DD203222A5 - Mittel zur bekaempfung von unkraeutern - Google Patents

Mittel zur bekaempfung von unkraeutern Download PDF

Info

Publication number: DD203222A5
Authority: DD; German Democratic Republic
Prior art keywords: hydrogen; alkyl; substituted; compounds; item
Prior art date: 1981-08-07

Application number

DD82242278A

Other languages

German (de)

English (en)

Inventor

Dieter Duerr

Original Assignee

Ciba Geigy

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.)

1981-08-07

Filing date

1982-08-05

Publication date

1983-10-19

1982-08-05 Application filed by Ciba Geigy filed Critical Ciba Geigy

1983-10-19 Publication of DD203222A5 publication Critical patent/DD203222A5/de

Links

239000001257 hydrogen Substances 0.000 claims abstract description 188
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 188
-1 Phenoxyphenyl-amino Chemical group 0.000 claims abstract description 126
150000001875 compounds Chemical class 0.000 claims abstract description 110
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 71
125000000217 alkyl group Chemical group 0.000 claims abstract description 49
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 46
125000001424 substituent group Chemical group 0.000 claims abstract description 46
239000000460 chlorine Chemical group 0.000 claims abstract description 37
229910052801 chlorine Inorganic materials 0.000 claims abstract description 28
239000000203 mixture Substances 0.000 claims abstract description 28
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 26
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 20
150000001768 cations Chemical class 0.000 claims abstract description 17
125000003545 alkoxy group Chemical group 0.000 claims abstract description 16
125000000304 alkynyl group Chemical group 0.000 claims abstract description 10
230000035613 defoliation Effects 0.000 claims abstract description 10
229910052736 halogen Inorganic materials 0.000 claims abstract description 10
150000002367 halogens Chemical group 0.000 claims abstract description 10
150000002431 hydrogen Chemical group 0.000 claims abstract description 9
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 8
239000011737 fluorine Chemical group 0.000 claims abstract description 8
229910052731 fluorine Inorganic materials 0.000 claims abstract description 8
238000002360 preparation method Methods 0.000 claims abstract description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 7
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 7
229910052794 bromium Chemical group 0.000 claims abstract description 7
125000005090 alkenylcarbonyl group Chemical group 0.000 claims abstract description 6
244000061456 Solanum tuberosum Species 0.000 claims abstract description 5
125000005843 halogen group Chemical group 0.000 claims abstract description 5
229920000742 Cotton Polymers 0.000 claims abstract description 4
125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract description 3
230000008635 plant growth Effects 0.000 claims abstract 2
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 109
241000196324 Embryophyta Species 0.000 claims description 30
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 29
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 14
125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 12
239000003795 chemical substances by application Substances 0.000 claims description 12
125000003342 alkenyl group Chemical group 0.000 claims description 10
239000004094 surface-active agent Substances 0.000 claims description 10
239000002253 acid Substances 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 9
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 8
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 8
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
238000000034 method Methods 0.000 claims description 8
125000000018 nitroso group Chemical group N(=O)* 0.000 claims description 8
239000007787 solid Substances 0.000 claims description 8
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 7
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 6
239000007788 liquid Substances 0.000 claims description 6
229910052751 metal Inorganic materials 0.000 claims description 6
239000002184 metal Substances 0.000 claims description 6
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 5
125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims description 4
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 4
240000005979 Hordeum vulgare Species 0.000 claims description 4
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229910052783 alkali metal Inorganic materials 0.000 claims description 4
235000013339 cereals Nutrition 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
125000004672 ethylcarbonyl group Chemical group [H]C([H])([H])C([H])([H])C(*)=O 0.000 claims description 4
239000000463 material Substances 0.000 claims description 4
125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000005977 Ethylene Substances 0.000 claims description 3
230000000996 additive effect Effects 0.000 claims description 3
125000001931 aliphatic group Chemical group 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
125000001153 fluoro group Chemical group F* 0.000 claims description 3
235000019260 propionic acid Nutrition 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
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
239000011230 binding agent Substances 0.000 claims description 2
229910052742 iron Inorganic materials 0.000 claims description 2
239000003921 oil Substances 0.000 claims description 2
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239000003381 stabilizer Substances 0.000 claims description 2
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims 5
125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
150000002500 ions Chemical class 0.000 claims 2
125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims 1
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
241000282979 Alces alces Species 0.000 claims 1
235000002789 Panax ginseng Nutrition 0.000 claims 1
240000004371 Panax ginseng Species 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
235000013305 food Nutrition 0.000 claims 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
238000005554 pickling Methods 0.000 claims 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
101100072620 Streptomyces griseus ind2 gene Proteins 0.000 abstract 4
101100242909 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) pbpA gene Proteins 0.000 abstract 3
101100269618 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) aliA gene Proteins 0.000 abstract 3
101100439974 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) clpE gene Proteins 0.000 abstract 3
101100354192 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) exp5 gene Proteins 0.000 abstract 3
101100502015 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) exp7 gene Proteins 0.000 abstract 3
101100505001 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) glpO gene Proteins 0.000 abstract 3
101100275845 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) cshA gene Proteins 0.000 abstract 2
101100439746 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) cinA gene Proteins 0.000 abstract 2
101100502016 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) exp8 gene Proteins 0.000 abstract 2
101150109310 msrAB1 gene Proteins 0.000 abstract 2
239000004480 active ingredient Substances 0.000 description 21
239000013543 active substance Substances 0.000 description 11
230000000694 effects Effects 0.000 description 11
230000002363 herbicidal effect Effects 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
150000003839 salts Chemical class 0.000 description 9
239000005995 Aluminium silicate Substances 0.000 description 8
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235000012211 aluminium silicate Nutrition 0.000 description 8
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 8
239000011734 sodium Substances 0.000 description 8
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
239000000839 emulsion Substances 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
240000007594 Oryza sativa Species 0.000 description 6
235000007164 Oryza sativa Nutrition 0.000 description 6
239000002202 Polyethylene glycol Substances 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
240000006694 Stellaria media Species 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
241000209140 Triticum Species 0.000 description 6
235000021307 Triticum Nutrition 0.000 description 6
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MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
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235000014113 dietary fatty acids Nutrition 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
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150000004665 fatty acids Chemical class 0.000 description 5
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QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
241000219144 Abutilon Species 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
235000010469 Glycine max Nutrition 0.000 description 4
244000047670 Viola x wittrockiana Species 0.000 description 4
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238000002474 experimental method Methods 0.000 description 4
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HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
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XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
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JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical group CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 description 1
UIRLNVFJXWEFHI-UHFFFAOYSA-N 2-chloroethyl(ethyl)azanium;bromide Chemical compound [Br-].CC[NH2+]CCCl UIRLNVFJXWEFHI-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical class CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/50—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- 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
- A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- 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
- A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
- 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<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C243/34—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of a carbon skeleton further substituted by nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/50—Y being a hydrogen or an acyclic carbon atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pyrrole Compounds (AREA)

DD82242278A 1981-08-07 1982-08-05 Mittel zur bekaempfung von unkraeutern DD203222A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH509981		1981-08-07
CH350482		1982-06-07

Publications (1)

Publication Number	Publication Date
DD203222A5 true DD203222A5 (de)	1983-10-19

Family

ID=25693191

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD82242278A DD203222A5 (de)	1981-08-07	1982-08-05	Mittel zur bekaempfung von unkraeutern
DD82256212A DD210256A5 (de)	1981-08-07	1982-08-05	Verfahren zur herstellung neuer phenoxyphenylaminosaeure-derivate

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DD82256212A DD210256A5 (de)	1981-08-07	1982-08-05	Verfahren zur herstellung neuer phenoxyphenylaminosaeure-derivate

Country Status (20)

Country	Link
US (1)	US4649212A (cs)
EP (1)	EP0072348B1 (cs)
KR (1)	KR840001130A (cs)
AU (1)	AU8692382A (cs)
BR (1)	BR8204648A (cs)
CS (1)	CS245775B2 (cs)
DD (2)	DD203222A5 (cs)
DE (1)	DE3269621D1 (cs)
DK (1)	DK354282A (cs)
ES (1)	ES8400733A1 (cs)
GB (1)	GB2105715B (cs)
GR (1)	GR77261B (cs)
HU (1)	HU189165B (cs)
IL (1)	IL66472A (cs)
MA (1)	MA19610A1 (cs)
NZ (1)	NZ201519A (cs)
PL (1)	PL141197B1 (cs)
PT (1)	PT75390B (cs)
TR (1)	TR21541A (cs)
ZW (1)	ZW16182A1 (cs)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4913729A (en) *	1981-10-19	1990-04-03	Rohm And Haas Company	Herbicidal 4-trifluoromethyl-3'-substituted amine-4'-nitro diphenyl ethers
DE3265648D1 (en) *	1981-11-09	1985-09-26	Duphar Int Res	New diphenyl ethers having herbicidal activity
EP0126294B1 (en) *	1983-05-06	1986-11-20	Duphar International Research B.V	New diphenyl ethers having herbicidal activity
US5028732A (en) *	1983-06-23	1991-07-02	Rohm And Haas Company	Herbicidally active amino diphenyl ethers
CA1230883A (en) *	1983-06-23	1987-12-29	Ann H. Beaulieu	[2-substituted-5(phenoxy or pyridyloxy]- phenyl-substituted amines
CN110981679B (zh)	2014-09-08	2023-02-17	昭和电工株式会社	卤代化合物和富勒烯衍生物的制造方法

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2169251B1 (cs) *	1972-01-27	1976-05-14	Ishihara Sangyo Kaisha
SE416544B (sv) *	1972-03-14	1981-01-19	Rohm & Haas	Herbicidisk forening samt anvendning som herbicid av foreningen
US3928416A (en) *	1972-03-14	1975-12-23	Rohm & Haas	Herbicidal 4-trifluoromethyl-4{40 nitrodiphenyl ethers
US4069344A (en) *	1972-05-10	1978-01-17	Ciba-Geigy Corporation	Insecticidal substituted phenyl derivatives
FI55986C (fi) *	1972-05-10	1979-11-12	Ciba Geigy Ag	Foer anvaendning som skadedjurs bekaempningsmedel avsedda substituerade fenylderivat
DE2961372D1 (en) *	1978-01-20	1982-01-28	Ciba Geigy Ag	Phenoxy-phenoxy-alkylcarboxylic acid derivatives with herbicidal activity, their preparation, compositions containing them and their use
DE2906237A1 (de) *	1979-02-17	1980-08-28	Bayer Ag	Phenoxycarbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide
EP0021692A1 (en) *	1979-06-11	1981-01-07	Rohm And Haas Company	Novel substituted nitrodiphenyl ethers, herbicidal compositions containing them and the use thereof for combating weeds
DE2938595A1 (de) *	1979-09-24	1981-04-23	Celamerck Gmbh & Co Kg, 6507 Ingelheim	Verfahren zur herstellung von diphenylaethern
DE2950401A1 (de) *	1979-12-14	1981-07-02	Bayer Ag, 5090 Leverkusen	Phenoxybenzoesaeure-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide und pflanzenwuchsregulatoren
JPS5772946A (en) *	1980-10-24	1982-05-07	Mitsui Toatsu Chem Inc	Diphenyl ether compound, its preparation and herbicide

1982
- 1982-08-02 GB GB08222230A patent/GB2105715B/en not_active Expired
- 1982-08-02 MA MA19775A patent/MA19610A1/fr unknown
- 1982-08-02 DE DE8282810324T patent/DE3269621D1/de not_active Expired
- 1982-08-02 EP EP82810324A patent/EP0072348B1/de not_active Expired
- 1982-08-04 TR TR21541A patent/TR21541A/xx unknown
- 1982-08-05 GR GR68968A patent/GR77261B/el unknown
- 1982-08-05 DD DD82242278A patent/DD203222A5/de unknown
- 1982-08-05 ZW ZW161/82A patent/ZW16182A1/xx unknown
- 1982-08-05 DD DD82256212A patent/DD210256A5/de unknown
- 1982-08-05 PL PL1982237790A patent/PL141197B1/pl unknown
- 1982-08-05 IL IL66472A patent/IL66472A/xx unknown
- 1982-08-05 CS CS825844A patent/CS245775B2/cs unknown
- 1982-08-06 AU AU86923/82A patent/AU8692382A/en not_active Abandoned
- 1982-08-06 DK DK354282A patent/DK354282A/da not_active Application Discontinuation
- 1982-08-06 HU HU822536A patent/HU189165B/hu unknown
- 1982-08-06 BR BR8204648A patent/BR8204648A/pt unknown
- 1982-08-06 ES ES514791A patent/ES8400733A1/es not_active Expired
- 1982-08-06 PT PT75390A patent/PT75390B/pt unknown
- 1982-08-06 NZ NZ201519A patent/NZ201519A/en unknown
- 1982-08-07 KR KR1019820003561A patent/KR840001130A/ko not_active Ceased
1985
- 1985-04-04 US US06/719,632 patent/US4649212A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
HU189165B (en)	1986-06-30
DD210256A5 (de)	1984-06-06
EP0072348B1 (de)	1986-03-05
IL66472A (en)	1987-02-27
US4649212A (en)	1987-03-10
PT75390B (en)	1985-11-15
PL141197B1 (en)	1987-07-31
ES514791A0 (es)	1983-11-16
IL66472A0 (en)	1982-12-31
CS245775B2 (en)	1986-10-16
NZ201519A (en)	1985-12-13
ZW16182A1 (en)	1983-03-09
DK354282A (da)	1983-02-08
GB2105715B (en)	1985-09-04
TR21541A (tr)	1984-12-28
PL237790A1 (en)	1984-09-10
BR8204648A (pt)	1983-08-02
EP0072348A2 (de)	1983-02-16
ES8400733A1 (es)	1983-11-16
EP0072348A3 (en)	1983-05-04
KR840001130A (ko)	1984-03-28
GB2105715A (en)	1983-03-30
PT75390A (en)	1982-09-01
GR77261B (cs)	1984-09-11
AU8692382A (en)	1983-02-10
DE3269621D1 (en)	1986-04-10
MA19610A1 (fr)	1983-04-01

Publication	Publication Date	Title
EP0017931B1 (de)	1984-03-07	4H-3,1-Benzoxazinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE69635363T2 (de)	2006-07-27	Fungizide Verfahren, Verbindungen und Zusammensetzungen die Benzophenone enthalten
DE2649706C2 (de)	1982-06-09	ß-[4-(Pyridyl-2-oxy)phenoxy] - propanderivate und Herbicide, welche diese enthalten
DE2661042C2 (cs)	1989-11-09
EP0353187A2 (de)	1990-01-31	Neue Herbizide
DE69126836T2 (de)	1998-01-02	Herbizide
EP0144748A2 (de)	1985-06-19	Imidazolinone, Verfahren zur ihrer Herstellung und ihre Verwendung im Pflanzenschutz
DE2911865C2 (de)	1983-01-13	N-Halogenacetyl-phenylamino-carbonyl-oxime, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Mittel zur Bekämpfung von Unkraut
EP0037925B1 (de)	1983-06-22	Substituierte Pyridazone, Verfahren zu ihrer Herstellung, diese enthaltende Herbizide und ihre Anwendung als Herbizide
EP0103537B1 (de)	1987-07-08	N-Arylsulfonyl-N'-triazolylharnstoffe
CH640108A5 (de)	1983-12-30	Unkrautvernichtungsmittel.
DE1542943C3 (de)	1976-01-08	Benzonitrilderivate und diese enthaltende herbizide Zusammensetzungen
DD204607A5 (de)	1983-12-07	Herbizide und wachstumsregulierende mittel
EP0072348B1 (de)	1986-03-05	Neue Phenoxyphenyl-aminosäure-Derivate, ihre Herstellung, sie enthaltende Mittel sowie ihre Verwendung
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
EP0007089B1 (de)	1981-09-16	Acylanilide mit herbicider und fungicider Wirkung, Verfahren zu ihrer Herstellung und ihre Verwendung
EP0259265B1 (de)	1991-09-11	3-Methylphthalimide
DD157292A5 (de)	1982-11-03	Mittel zur behandlung von pilzinfektionen
DE3239449A1 (de)	1983-05-05	Phenoxyphenyl- und pyridyloxyphenyl-derivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung
EP0071572B1 (de)	1985-08-28	Derivate der 2-Nitro-4- oder 5-Pyridyloxy-phenylphosphonsäure, Verfahren zu ihrer Herstellung, ihre Verwendung als Herbizide und/oder Pflanzenwachstumsregulatoren und/oder Mikrobizide, sowie zur Herstellung der Derivate verwendete Zwischenprodukte, Verfahren zu deren Herstellung und deren Verwendung als Herbizide
EP0030702A1 (de)	1981-06-24	Propionsäureester, Herstellung dieser Verbindungen, Unkrautbekämpfungsmittel, die diese Verbindungen als Wirkstoffe enthalten sowie Verwendung solcher Verbindungen und Mittel zur Bekämpfung von Unkräutern
DE3943015A1 (de)	1990-06-28	Neues herbizides mittel
EP0149427A1 (de)	1985-07-24	(Poly-)Oxyalkylamino-diphenyläther mit herbizider Wirkung
DE2163381A1 (de)	1972-07-27	Herbizide Komposition
EP0069055B1 (de)	1986-12-17	Dihydropyrone, Verfahren zu ihrer Herstellung, Mittel, welche die Dihydropyrone als Wirkstoffe enthalten, und ihre Verwendung zur Bekämpfung von Unkräutern