-01	1976-04-20	The Boots Company Limited	1-Carbamoyl-1,2,4-triazoles
LU67908A1 (ja) *	1973-06-29	1973-08-31
DE2834879A1 (de) *	1978-08-07	1980-02-21	Schering Ag	1,2,3-triazolcarbonsaeureamide, verfahren zur herstellung dieser verbindungen sowie diese enthaltende biozide mittel

1980
- 1980-08-04 US US06/174,975 patent/US4280831A/en not_active Expired - Lifetime
1981
- 1981-07-06 EP EP81303061A patent/EP0045566A3/en not_active Withdrawn
- 1981-07-14 ZA ZA814792A patent/ZA814792B/xx unknown
- 1981-07-15 AU AU73011/81A patent/AU7301181A/en not_active Abandoned
- 1981-07-17 AR AR286126A patent/AR227553A1/es active
- 1981-07-25 DE DE19813129428 patent/DE3129428A1/de not_active Withdrawn
- 1981-07-28 BR BR8104837A patent/BR8104837A/pt unknown
- 1981-07-31 DD DD81232270A patent/DD202097A5/de unknown
- 1981-08-03 ES ES504503A patent/ES8305339A1/es not_active Expired
- 1981-08-03 JP JP56121768A patent/JPS5758675A/ja active Pending

Also Published As

Publication number	Publication date
ES504503A0 (es)	1982-11-01
ZA814792B (en)	1983-02-23
DE3129428A1 (de)	1982-06-03
EP0045566A3 (en)	1982-02-17
BR8104837A (pt)	1982-04-13
AR227553A1 (es)	1982-11-15
JPS5758675A (en)	1982-04-08
EP0045566A2 (en)	1982-02-10
AU7301181A (en)	1982-02-11
US4280831A (en)	1981-07-28
ES8305339A1 (es)	1982-11-01

Publication	Publication Date	Title
EP0083556A2 (de)	1983-07-13	Alpha-(4-(3'-Fluor-5'-halogen-pyridyl-2'-oxy)-phenoxy)-propionsäure derivate mit herbizider Wirkung
DD202097A5 (de)	1983-08-31	Formulierung zur selektiven bekaempfung von schaedlichen graesern und breitblaettrigen unkraeutern
DE2428372C2 (de)	1985-07-25	Fluoralkoxyphenylsubstituierte Stickstoffheterozyklen, Verfahren zu deren Herstellung und diese Verbindungen enthaltende wachstumsinhibierende Zubereitung
EP0003805B1 (de)	1982-06-30	Pyridazonverbindungen und diese enthaltende herbizide Zusammensetzungen
DD232184A5 (de)	1986-01-22	Pestizide zusammensetzung
EP0071794A1 (de)	1983-02-16	5-Amino-1-phenyl-pyrazol-4-carbonsäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE68917617T2 (de)	1994-12-22	Triazolverbindungen, Verfahren zu ihrer Herstellung und diese enthaltende herbizide Zusammensetzungen.
DD253565A5 (de)	1988-01-27	Herbizide zusammensetzungen
EP0028829B1 (de)	1983-09-28	Harnstoffe mit cyclischen Substituenten, ihre Herstellung und Verwendung als Herbizide
DD262573A5 (de)	1988-12-07	Herbizide mittel
DE3107629C2 (de)	1987-01-08	2-Cyan-2-phenylacetamide und diese enthaltende pflanzenwachstumsregulierende Mittel
DE2619303A1 (de)	1976-11-18	Neue schwefelhaltige bisformamidine, verfahren zu ihrer herstellung und verwendung derselben sowie diese enthaltende land-, garten- und forstwirtschaftliche chemikalien
DE1667979C3 (de)	1978-06-01	13-Benzodioxolcarbamate sowie Verfahren zu deren Herstellung und Schädlingsbekämpfungsmittel mit einem Gehalt dieser Verbindungen
DE3533440A1 (de)	1987-03-26	N-substituierte 3,4,5,6-tetrahydrophthalimide, verfahren zu ihrer herstellung sowie ihre verwendung im pflanzenschutz
DE2711230A1 (de)	1977-09-29	N-(4-benzyloxyphenyl)-n'-methyl-n'- methoxyharnstoff, verfahren zu seiner herstellung und seine verwendung als herbizid insbesondere in sojabohnenkulturen
EP0001751B1 (de)	1980-09-17	N-(Imidazolylmethyl)-acetanilide, ihre Verwendung als Herbizide und Verfahren zur Bekämpfung unerwünschten Pflanzenwuchses
DD271447A5 (de)	1989-09-06	Verfahren zur regulierung des wachstums von pflanzen
EP0058639B1 (de)	1985-08-14	2-(4-(6-Halogen-chinoxalinyl-2-oxy)-phenoxy)-propionsäureester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Herbizide und Pflanzenwuchsregulatoren
DD210190A5 (de)	1984-06-06	Herbizides mittel
EP0053699A1 (de)	1982-06-16	2'-Phenylhydrazino-2-cyanacrylsäureester und diese enthaltende Herbizide
DE2650557A1 (de)	1977-05-12	Verfahren und mittel zur regulierung des wachstums und der entwicklung von pflanzen
EP0106114A2 (de)	1984-04-25	Phosphorhaltige funktionelle Essigsäurederivate, Verfahren zu ihrer Herstellung und sie enthaltende herbizide und wachstumsregulierende Mittel
DE69320104T2 (de)	1999-04-08	Furobenzopyranderivate, Verfahren zu ihrer Herstellung und Herbizide, die diese Derivate als aktive Komponenten enthalten
DD262992A5 (de)	1988-12-21	Nematizide und insektizide zusammensetzung
DE2012973C3 (de)	1978-09-28	Benzohydroximsäureesterverbindungen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende acarizide Mittel