DD153565A5 - Herbizide mittel - Google Patents

Herbizide mittel Download PDF

Info

Publication number: DD153565A5
Authority: DD; German Democratic Republic
Prior art keywords: parts; radical; carbon atoms; substituted; aliphatic radical
Prior art date: 1979-10-30

Application number

DD22478080A

Other languages

German (de)

English (en)

Inventor

Gerhard Hamprecht

Rolf-Dieter Acker

Bruno Wuerzer

Original Assignee

Basf 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.)

1979-10-30

Filing date

1980-10-28

Publication date

1982-01-20

1980-10-28 Application filed by Basf Ag filed Critical Basf Ag

1982-01-20 Publication of DD153565A5 publication Critical patent/DD153565A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims description 11
239000004009 herbicide Substances 0.000 title abstract description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 3
229910052736 halogen Inorganic materials 0.000 claims abstract description 3
150000002367 halogens Chemical class 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
150000002431 hydrogen Chemical group 0.000 claims abstract description 3
239000001301 oxygen Substances 0.000 claims abstract description 3
229910052760 oxygen Inorganic materials 0.000 claims abstract description 3
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims abstract description 3
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims abstract description 3
229910052717 sulfur Inorganic materials 0.000 claims abstract description 3
239000011593 sulfur Chemical group 0.000 claims abstract description 3
-1 aliphatic radical Chemical class 0.000 claims description 52
239000000203 mixture Substances 0.000 claims description 29
125000004432 carbon atom Chemical group C* 0.000 claims description 18
150000003254 radicals Chemical class 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical class [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 2
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125000000217 alkyl group Chemical group 0.000 claims description 2
239000007788 liquid Substances 0.000 claims 1
239000007787 solid Substances 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract description 15
238000002360 preparation method Methods 0.000 abstract description 8
238000000034 method Methods 0.000 abstract description 5
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 2
XRZMJWVYXJGIKB-UHFFFAOYSA-N 4h-1,2,4,6-thiatriazine 1,1-dioxide Chemical class O=S1(=O)NC=NC=N1 XRZMJWVYXJGIKB-UHFFFAOYSA-N 0.000 abstract 1
125000000547 substituted alkyl group Chemical group 0.000 abstract 1
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QZOFFMRDIRXGKJ-UHFFFAOYSA-M hydron;4-pyridin-1-ium-1-ylpyridine;dichloride Chemical compound Cl.[Cl-].C1=CC=CC=[N+]1C1=CC=NC=C1 QZOFFMRDIRXGKJ-UHFFFAOYSA-M 0.000 description 1
239000005457 ice water Substances 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine 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
LRDFRRGEGBBSRN-UHFFFAOYSA-N isobutyronitrile Chemical compound CC(C)C#N LRDFRRGEGBBSRN-UHFFFAOYSA-N 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
125000005394 methallyl group Chemical group 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
VPXUUNZJNXQNNN-UHFFFAOYSA-N methyl (ne)-n-[amino(benzylsulfanyl)methylidene]carbamate Chemical compound COC(=O)NC(=N)SCC1=CC=CC=C1 VPXUUNZJNXQNNN-UHFFFAOYSA-N 0.000 description 1
DEZNOFAJXWNMHJ-UHFFFAOYSA-N methyl (ne)-n-[amino(methoxy)methylidene]carbamate Chemical compound COC(N)=NC(=O)OC DEZNOFAJXWNMHJ-UHFFFAOYSA-N 0.000 description 1
ZTZUHYBWXYVNLO-UHFFFAOYSA-N methyl N-methyl-N-(methylsulfamoyloxycarbamoyl)carbamate Chemical compound C(=O)(OC)N(C(=O)NOS(NC)(=O)=O)C ZTZUHYBWXYVNLO-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 1
PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
DLMICMXXVVMDNV-UHFFFAOYSA-N n,n-di(propan-2-yl)propan-1-amine Chemical compound CCCN(C(C)C)C(C)C DLMICMXXVVMDNV-UHFFFAOYSA-N 0.000 description 1
FGZSEUXOFDMNEL-UHFFFAOYSA-N n-cyclohexylsulfamoyl chloride Chemical compound ClS(=O)(=O)NC1CCCCC1 FGZSEUXOFDMNEL-UHFFFAOYSA-N 0.000 description 1
JIKUXBYRTXDNIY-UHFFFAOYSA-N n-methyl-n-phenylformamide Chemical compound O=CN(C)C1=CC=CC=C1 JIKUXBYRTXDNIY-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
239000006072 paste Substances 0.000 description 1
BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
235000011197 perejil Nutrition 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
229930006728 pinane Natural products 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
235000014774 prunus Nutrition 0.000 description 1
JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
QHMQWEPBXSHHLH-UHFFFAOYSA-N sulfur tetrafluoride Chemical compound FS(F)(F)F QHMQWEPBXSHHLH-UHFFFAOYSA-N 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
- C07C311/52—Y being a hetero atom
- C07C311/54—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea
- C07C311/63—N-sulfonylisoureas

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)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Treating Waste Gases (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

DD22478080A 1979-10-30 1980-10-28 Herbizide mittel DD153565A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19792943703 DE2943703A1 (de)	1979-10-30	1979-10-30	6h-1,2,4,6-thiatriazin-1,1-dioxide, herbizide, die diese verbindungen enthalten, ihre anwendung als herbizide und verfahren zu ihrer herstellung

Publications (1)

Publication Number	Publication Date
DD153565A5 true DD153565A5 (de)	1982-01-20

Family

ID=6084671

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD22478080A DD153565A5 (de)	1979-10-30	1980-10-28	Herbizide mittel

Country Status (15)

Country	Link
US (1)	US4316015A (da)
EP (1)	EP0029908B1 (da)
JP (1)	JPS5679684A (da)
AT (1)	ATE2044T1 (da)
AU (1)	AU534773B2 (da)
BR (1)	BR8006920A (da)
CA (1)	CA1139753A (da)
DD (1)	DD153565A5 (da)
DE (2)	DE2943703A1 (da)
DK (1)	DK458280A (da)
ES (1)	ES8200100A1 (da)
HU (1)	HU185912B (da)
IL (1)	IL61275A (da)
SU (1)	SU936792A3 (da)
ZA (1)	ZA8006613D (da)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3134143A1 (de) *	1981-08-28	1983-03-17	Basf Ag, 6700 Ludwigshafen	2h-1,2,4,6-thiatriazin-1,1-dioxide, ein verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
DE3143381A1 (de) *	1981-11-02	1983-05-11	Basf Ag, 6700 Ludwigshafen	1,2,4,6-thiatriazin-1,1,-dioxide, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenchenten pflanzenwuchses
US4497810A (en) *	1983-10-14	1985-02-05	Merck & Co., Inc.	Thiatriazine dioxides as gastric anti-secretory agents
US4704388A (en) *	1984-10-23	1987-11-03	Rorer Pharmaceutical Corporation	3- And 5-(bicyclic ether or bicyclic alkylene thioether)alkylene amino thiatriazines, and their pharmaceutical uses
US4595683A (en) *	1984-04-27	1986-06-17	William H. Rorer, Inc.	3- and 5-[bicyclic ether or bicyclic alkylene thioether]alkylene amino thiatriazines, and their pharmaceutical uses
US4742055A (en) *	1984-04-27	1988-05-03	Rorer Pharmaceutical Corporation	3- and 5-amino thiatriazines, and their pharmaceutical uses
AU1303897A (en) *	1996-01-05	1997-08-01	Ciba-Geigy Ag	Herbicidal 1,2,4,6-thiatriazines
US6335339B1 (en)	1998-01-13	2002-01-01	Scriptgen Pharmaceuticals, Inc.	Triazine antiviral compounds

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1946262A1 (de) *	1969-09-12	1971-03-18	Bayer Ag	Derivate des 2,3-Dihydro-4H-1,2,4,6-thiatriazin-3-on-1-dioxids
DE2026625A1 (en) *	1970-05-30	1971-12-16	Farbenfabriken Bayer AG, 5090 Le verkusen	Thiatriazine cpds - useful as plant protection agents
US4013447A (en) *	1974-03-01	1977-03-22	Imperial Chemical Industries Limited	Compositions containing herbicidal thiatriazinone derivatives and use thereof

1979
- 1979-10-30 DE DE19792943703 patent/DE2943703A1/de not_active Withdrawn
1980
- 1980-10-15 IL IL61275A patent/IL61275A/xx unknown
- 1980-10-20 CA CA000362773A patent/CA1139753A/en not_active Expired
- 1980-10-21 EP EP80106394A patent/EP0029908B1/de not_active Expired
- 1980-10-21 AT AT80106394T patent/ATE2044T1/de not_active IP Right Cessation
- 1980-10-21 DE DE8080106394T patent/DE3061443D1/de not_active Expired
- 1980-10-23 SU SU802995661A patent/SU936792A3/ru active
- 1980-10-23 US US06/199,820 patent/US4316015A/en not_active Expired - Lifetime
- 1980-10-28 HU HU802600A patent/HU185912B/hu not_active IP Right Cessation
- 1980-10-28 DD DD22478080A patent/DD153565A5/de unknown
- 1980-10-29 BR BR8006920A patent/BR8006920A/pt unknown
- 1980-10-29 DK DK458280A patent/DK458280A/da not_active Application Discontinuation
- 1980-10-29 JP JP15085180A patent/JPS5679684A/ja active Pending
- 1980-10-29 ES ES496388A patent/ES8200100A1/es not_active Expired
- 1980-10-29 ZA ZA19806613D patent/ZA8006613D/xx unknown
- 1980-10-29 AU AU63804/80A patent/AU534773B2/en not_active Ceased

Also Published As

Publication number	Publication date
ES496388A0 (es)	1981-10-16
ES8200100A1 (es)	1981-10-16
CA1139753A (en)	1983-01-18
DE2943703A1 (de)	1981-05-27
EP0029908A1 (de)	1981-06-10
IL61275A (en)	1984-03-30
EP0029908B1 (de)	1982-12-22
ZA8006613D (en)	1981-11-25
ATE2044T1 (de)	1983-01-15
DE3061443D1 (en)	1983-01-27
IL61275A0 (en)	1980-12-31
US4316015A (en)	1982-02-16
SU936792A3 (ru)	1982-06-15
HU185912B (en)	1985-04-28
DK458280A (da)	1981-05-01
AU534773B2 (en)	1984-02-16
JPS5679684A (en)	1981-06-30
BR8006920A (pt)	1981-05-05
AU6380480A (en)	1981-05-07

Publication	Publication Date	Title
EP0559814B1 (de)	1998-09-09	Herbizide n- (1,3,5-triazin-2-yl)aminocarbonyl]benzolsulfonamide
DE3305866A1 (de)	1984-08-23	Thiophen-carbonester, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
EP0482349B1 (de)	2001-07-04	Sulfonamide mit herbiziden Eigenschaften.
EP0628031B1 (de)	1999-06-16	Herbizide n- (pyrimidin-2-yl)aminocarbonyl]benzolsulfonamide
DD153565A5 (de)	1982-01-20	Herbizide mittel
DD292917A5 (de)	1991-08-14	Herbizide [[(1,3,5-triazin-2-yl) aminocarbonyl] aminosulfonyl] benzoesaeureester, verfahren zu ihrer herstellung und ihre verwendung
WO1994011358A1 (de)	1994-05-26	Herbizide sulfonylharnstoffe, verfahren zur herstellung und ihre verwendung
DE3716657A1 (de)	1988-12-01	Herbizide sulfonamide, verfahren zu ihrer herstellung und ihre verwendung zur beeinflussung des pflanzenwachstums
DD158734A5 (de)	1983-02-02	Herbizide mittel
EP0075117A2 (de)	1983-03-30	2H-1,2,4,6-Thiatriazin-1,1-dioxide, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
EP0025113B1 (de)	1983-07-20	5.6-Dihydro-1.2.4.6-thiatriazin(5)on-1.1-dioxide, Verfahren zu ihrer Herstellung und diese enthaltende Herbizide
WO1993005048A2 (de)	1993-03-18	Herbizide sulfonylharnstoffe, verfahren und zwischenprodukte zu ihrer herstellung
EP0073443B1 (de)	1986-11-05	2H-1,2,4,6-Thiatriazin-1,1-dioxide, ein Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE3900472A1 (de)	1990-07-12	Herbizide sulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung
DE3222974A1 (de)	1983-12-22	Neue 5-phenoxybenzisothiazol-4'-harnstoffderivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE3813623A1 (de)	1989-11-02	N-((6-trifluormethylpyrimidin-2-yl)- aminocarbonyl)-2-carboalkoxybenzolsulfonamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder zur beeinflussung des pflanzenwachstums
DE4024754A1 (de)	1992-02-06	Herbizide sulfonylharnstoffe, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung
DE3308239A1 (de)	1984-09-13	N-acyl-anthranilsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
EP0116167B1 (de)	1986-02-26	Diphenylether, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
EP0102542B1 (de)	1990-07-04	1,2,4,6-Thiatriazin-1,1-dioxid-ether, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE3429437A1 (de)	1985-06-20	Cyclohexenonderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
DE3418532A1 (de)	1985-06-13	Chinolinoxyphenylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
EP0078462A1 (de)	1983-05-11	1,2,4,6-Thiatriazin-1,1-dioxide, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
EP0191394B1 (de)	1989-12-06	Isothioharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DD201749A5 (de)	1983-08-10	Herbizide mittel