DD202614A5 - Herbizide mittel - Google Patents

Herbizide mittel Download PDF

Info

Publication number: DD202614A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; atoms; triazines; fluorine; methyl
Prior art date: 1981-08-29

Application number

DD82242823A

Other languages

German (de)

English (en)

Inventor

Engelbert Kuehle

Bernd Baasner

Ludwig Eue

Robert R Schmidt

Hermann Hagemann

Original Assignee

Bayer 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.)

1981-08-29

Filing date

1982-08-26

Publication date

1983-09-28

1982-08-26 Application filed by Bayer Ag filed Critical Bayer Ag

1983-09-28 Publication of DD202614A5 publication Critical patent/DD202614A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 8
239000004009 herbicide Substances 0.000 title claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 23
239000000460 chlorine Substances 0.000 claims abstract description 17
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 16
239000011737 fluorine Substances 0.000 claims abstract description 16
229910052731 fluorine Inorganic materials 0.000 claims abstract description 16
239000001257 hydrogen Substances 0.000 claims abstract description 13
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 13
229910052801 chlorine Inorganic materials 0.000 claims abstract description 8
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 7
125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
125000003709 fluoroalkyl group Chemical group 0.000 claims abstract description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical class NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 claims abstract description 3
DUAJIKVIRGATIW-UHFFFAOYSA-N trinitrogen(.) Chemical compound [N]=[N+]=[N-] DUAJIKVIRGATIW-UHFFFAOYSA-N 0.000 claims abstract description 3
238000000034 method Methods 0.000 claims description 26
241000196324 Embryophyta Species 0.000 claims description 20
230000008569 process Effects 0.000 claims description 18
238000002360 preparation method Methods 0.000 claims description 10
239000004606 Fillers/Extenders Substances 0.000 claims description 4
239000004094 surface-active agent Substances 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
ZVIZHAICAJLHGZ-UHFFFAOYSA-N 2h-1,3,5-triazine-1,2-diamine Chemical compound NC1N=CN=CN1N ZVIZHAICAJLHGZ-UHFFFAOYSA-N 0.000 claims 2
239000000203 mixture Substances 0.000 abstract description 16
239000004480 active ingredient Substances 0.000 abstract description 13
125000004414 alkyl thio group Chemical group 0.000 abstract description 4
-1 unsaturated aliphatic radical Chemical class 0.000 description 31
150000001875 compounds Chemical class 0.000 description 25
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239000000243 solution Substances 0.000 description 17
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
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150000001412 amines Chemical class 0.000 description 13
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
239000002253 acid Substances 0.000 description 9
125000004435 hydrogen atom Chemical class [H]* 0.000 description 9
238000002844 melting Methods 0.000 description 9
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239000011230 binding agent Substances 0.000 description 8
125000000217 alkyl group Chemical group 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
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150000003918 triazines Chemical class 0.000 description 7
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238000009835 boiling Methods 0.000 description 4
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239000007868 Raney catalyst Substances 0.000 description 3
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239000000543 intermediate Substances 0.000 description 3
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150000003254 radicals Chemical class 0.000 description 3
150000003839 salts Chemical group 0.000 description 3
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229910052783 alkali metal Inorganic materials 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
150000004703 alkoxides Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
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125000000129 anionic group Chemical group 0.000 description 1
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239000008346 aqueous phase Substances 0.000 description 1
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GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
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239000002274 desiccant Substances 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
235000014113 dietary fatty acids Nutrition 0.000 description 1
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PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
VBKFRZZEICMFFH-UHFFFAOYSA-N n-(2,2,2-trifluoroethyl)butan-1-amine Chemical compound CCCCNCC(F)(F)F VBKFRZZEICMFFH-UHFFFAOYSA-N 0.000 description 1
KSUNPCLRJWKSHY-UHFFFAOYSA-N n-(2,2,2-trifluoroethyl)propan-1-amine Chemical compound CCCNCC(F)(F)F KSUNPCLRJWKSHY-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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235000014571 nuts Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
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125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
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239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
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239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
239000011435 rock Substances 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
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238000003892 spreading Methods 0.000 description 1
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238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000013616 tea Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1
235000014101 wine Nutrition 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/42—One nitrogen atom
- C07D251/44—One nitrogen atom with halogen atoms attached to the two other ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/48—Two nitrogen atoms
- C07D251/50—Two nitrogen atoms with a halogen atom attached to the third ring carbon atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/48—Two nitrogen atoms
- C07D251/52—Two nitrogen atoms with an oxygen or sulfur atom attached to the third ring carbon atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C07D251/70—Other substituted melamines

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)

DD82242823A 1981-08-29 1982-08-26 Herbizide mittel DD202614A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3134227		1981-08-29
DE3218966A DE3218966A1 (de)	1981-08-29	1982-05-19	Fluorhaltige 4,6-diamino-s-triazine, verfahren und neue zwischenprodukte zu ihrer herstellung und ihre verwendung als herbizide

Publications (1)

Publication Number	Publication Date
DD202614A5 true DD202614A5 (de)	1983-09-28

Family

ID=25795636

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82242823A DD202614A5 (de)	1981-08-29	1982-08-26	Herbizide mittel

Country Status (12)

Country	Link
US (1)	US4459151A (da)
EP (1)	EP0073974A3 (da)
AU (1)	AU8758682A (da)
BR (1)	BR8205024A (da)
DD (1)	DD202614A5 (da)
DE (1)	DE3218966A1 (da)
DK (1)	DK385282A (da)
ES (1)	ES8305743A1 (da)
IL (1)	IL66647A0 (da)
OA (1)	OA07198A (da)
PL (1)	PL238064A1 (da)
PT (1)	PT75445B (da)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3305201A1 (de) *	1983-02-16	1984-08-16	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von fluorierten nitroalkanen
JPS62126178A (ja) *	1985-11-26	1987-06-08	Mitsubishi Petrochem Co Ltd	新規トリアジン誘導体及びこれを含む除草剤
DE3611193A1 (de) *	1986-04-04	1987-10-15	Bayer Ag	N-substituierte benzamide
DE3611427A1 (de) *	1986-04-05	1987-10-08	Hoechst Ag	Bis-tertiaerbutylamino-substituierte 1,3,5-triazinderivate, verfahren zu ihrer herstellung, diese verbindungen enthaltende arzneimittel und ihre verwendung
DE3801113A1 (de) *	1987-07-23	1989-02-02	Bayer Ag	Substituierte triazine
DE4329598A1 (de) *	1993-09-02	1995-03-09	Bayer Ag	Malodinitril-substituierte 1,3,5-Triazin-diamine
IT1308639B1 (it) *	1999-03-03	2002-01-09	Ausimont Spa	Composti triazinici fluorurati.
WO2018095811A1 (en) *	2016-11-28	2018-05-31	Basf Se	Diaminotriazine compounds
CA3194093A1 (en) *	2022-03-23	2023-09-23	Foremark Performance Chemicals	Method and scavening mixture for removing hydrogen sulfide from a gas stream

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA674325A (en) *		1963-11-19	L. Wear Robert	Fluorocarbon-substituted triazines
US2141394A (en) *	1937-09-27	1938-12-27	Mesta Machine Co	Apparatus and method for handling sheetlike material
CH336223A (de) *	1955-01-14	1959-02-15	Geigy Ag J R	Verfahren und Mittel zur Beeinflussung des Pflanzenwachstums, insbesondere zur Bekämpfung von Unkraut
BE632365A (da) *	1962-05-15
DE1449253A1 (da) *	1964-10-06
DE1695117C3 (de) *	1968-02-09	1974-01-17	Ciba-Geigy Ag, Basel (Schweiz)	Verfahren zur Herstellung von Chloramino-s-triazinen
DE1770576A1 (de) *	1968-06-06	1971-11-04	Bayer Ag	Verfahren zur Herstellung von alpha-chlorierten Dialkyl- und Alkyl-arylamino-s-triazinen
US3494759A (en) *	1968-09-13	1970-02-10	Allied Chem	Triazine herbicides
CA962270A (en) *	1970-08-19	1975-02-04	Agripat S.A.	Alkoxy-methylamino-s-triazines
DE2425287A1 (de) *	1974-05-24	1975-12-11	Celamerck Gmbh & Co Kg	Triazinderivate

1982
- 1982-05-19 DE DE3218966A patent/DE3218966A1/de not_active Withdrawn
- 1982-08-13 US US06/408,082 patent/US4459151A/en not_active Expired - Fee Related
- 1982-08-18 EP EP82107513A patent/EP0073974A3/de not_active Withdrawn
- 1982-08-19 PT PT75445A patent/PT75445B/pt unknown
- 1982-08-25 AU AU87586/82A patent/AU8758682A/en not_active Abandoned
- 1982-08-26 OA OA57789A patent/OA07198A/xx unknown
- 1982-08-26 DD DD82242823A patent/DD202614A5/de unknown
- 1982-08-26 IL IL66647A patent/IL66647A0/xx unknown
- 1982-08-27 PL PL23806482A patent/PL238064A1/xx unknown
- 1982-08-27 ES ES515316A patent/ES8305743A1/es not_active Expired
- 1982-08-27 DK DK385282A patent/DK385282A/da unknown
- 1982-08-27 BR BR8205024A patent/BR8205024A/pt unknown

Also Published As

Publication number	Publication date
PT75445A (en)	1982-09-01
IL66647A0 (en)	1982-12-31
OA07198A (fr)	1984-04-30
DE3218966A1 (de)	1983-03-24
ES515316A0 (es)	1983-05-01
PT75445B (en)	1984-11-19
PL238064A1 (en)	1983-05-09
AU8758682A (en)	1983-03-10
ES8305743A1 (es)	1983-05-01
EP0073974A3 (de)	1983-11-16
US4459151A (en)	1984-07-10
EP0073974A2 (de)	1983-03-16
DK385282A (da)	1983-03-01
BR8205024A (pt)	1983-08-09

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DE4206531A1 (de)	1993-09-09	N-aryl-stickstoffheterocyclen
DD202614A5 (de)	1983-09-28	Herbizide mittel
DE4228000A1 (de)	1994-03-03	3-Aryl-triazin-2,4-dione
EP0184752A2 (de)	1986-06-18	Neue 2,4-Diaminopyrimidine
EP0300313A2 (de)	1989-01-25	Substituierte Triazine
DE3201110A1 (de)	1983-07-28	3-alken(in)yl-mercapto(amino)-4-amino-6-tert.-butyl-1,2,4-triazin-5-one, verfahren zu ihrer herstellung sowie ihrer verwendung als herbizide
DE3135392A1 (de)	1983-03-17	"substituierte 6-alkoxy-tert.-butyl-1,2,4-triazin-5-one, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide"
DE2937645A1 (de)	1981-04-16	Tetrahydropyranether-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide
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DD207846A5 (de)	1984-03-21	Herbizide mittel
DE3433541A1 (de)	1986-03-20	Herbizide mittel enthaltend photosynthesehemmer-herbizide in kombination mit carbamat-derivaten
EP0094538A2 (de)	1983-11-23	Fluorhaltige 4,6-Diamino-s-triazine, Verfahren und neue Zwischenprodukte zu ihrer Herstellung und ihre Verwendung als Herbizide
DE3431916A1 (de)	1986-03-13	Fluoralkoxyphenylsulfonylguanidine
DE3335477A1 (de)	1985-04-18	2-aryl-2-halogenalkyl-oxirane
DD237784A5 (de)	1986-07-30	Herbizide mittel
DE4239296A1 (de)	1994-05-26	Substituierte Triazolinone
DE3135413A1 (de)	1983-03-24	"azomethine von 4-amino-6-halogen-tert.-butyl-1,2,4 -triazin-5-onen, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide"
DE2842280A1 (de)	1980-04-10	N-(1,3-azolyl)-alkyl-halogenacetanilide, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide
DE3601800A1 (de)	1987-07-23	Neue 2,4-diamino-6-halogenalkylpyrimidine
DE3417264A1 (de)	1985-11-14	Neue 2,4-diamino-6-halogen-5-alkylthio-pyrimidine
DE3220524A1 (de)	1983-12-01	4,4'-disubstituierte diphenylether, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE3306197A1 (de)	1984-08-23	Alkoximinoalkylamino-1,3,5-triazine, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE3323934A1 (de)	1985-01-03	3,6-disubstituierte 4-amino-1,2,4-triazin-5-one
DE3525978A1 (de)	1987-01-29	Azolyl-alkene und -alkine