DD283321A5 - Herbizid wirksame zusammensetzungen - Google Patents

Herbizid wirksame zusammensetzungen Download PDF

Info

Publication number: DD283321A5
Authority: DD; German Democratic Republic
Prior art keywords: phenoxy; quinoxalinyloxy; chloro; propionic acid; ester
Prior art date: 1988-01-06

Application number

DD89324857A

Other languages

German (de)

English (en)

Inventor

Robert Glenn Davis

Allyn Roy Bell

John Adrian Minatelli

Original Assignee

��@��@��@��Kk��

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.)

1988-01-06

Filing date

1989-01-05

Publication date

1990-10-10

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22494538&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DD283321(A5) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1989-01-05 Application filed by ��@��@��@��Kk�� filed Critical ��@��@��@��Kk��

1990-10-10 Publication of DD283321A5 publication Critical patent/DD283321A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 23
230000002363 herbicidal effect Effects 0.000 title claims description 5
239000004009 herbicide Substances 0.000 title abstract description 19
150000001875 compounds Chemical class 0.000 claims abstract description 43
-1 alkylene heterocyclic ester derivatives of quinoxalinyloxyphenoxypropionic acid Chemical class 0.000 claims abstract description 36
238000000034 method Methods 0.000 claims abstract description 16
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 15
229910052739 hydrogen Inorganic materials 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
125000004043 oxo group Chemical group O=* 0.000 claims description 7
229920006395 saturated elastomer Polymers 0.000 claims description 6
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
125000006371 dihalo methyl group Chemical group 0.000 claims description 5
150000002431 hydrogen Chemical class 0.000 claims description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
125000004430 oxygen atom Chemical group O* 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
125000004953 trihalomethyl group Chemical group 0.000 claims description 5
230000012010 growth Effects 0.000 claims description 4
125000006372 monohalo methyl group Chemical group 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
125000005879 dioxolanyl group Chemical group 0.000 claims description 3
125000002541 furyl group Chemical group 0.000 claims description 3
235000019260 propionic acid Nutrition 0.000 claims description 3
125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 claims description 3
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 3
125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims description 2
125000004494 ethyl ester group Chemical group 0.000 claims 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
241000196324 Embryophyta Species 0.000 abstract description 19
241000209504 Poaceae Species 0.000 abstract description 3
230000008635 plant growth Effects 0.000 abstract description 3
239000003795 chemical substances by application Substances 0.000 abstract description 2
239000002689 soil Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
FCMCRFMYSONEAN-UHFFFAOYSA-N 2-phenoxy-2-quinoxalin-2-yloxypropanoic acid Chemical class C=1N=C2C=CC=CC2=NC=1OC(C(O)=O)(C)OC1=CC=CC=C1 FCMCRFMYSONEAN-UHFFFAOYSA-N 0.000 description 6
125000000623 heterocyclic group Chemical group 0.000 description 6
ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 description 5
244000025254 Cannabis sativa Species 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-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
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
244000062793 Sorghum vulgare Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000012153 distilled water Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 description 2
240000006995 Abutilon theophrasti Species 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000008187 granular material Substances 0.000 description 2
150000007529 inorganic bases Chemical class 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
235000019713 millet Nutrition 0.000 description 2
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
150000007530 organic bases Chemical class 0.000 description 2
239000005416 organic matter Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
YCQGFDCYYFHYEP-UHFFFAOYSA-N oxolan-2-ylmethyl 2-bromopropanoate Chemical compound CC(Br)C(=O)OCC1CCCO1 YCQGFDCYYFHYEP-UHFFFAOYSA-N 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
229910000027 potassium carbonate Inorganic materials 0.000 description 2
125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 2
239000004576 sand Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
241000894007 species Species 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 1
SXERGJJQSKIUIC-UHFFFAOYSA-N 2-Phenoxypropionic acid Chemical class OC(=O)C(C)OC1=CC=CC=C1 SXERGJJQSKIUIC-UHFFFAOYSA-N 0.000 description 1
OZGMODDEIHYPRY-UHFFFAOYSA-N 2-bromopropanoyl chloride Chemical compound CC(Br)C(Cl)=O OZGMODDEIHYPRY-UHFFFAOYSA-N 0.000 description 1
CGUXGNBXUPVTPJ-UHFFFAOYSA-N 2-quinoxalin-2-yloxyphenol Chemical compound OC1=CC=CC=C1OC1=CN=C(C=CC=C2)C2=N1 CGUXGNBXUPVTPJ-UHFFFAOYSA-N 0.000 description 1
IWVXWAQUTVWUIC-UHFFFAOYSA-N 2-quinoxalin-2-ylphenol Chemical class OC1=C(C=CC=C1)C1=NC2=CC=CC=C2N=C1 IWVXWAQUTVWUIC-UHFFFAOYSA-N 0.000 description 1
125000006224 2-tetrahydrofuranylmethyl group Chemical group [H]C([H])(*)C1([H])OC([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
ALRHLSYJTWAHJZ-UHFFFAOYSA-N 3-hydroxypropionic acid Chemical compound OCCC(O)=O ALRHLSYJTWAHJZ-UHFFFAOYSA-N 0.000 description 1
UVYFSLAJRJHGJB-UHFFFAOYSA-N 4-(6-chloroquinoxalin-2-yl)oxyphenol Chemical compound C1=CC(O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 UVYFSLAJRJHGJB-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
244000105624 Arachis hypogaea Species 0.000 description 1
VHOMAPWVLKRQAZ-UHFFFAOYSA-N Benzyl propionate Chemical class CCC(=O)OCC1=CC=CC=C1 VHOMAPWVLKRQAZ-UHFFFAOYSA-N 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000208296 Datura Species 0.000 description 1
240000008853 Datura stramonium Species 0.000 description 1
244000058871 Echinochloa crus-galli Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
206010020751 Hypersensitivity Diseases 0.000 description 1
240000001549 Ipomoea eriocarpa Species 0.000 description 1
235000005146 Ipomoea eriocarpa Nutrition 0.000 description 1
235000003403 Limnocharis flava Nutrition 0.000 description 1
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
241001520808 Panicum virgatum Species 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
230000007815 allergy Effects 0.000 description 1
150000004808 allyl alcohols 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
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
238000009835 boiling Methods 0.000 description 1
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000006264 debenzylation reaction Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
230000035558 fertility Effects 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
XXROGKLTLUQVRX-UHFFFAOYSA-N hydroxymethylethylene Natural products OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 1
229940060367 inert ingredients Drugs 0.000 description 1
230000007794 irritation Effects 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
WCRGPZOHLISAKX-UHFFFAOYSA-N oxiran-2-ylmethyl 2-phenoxy-2-quinoxalin-2-yloxypropanoate Chemical class C=1N=C2C=CC=CC2=NC=1OC(C(=O)OCC1OC1)(C)OC1=CC=CC=C1 WCRGPZOHLISAKX-UHFFFAOYSA-N 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
239000008188 pellet 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
BOTNYLSAWDQNEX-UHFFFAOYSA-N phenoxymethylbenzene Chemical compound C=1C=CC=CC=1COC1=CC=CC=C1 BOTNYLSAWDQNEX-UHFFFAOYSA-N 0.000 description 1
230000004962 physiological condition Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
150000003252 quinoxalines Chemical class 0.000 description 1
BBKDWPHJZANJGB-UHFFFAOYSA-N quizalofop-p-tefuryl Chemical compound C=1C=C(OC=2N=C3C=CC(Cl)=CC3=NC=2)C=CC=1OC(C)C(=O)OCC1CCCO1 BBKDWPHJZANJGB-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
229910052604 silicate mineral Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000021 stimulant Substances 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
125000005490 tosylate group Chemical group 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (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)

DD89324857A 1988-01-06 1989-01-05 Herbizid wirksame zusammensetzungen DD283321A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US14118288A	1988-01-06	1988-01-06

Publications (1)

Publication Number	Publication Date
DD283321A5 true DD283321A5 (de)	1990-10-10

Family

ID=22494538

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD89324857A DD283321A5 (de)	1988-01-06	1989-01-05	Herbizid wirksame zusammensetzungen

Country Status (24)

Country	Link
EP (1)	EP0323727B1 (es)
JP (1)	JPH0725753B2 (es)
KR (1)	KR0120267B1 (es)
CN (1)	CN1022369C (es)
AR (1)	AR248277A1 (es)
AT (1)	ATE93857T1 (es)
AU (2)	AU615503B2 (es)
BR (1)	BR8900004A (es)
CA (1)	CA1340481C (es)
CZ (1)	CZ278965B6 (es)
DD (1)	DD283321A5 (es)
DE (2)	DE3883739T2 (es)
EG (1)	EG19502A (es)
ES (1)	ES2058314T3 (es)
FI (1)	FI91153C (es)
HU (1)	HU201545B (es)
IL (1)	IL88754A (es)
MY (1)	MY104385A (es)
PL (1)	PL153976B1 (es)
PT (1)	PT89394B (es)
RU (2)	RU1837770C (es)
SK (1)	SK278176B6 (es)
TR (1)	TR24425A (es)
ZA (1)	ZA889732B (es)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR8801855A (pt) *	1987-04-20	1988-11-22	Agro Kanesho Co Ltd	Composicao herbicida compreendendo como ingrediente ativo um derivado de ester de acido fenoxipropionico e processo para a producao de derivados de ester de acido fenoxipropionico
US5319102A (en) *	1988-01-06	1994-06-07	Uniroyal Chemical Company, Inc.	Heterocyclic-alkylene quinoxalinyloxyphenoxypropanoate herbicides
US5120348A (en) *	1988-01-06	1992-06-09	Uniroyal Chemical Company, Inc.	Heterocyclic-alkylene quinoxalinyloxyphenoxypropanoate herbicides
US5258521A (en) *	1989-07-26	1993-11-02	Tosoh Corporation	Process of producing optically active propionic acid ester derivatives
DE4042098C2 (de) *	1990-12-28	1993-10-07	Hoechst Ag	Verfahren zur Herstellung optisch aktiver Chinoxalinyloxy-phenoxypropionsäureester
AU5686794A (en) *	1992-12-15	1994-07-04	Du Pont Merck Pharmaceutical Company, The	(2-quinoxalinyloxy)phenoxypropanoic acids and related derivatives as anticancer agents
CA2257204C (en) *	1996-06-03	2006-07-11	Nissan Chemical Industries, Ltd.	Processes for producing phenoxy propionic acid derivatives
EP1836894A1 (de)	2006-03-25	2007-09-26	Bayer CropScience GmbH	Neue Sulfonamid-haltige feste Formulungen
EP1844654A1 (de)	2006-03-29	2007-10-17	Bayer CropScience GmbH	Penetrationsförderer für agrochemische Wirkstoffe
DE102007013362A1 (de)	2007-03-16	2008-09-18	Bayer Cropscience Ag	Penetrationsförderer für herbizide Wirkstoffe
WO2011076731A1 (de)	2009-12-23	2011-06-30	Bayer Cropscience Ag	Flüssige formulierung von 2-iodo-n-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl] benzolsulfonamid
WO2012110517A1 (en)	2011-02-15	2012-08-23	Bayer Cropscience Ag	Synergistic combinations containing a dithiino-tetracarboxamide fungicide and a herbicide, safener or plant growth regulator
DE102011080007A1 (de)	2011-07-28	2012-09-13	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Conazole- und Triazol-Fungizide als Safener
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DE102011080016A1 (de)	2011-07-28	2012-10-25	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Strobilurin-Fungizide als Safener
DE102011080020A1 (de)	2011-07-28	2012-09-13	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Dicarboximid-Fungizide als Safener
DE102011080001A1 (de)	2011-07-28	2012-10-25	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Carbamat-Insektizide als Safener
DE102011080010A1 (de)	2011-07-28	2012-10-25	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Anilid- und Thiazol-Fungizide als Safener
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1988
- 1988-12-20 EP EP88312047A patent/EP0323727B1/en not_active Expired - Lifetime
- 1988-12-20 AT AT88312047T patent/ATE93857T1/de not_active IP Right Cessation
- 1988-12-20 DE DE88312047T patent/DE3883739T2/de not_active Expired - Lifetime
- 1988-12-20 DE DE122008000064C patent/DE122008000064I2/de active Active
- 1988-12-20 ES ES88312047T patent/ES2058314T3/es not_active Expired - Lifetime
- 1988-12-21 IL IL88754A patent/IL88754A/xx unknown
- 1988-12-21 AU AU27449/88A patent/AU615503B2/en not_active Expired
- 1988-12-29 KR KR1019880017741A patent/KR0120267B1/ko not_active Expired - Lifetime
- 1988-12-29 ZA ZA889732A patent/ZA889732B/xx unknown
- 1988-12-29 EG EG66488A patent/EG19502A/xx active
1989
- 1989-01-02 BR BR898900004A patent/BR8900004A/pt not_active IP Right Cessation
- 1989-01-03 MY MYPI89000003A patent/MY104385A/en unknown
- 1989-01-03 TR TR89/0029A patent/TR24425A/xx unknown
- 1989-01-04 AR AR89312921A patent/AR248277A1/es active
- 1989-01-05 DD DD89324857A patent/DD283321A5/de unknown
- 1989-01-05 HU HU8932A patent/HU201545B/hu unknown
- 1989-01-05 JP JP64000814A patent/JPH0725753B2/ja not_active Expired - Lifetime
- 1989-01-05 CN CN89100091A patent/CN1022369C/zh not_active Expired - Lifetime
- 1989-01-05 PT PT89394A patent/PT89394B/pt not_active IP Right Cessation
- 1989-01-05 RU SU894613266A patent/RU1837770C/ru active
- 1989-01-05 RU RU92004428A patent/RU2111210C1/ru active
- 1989-01-05 PL PL1989277055A patent/PL153976B1/pl unknown
- 1989-01-05 CZ CS8994A patent/CZ278965B6/cs unknown
- 1989-01-05 SK SK94-89A patent/SK278176B6/sk unknown
- 1989-01-05 FI FI890060A patent/FI91153C/fi not_active IP Right Cessation
- 1989-01-06 CA CA000587018A patent/CA1340481C/en not_active Expired - Lifetime
1991
- 1991-07-24 AU AU81301/91A patent/AU620760B2/en not_active Expired

Also Published As

Publication number	Publication date
AU2744988A (en)	1989-07-06
KR0120267B1 (ko)	1997-11-04
HUT49877A (en)	1989-11-28
ATE93857T1 (de)	1993-09-15
FI91153C (fi)	1994-05-25
EP0323727B1 (en)	1993-09-01
BR8900004A (pt)	1989-08-15
CZ9489A3 (en)	1994-06-15
FI890060L (fi)	1989-07-07
CZ278965B6 (en)	1994-11-16
FI91153B (fi)	1994-02-15
EG19502A (en)	1995-06-29
RU2111210C1 (ru)	1998-05-20
DE122008000064I2 (de)	2011-06-16
DE3883739D1 (de)	1993-10-07
AR248277A1 (es)	1995-07-12
RU1837770C (ru)	1993-08-30
IL88754A (en)	1993-04-04
CN1035505A (zh)	1989-09-13
PT89394B (pt)	1993-09-30
PL277055A1 (en)	1990-01-08
IL88754A0 (en)	1989-07-31
AU615503B2 (en)	1991-10-03
HU201545B (en)	1990-11-28
DE3883739T2 (de)	1994-01-20
AU620760B2 (en)	1992-02-20
TR24425A (tr)	1991-10-08
ES2058314T3 (es)	1994-11-01
EP0323727A3 (en)	1990-08-08
KR890011877A (ko)	1989-08-23
PT89394A (pt)	1990-02-08
PL153976B1 (en)	1991-06-28
AU8130191A (en)	1991-10-10
JPH01246278A (ja)	1989-10-02
EP0323727A2 (en)	1989-07-12
SK9489A3 (en)	1996-03-06
MY104385A (en)	1994-03-31
JPH0725753B2 (ja)	1995-03-22
CA1340481C (en)	1999-04-06
ZA889732B (en)	1989-10-25
SK278176B6 (en)	1996-03-06
CN1022369C (zh)	1993-10-13
FI890060A0 (fi)	1989-01-05

Legal Events

Date	Code	Title	Description
2004-04-28	IF04	In force in the year 2004	Expiry date: 20090106

Publication	Publication Date	Title
DD283321A5 (de)	1990-10-10	Herbizid wirksame zusammensetzungen
EP0003313B1 (de)	1981-01-07	Neue Pyridyloxy-phenoxy-alpha-propionsäure-aminoalkyl-ester mit herbizider Wirkung,ihre Herstellung, sie enthaltende Mittel und deren Verwendung
CH656612A5 (de)	1986-07-15	Herbizide 3-isoxazolidinone und hydroxamsaeuren.
CH644371A5 (de)	1984-07-31	In 2- und 4-stellung disubstituierte 5-thiazolcarbonsaeuren und deren funktionelle derivate.
DD259993A5 (de)	1988-09-14	Herbizide mittel
EP0332009A1 (de)	1989-09-13	N-Aryltetrahydrophthalimidverbindungen
EP0036390A2 (de)	1981-09-23	Diphenyläther-Harnstoffe mit herbizider Wirkung
EP0007089B1 (de)	1981-09-16	Acylanilide mit herbicider und fungicider Wirkung, Verfahren zu ihrer Herstellung und ihre Verwendung
EP0305332A2 (de)	1989-03-01	Imidazol-Derivate
DD210190A5 (de)	1984-06-06	Herbizides mittel
EP0058639A2 (de)	1982-08-25	2-(4-(6-Halogen-chinoxalinyl-2-oxy)-phenoxy)-propionsäureester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Herbizide und Pflanzenwuchsregulatoren
AT397246B (de)	1994-02-25	Neue ester und sie enthaltendes herbizides mittel
DD262992A5 (de)	1988-12-21	Nematizide und insektizide zusammensetzung
EP0034120B1 (de)	1983-12-14	Neue Phenoxy-phenoxy-carbonsäurederivate
EP0013542B1 (de)	1982-06-02	Alpha-Phenoxy-propionsäure-gamma-butyrolactonester und -thioester mit herbizider Wirkung, deren Herstellung,sie als Wirkstoffe enthaltende Mittel und deren Verwendung
DD236868A5 (de)	1986-06-25	Mittel zum protahieren der wirkungsdauer und zur erhoehung der selektivitaet von herbiziden zusammensetzungen
EP0027915B1 (de)	1983-05-18	Herbizide Mittel auf der Basis von Diphenyläthern und Benzothiadiazinondioxiden bzw. Pyridinothiadiazinondioxiden und deren Verwendung
DE1567217C3 (de)	1975-05-15	Tetrachlorterephthalsäurederivate, Verfahren zu deren Herstellung und ihre Verwendung als Herbicide
DE3136913A1 (de)	1983-04-21	"herbizide mittel"
CH645375A5 (de)	1984-09-28	Alpha-(4-(5'-trifluormethylpyridyl-2'-oxy)-phenoxy)-propionsaeure-gamma-butyrolacton-ester und -thioester mit herbizider wirkung, ihre herstellung und verwendung.
EP0148445A2 (de)	1985-07-17	Herbizide Mittel auf Basis von Dichlorchinolinderivaten
CH645353A5 (de)	1984-09-28	Carbostyrilderivate.
DE2111156A1 (de)	1972-09-14	Insektizide Mittel
EP0347378A1 (de)	1989-12-20	Imidazol-Derivate
DE2004020B2 (de)	1973-11-08	Cyclopropancarbonsaureester Verfahren zu ihrer Herstellung und ihre Verwendung