DD141773A5 - Herbizides mittel - Google Patents

Herbizides mittel Download PDF

Info

Publication number: DD141773A5
Authority: DD; German Democratic Republic
Prior art keywords: parts; formula; weeds; cyanomethyl ester; active
Prior art date: 1978-02-03

Application number

DD79210763A

Other languages

German (de)

English (en)

Inventor

Beat Boehner

Otto Rohr

Original Assignee

Ciba Geigy 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.)

1978-02-03

Filing date

1979-02-01

Publication date

1980-05-21

1979-02-01 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1980-05-21 Publication of DD141773A5 publication Critical patent/DD141773A5/de

Links

239000004009 herbicide Substances 0.000 title description 6
-1 trifluoromethylphenyl Chemical group 0.000 claims description 18
241000196324 Embryophyta Species 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 13
230000002363 herbicidal effect Effects 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 8
238000000034 method Methods 0.000 claims description 7
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 6
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims description 6
235000021536 Sugar beet Nutrition 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 6
235000010469 Glycine max Nutrition 0.000 claims description 5
241001148683 Zostera marina Species 0.000 claims description 5
244000068988 Glycine max Species 0.000 claims description 3
239000000969 carrier Substances 0.000 claims description 3
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
239000004480 active ingredient Substances 0.000 description 14
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
150000002148 esters Chemical class 0.000 description 8
239000013543 active substance Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
239000005995 Aluminium silicate Substances 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
235000012211 aluminium silicate Nutrition 0.000 description 6
239000012141 concentrate Substances 0.000 description 6
239000000839 emulsion Substances 0.000 description 6
239000008187 granular material Substances 0.000 description 6
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 6
238000002360 preparation method Methods 0.000 description 6
241000209764 Avena fatua Species 0.000 description 5
239000000243 solution Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
235000007320 Avena fatua Nutrition 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
241000219146 Gossypium Species 0.000 description 4
239000002202 Polyethylene glycol Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
229920000742 Cotton Polymers 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000004563 wettable powder Substances 0.000 description 3
SXERGJJQSKIUIC-UHFFFAOYSA-N 2-Phenoxypropionic acid Chemical compound OC(=O)C(C)OC1=CC=CC=C1 SXERGJJQSKIUIC-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000000370 acceptor Substances 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
230000006378 damage Effects 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 2
238000009472 formulation Methods 0.000 description 2
LTYRAPJYLUPLCI-UHFFFAOYSA-N glycolonitrile Chemical compound OCC#N LTYRAPJYLUPLCI-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
235000021374 legumes Nutrition 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000012958 reprocessing Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
DQLGAEXVPDFXEU-UHFFFAOYSA-N 2-bromopropanoic acid;hydrobromide Chemical compound Br.CC(Br)C(O)=O DQLGAEXVPDFXEU-UHFFFAOYSA-N 0.000 description 1
FJFSSESWAFPCSU-UHFFFAOYSA-N 4-[4-(trifluoromethyl)phenoxy]phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(C(F)(F)F)C=C1 FJFSSESWAFPCSU-UHFFFAOYSA-N 0.000 description 1
241000743985 Alopecurus Species 0.000 description 1
241001621841 Alopecurus myosuroides Species 0.000 description 1
241001647031 Avena sterilis Species 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
235000021533 Beta vulgaris Nutrition 0.000 description 1
241000209200 Bromus Species 0.000 description 1
241001148727 Bromus tectorum Species 0.000 description 1
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
241000251730 Chondrichthyes Species 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
241000219112 Cucumis Species 0.000 description 1
235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
240000008067 Cucumis sativus Species 0.000 description 1
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
244000285774 Cyperus esculentus Species 0.000 description 1
235000005853 Cyperus esculentus Nutrition 0.000 description 1
102100035861 Cytosolic 5'-nucleotidase 1A Human genes 0.000 description 1
235000017896 Digitaria Nutrition 0.000 description 1
241001303487 Digitaria <clam> Species 0.000 description 1
244000152970 Digitaria sanguinalis Species 0.000 description 1
235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
241000192043 Echinochloa Species 0.000 description 1
244000058871 Echinochloa crus-galli Species 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Natural products OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
235000009438 Gossypium Nutrition 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
101000802744 Homo sapiens Cytosolic 5'-nucleotidase 1A Proteins 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
241000209082 Lolium Species 0.000 description 1
240000004296 Lolium perenne Species 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000857233 Rottboellia Species 0.000 description 1
240000001451 Rottboellia cochinchinensis Species 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
240000005498 Setaria italica Species 0.000 description 1
235000007226 Setaria italica Nutrition 0.000 description 1
241000219793 Trifolium Species 0.000 description 1
FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
SXQXMCWCWVCFPC-UHFFFAOYSA-N aluminum;potassium;dioxido(oxo)silane Chemical compound [Al+3].[K+].[O-][Si]([O-])=O.[O-][Si]([O-])=O SXQXMCWCWVCFPC-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
235000019993 champagne Nutrition 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
244000038559 crop plants Species 0.000 description 1
IMZAAEKPTYNSQK-UHFFFAOYSA-N cyanomethyl 2-bromopropanoate Chemical compound CC(Br)C(=O)OCC#N IMZAAEKPTYNSQK-UHFFFAOYSA-N 0.000 description 1
230000000593 degrading effect Effects 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000002366 halogen compounds Chemical class 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000009528 severe injury Effects 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000000429 sodium aluminium silicate Substances 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000010998 test method Methods 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/14—Preparation of carboxylic acid nitriles by reaction of cyanides with halogen-containing compounds with replacement of halogen atoms by cyano groups
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof

Landscapes

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

DD79210763A 1978-02-03 1979-02-01 Herbizides mittel DD141773A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH121478		1978-02-03

Publications (1)

Publication Number	Publication Date
DD141773A5 true DD141773A5 (de)	1980-05-21

Family

ID=4205165

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79210763A DD141773A5 (de)	1978-02-03	1979-02-01	Herbizides mittel

Country Status (18)

Country	Link
US (1)	US4226614A (fr)
EP (1)	EP0003517B1 (fr)
JP (1)	JPS54115333A (fr)
KR (1)	KR820002294B1 (fr)
AT (1)	AT361247B (fr)
BG (1)	BG29123A3 (fr)
BR (1)	BR7900650A (fr)
CA (1)	CA1097681A (fr)
CS (1)	CS203944B2 (fr)
DD (1)	DD141773A5 (fr)
DE (1)	DE2960206D1 (fr)
ES (1)	ES477400A1 (fr)
HU (1)	HU182476B (fr)
IL (1)	IL56563A (fr)
MX (1)	MX5372E (fr)
PL (1)	PL121432B1 (fr)
RO (1)	RO76294A (fr)
ZA (1)	ZA79443B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2446812A1 (fr) *	1979-01-16	1980-08-14	Produits Ind Cie Fse	Phenoxy- et thiophenoxynitriles et leurs applications en tant qu'herbicides
FR2473514A2 (fr) *	1980-01-15	1981-07-17	Produits Ind Cie Fse	Phenoxy- et thiophenoxynitriles et leurs applications en tant qu'herbicides
DE3779099D1 (de) *	1987-02-05	1992-06-17	Ppg Industries Inc	Substituierte phenoxypropionaldehydderivate.
GB0002280D0 (en) *	2000-02-02	2000-03-22	Gault Norman	A device for controlling fish lice populations

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL136904C (fr)	1962-02-08
US3702862A (en)	1968-03-13	1972-11-14	Sumitomo Chemical Co	Alkyl- and halo-substituted phenoxy benzonitriles
US3928416A (en)	1972-03-14	1975-12-23	Rohm & Haas	Herbicidal 4-trifluoromethyl-4{40 nitrodiphenyl ethers
GB1560416A (en)	1975-09-03	1980-02-06	Rohm & Haas	Trifluoromethylphenyl derivatives
DE2613697A1 (de)	1976-03-31	1977-10-13	Hoechst Ag	Herbizide mittel
DE2613645B2 (de)	1976-03-31	1979-09-06	W.C. Heraeus Gmbh, 6450 Hanau	Verfahren zur Hydrierung von Zimtaldehyden
US4071178A (en) *	1976-06-07	1978-01-31	Copp Robert M	Machine for use with moving webs
DE2628384C2 (de)	1976-06-24	1984-09-27	Hoechst Ag, 6230 Frankfurt	2-(4-Phenoxyphenoxy)- bzw. 2-(4-Benzylphenoxy)-propionsäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenbehandlungsmittel
US4059435A (en)	1976-08-31	1977-11-22	Rohm And Haas Company	Herbicidal 4-trifluoromethyl-3-cyanoalkoxy-4-nitro diphenyl ethers

1979
- 1979-01-22 EP EP79100172A patent/EP0003517B1/fr not_active Expired
- 1979-01-22 DE DE7979100172T patent/DE2960206D1/de not_active Expired
- 1979-01-29 RO RO7996426A patent/RO76294A/fr unknown
- 1979-02-01 BG BG042330A patent/BG29123A3/xx unknown
- 1979-02-01 DD DD79210763A patent/DD141773A5/de unknown
- 1979-02-01 US US06/008,624 patent/US4226614A/en not_active Expired - Lifetime
- 1979-02-01 CS CS79723A patent/CS203944B2/cs unknown
- 1979-02-01 IL IL56563A patent/IL56563A/xx unknown
- 1979-02-01 CA CA320,726A patent/CA1097681A/fr not_active Expired
- 1979-02-01 MX MX797699U patent/MX5372E/es unknown
- 1979-02-02 JP JP1181479A patent/JPS54115333A/ja active Pending
- 1979-02-02 ES ES477400A patent/ES477400A1/es not_active Expired
- 1979-02-02 HU HU79CI1909A patent/HU182476B/hu unknown
- 1979-02-02 KR KR7900305A patent/KR820002294B1/ko not_active Expired
- 1979-02-02 PL PL1979213148A patent/PL121432B1/pl unknown
- 1979-02-02 BR BR7900650A patent/BR7900650A/pt unknown
- 1979-02-02 AT AT80279A patent/AT361247B/de not_active IP Right Cessation
- 1979-02-02 ZA ZA79443A patent/ZA79443B/xx unknown

Also Published As

Publication number	Publication date
EP0003517A1 (fr)	1979-08-22
CS203944B2 (en)	1981-03-31
KR820002294B1 (ko)	1982-12-15
MX5372E (es)	1983-06-30
AT361247B (de)	1981-02-25
PL121432B1 (en)	1982-05-31
IL56563A (en)	1982-09-30
BG29123A3 (en)	1980-09-15
RO76294A (fr)	1981-04-30
ATA80279A (de)	1980-07-15
HU182476B (en)	1984-01-30
CA1097681A (fr)	1981-03-17
ES477400A1 (es)	1980-01-16
EP0003517B1 (fr)	1981-03-25
IL56563A0 (en)	1979-05-31
BR7900650A (pt)	1979-08-28
PL213148A1 (fr)	1980-07-01
US4226614A (en)	1980-10-07
ZA79443B (en)	1980-02-27
JPS54115333A (en)	1979-09-07
DE2960206D1 (en)	1981-04-16

Publication	Publication Date	Title
EP0003114B1 (fr)	1982-01-27	Esters insaturés à activité herbicide d'acides 4- (3',5'-dihalogéno-pyridyl -(2')-oxy)-alpha-phénoxypropionique, procédé de leur préparation, compositions herbicides les contenant et leur utilisation
DE2617804C2 (de)	1985-01-24	2-(4-Phenoxy phenoxy)-propionsäurederivate und ihre Verwendung als Herbizide
EP0083556A2 (fr)	1983-07-13	Dérivés d'acide alpha-(4-(3'-fluor-5'-halogène-pyridyl-2'-oxy)-phenoxy)propionique avec activité herbicide
DD149013A5 (de)	1981-06-24	Herbizides und pflanzenregulierendes mittel
EP0248968A1 (fr)	1987-12-16	Ester propynylique de l'acide (R)-2-[4-(5-chloro-3-fluoropyridine-2-yloxy)-phénoxy]-propionique à activité herbicide
EP0039310A2 (fr)	1981-11-04	Acide phosphonométhylglycylhydroxamique et leurs sels, leur préparation et utilisation dans des compositions herbicides
DE2652384A1 (de)	1977-05-26	Neue herbizid wirksame, kernsubstituierte phenoxy-phenoxy-alkancarbonsaeurederivate und deren verwendung zur bekaempfung von ungraesern
EP0075840B1 (fr)	1987-11-11	Phényléthers hétérocycliques, procédé pour leur préparation et herbicides les contenant
CH626777A5 (en)	1981-12-15	Herbicide
EP0002812B1 (fr)	1982-02-03	Phénoxyalcoyloxazolines, leur préparation, compositions les contenant et leur application comme herbicides
EP0058639B1 (fr)	1985-08-14	Esters de l'acide 2-(4-(6-halogène-quinoxalinyl-2-oxy)-phénoxy)-propionique, leurs procédés de préparation et leur application comme herbicides et régulateurs de la croissance de plantes
EP0007089B1 (fr)	1981-09-16	Acylanilides à activité herbicide et fungicide, procédé pour leur préparation et leur utilisation
DD141773A5 (de)	1980-05-21	Herbizides mittel
EP0001641B1 (fr)	1981-11-18	Ester methoxyethylique de l'acide 2(2'-Nitro-5-(2"-chloro-4" trifluoromethylphenoxy)-phenoxy) propionique, une composition contenant cet ester comme substance active, et son utilisation comme herbicide.
EP0003059B1 (fr)	1981-01-07	Alcoxyalcoylamides de l'acide 4-(p-phénoxy-phénoxy)-alpha-propionique, doués d'une activité herbicide, procédé pour leur préparation et agents herbicides les contenant et leur usage
DE2732442A1 (de)	1978-01-26	Neue phenoxy-phenoxy-alkancarbonsaeurederivate
DE3018003C2 (fr)	1989-07-13
EP0203607B1 (fr)	1988-08-31	Esters de l'acide benzoique, procédés pour leur préparation et leur utilisation pour la lutte contre les parasites
EP0171724A2 (fr)	1986-02-19	Dérivés de l'acide phénoxypropionique, procédé pour leur préparation et leur utilisation comme herbicides
EP0149427B1 (fr)	1987-07-08	(Poly-)Oxyalkylaminodiphényloxydes à activité herbicide
EP0003297A1 (fr)	1979-08-08	Phenoxy-alcoyl-oxazolines, leur préparation, compositions herbicides les contenant et leur application
EP0075249B1 (fr)	1985-02-13	Agents herbicides
EP0005709B1 (fr)	1981-12-09	Dérivés d'éther diphénylique ayant une activité herbicide, les compositions herbicides en contenant et leurs utilisations
EP0071572A2 (fr)	1983-02-09	Dérivés de l'acide nitro-2 pyridyloxy-4 ou -5 phosphonique, leur procédé de préparation, leur utilisation comme herbicides et/ou régulateurs de la croissance des plantes et/ou microbicides, ainsi que les intermédiaires utilisés pour leur préparation, leur procédé de préparation et leur utilisation comme herbicides
DE2163381A1 (de)	1972-07-27	Herbizide Komposition