NL8105358A - N-halogeenacetyl-2-gesubstitueerde-6-acylanilinen, werkwijzen ter bereiding ervan alsmede hun toepassing als herbicide. - Google Patents

N-halogeenacetyl-2-gesubstitueerde-6-acylanilinen, werkwijzen ter bereiding ervan alsmede hun toepassing als herbicide. Download PDF

Info

Publication number: NL8105358A
Authority: NL; Netherlands
Prior art keywords: carbon atoms; alkyl; hydrogen; compound according; groups
Prior art date: 1980-12-01

Application number

NL8105358A

Other languages

English (en)

Dutch (nl)

Original Assignee

Chevron Res

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.)

1980-12-01

Filing date

1981-11-26

Publication date

1982-07-01

1981-11-26 Application filed by Chevron Res filed Critical Chevron Res

1982-07-01 Publication of NL8105358A publication Critical patent/NL8105358A/nl

Links

230000002363 herbicidal effect Effects 0.000 title claims description 18
238000000034 method Methods 0.000 title claims description 12
239000004009 herbicide Substances 0.000 title description 12
150000001875 compounds Chemical class 0.000 claims description 41
125000004432 carbon atom Chemical group C* 0.000 claims description 29
125000000217 alkyl group Chemical group 0.000 claims description 24
229910052739 hydrogen Inorganic materials 0.000 claims description 21
239000001257 hydrogen Substances 0.000 claims description 21
239000000203 mixture Substances 0.000 claims description 17
241000196324 Embryophyta Species 0.000 claims description 15
230000008635 plant growth Effects 0.000 claims description 12
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
230000000979 retarding effect Effects 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
230000012010 growth Effects 0.000 claims description 5
229910052760 oxygen Inorganic materials 0.000 claims description 5
239000001301 oxygen Substances 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
235000005474 African couch grass Nutrition 0.000 claims description 2
241001520106 Eustachys Species 0.000 claims description 2
241000234642 Festuca Species 0.000 claims description 2
241000209049 Poa pratensis Species 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000004122 cyclic group Chemical group 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
239000007788 liquid Substances 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
-1 methoxyethyl Chemical group 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000000843 powder Substances 0.000 description 7
239000000047 product Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
239000000243 solution Substances 0.000 description 7
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
150000002431 hydrogen Chemical class 0.000 description 4
239000002689 soil Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
244000025254 Cannabis sativa Species 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000004480 active ingredient Substances 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052794 bromium Inorganic materials 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000009472 formulation Methods 0.000 description 3
229910052943 magnesium sulfate Inorganic materials 0.000 description 3
235000019341 magnesium sulphate Nutrition 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
230000001105 regulatory effect Effects 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
SIAKXVRAWQIXRD-UHFFFAOYSA-N 1-(2-amino-3-methylphenyl)ethanone Chemical compound CC(=O)C1=CC=CC(C)=C1N SIAKXVRAWQIXRD-UHFFFAOYSA-N 0.000 description 2
240000006122 Chenopodium album Species 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
231100000674 Phytotoxicity Toxicity 0.000 description 2
241000209504 Poaceae Species 0.000 description 2
239000002250 absorbent Substances 0.000 description 2
230000002745 absorbent Effects 0.000 description 2
230000033228 biological regulation Effects 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
230000009036 growth inhibition Effects 0.000 description 2
238000002156 mixing Methods 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
KSYYGSHRSYRNID-UHFFFAOYSA-N n-(2-acetyl-6-methylphenyl)-2-chloroacetamide Chemical compound CC(=O)C1=CC=CC(C)=C1NC(=O)CCl KSYYGSHRSYRNID-UHFFFAOYSA-N 0.000 description 2
238000003359 percent control normalization Methods 0.000 description 2
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
235000013772 propylene glycol Nutrition 0.000 description 2
241000894007 species Species 0.000 description 2
239000012085 test solution Substances 0.000 description 2
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
244000237956 Amaranthus retroflexus Species 0.000 description 1
235000013479 Amaranthus retroflexus Nutrition 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
244000078782 Brassica arvensis Species 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
244000056139 Brassica cretica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
235000011498 Chenopodium album var missouriense Nutrition 0.000 description 1
235000013328 Chenopodium album var. album Nutrition 0.000 description 1
235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 1
235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 1
235000013012 Chenopodium album var. striatum Nutrition 0.000 description 1
244000300310 Chenopodium rubrum Species 0.000 description 1
235000009332 Chenopodium rubrum Nutrition 0.000 description 1
VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
244000152970 Digitaria sanguinalis Species 0.000 description 1
235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241000209082 Lolium Species 0.000 description 1
240000008790 Musa x paradisiaca Species 0.000 description 1
235000018290 Musa x paradisiaca Nutrition 0.000 description 1
RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
244000062793 Sorghum vulgare Species 0.000 description 1
235000005373 Uvularia sessilifolia Nutrition 0.000 description 1
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
230000021736 acetylation Effects 0.000 description 1
238000006640 acetylation reaction Methods 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
XPHBRTNHVJSEQD-UHFFFAOYSA-N anidoxime Chemical compound C=1C=CC=CC=1C(CCN(CC)CC)=NOC(=O)NC1=CC=C(OC)C=C1 XPHBRTNHVJSEQD-UHFFFAOYSA-N 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
210000001217 buttock Anatomy 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000000378 calcium silicate Substances 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
125000002837 carbocyclic group Chemical group 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical class NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
239000004927 clay Substances 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
229940125782 compound 2 Drugs 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
230000006196 deacetylation Effects 0.000 description 1
238000003381 deacetylation reaction Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
239000000284 extract Substances 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
230000003862 health status Effects 0.000 description 1
235000008216 herbs Nutrition 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
239000002917 insecticide 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
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000005907 ketalization reaction Methods 0.000 description 1
210000002414 leg Anatomy 0.000 description 1
210000001699 lower leg Anatomy 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
230000000877 morphologic effect Effects 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
VUUGAGWCSSOPDZ-UHFFFAOYSA-N n-(2-acetyl-6-methylphenyl)acetamide Chemical compound CC(=O)NC1=C(C)C=CC=C1C(C)=O VUUGAGWCSSOPDZ-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
UAJUXJSXCLUTNU-UHFFFAOYSA-N pranlukast Chemical compound C=1C=C(OCCCCC=2C=CC=CC=2)C=CC=1C(=O)NC(C=1)=CC=C(C(C=2)=O)C=1OC=2C=1N=NNN=1 UAJUXJSXCLUTNU-UHFFFAOYSA-N 0.000 description 1
229960004583 pranlukast Drugs 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
238000010992 reflux Methods 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
239000000377 silicon dioxide Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
- A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
- A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
- A01N43/30—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
- 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
- A01N43/74—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 five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
- 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
- A01N43/86—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/28—Radicals substituted by nitrogen atoms

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NL8105358A 1980-12-01 1981-11-26 N-halogeenacetyl-2-gesubstitueerde-6-acylanilinen, werkwijzen ter bereiding ervan alsmede hun toepassing als herbicide. NL8105358A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US21161880A	1980-12-01	1980-12-01
US21161880		1980-12-01

Publications (1)

Publication Number	Publication Date
NL8105358A true NL8105358A (nl)	1982-07-01

Family

ID=22787669

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8105358A NL8105358A (nl)	1980-12-01	1981-11-26	N-halogeenacetyl-2-gesubstitueerde-6-acylanilinen, werkwijzen ter bereiding ervan alsmede hun toepassing als herbicide.

Country Status (10)

Country	Link
JP (1)	JPS57120585A (fr)
AU (1)	AU557690B2 (fr)
BE (1)	BE891302A (fr)
CA (1)	CA1195994A (fr)
CH (1)	CH648304A5 (fr)
DE (1)	DE3147155A1 (fr)
FR (1)	FR2495152B1 (fr)
GB (1)	GB2088380B (fr)
IL (1)	IL64223A (fr)
NL (1)	NL8105358A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3926898A1 (de) *	1989-08-16	1991-02-21	Thomae Gmbh Dr K	Neue 1,3-oxazine

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4244730A (en) *	1979-07-02	1981-01-13	Chevron Research Company	Herbicidal N-haloacetyl-2-alkyl-6-acylanilines

1981
- 1981-11-06 IL IL64223A patent/IL64223A/xx unknown
- 1981-11-23 FR FR8121872A patent/FR2495152B1/fr not_active Expired
- 1981-11-26 CA CA000391008A patent/CA1195994A/fr not_active Expired
- 1981-11-26 NL NL8105358A patent/NL8105358A/nl not_active Application Discontinuation
- 1981-11-27 DE DE19813147155 patent/DE3147155A1/de not_active Withdrawn
- 1981-11-27 AU AU77957/81A patent/AU557690B2/en not_active Ceased
- 1981-11-30 CH CH7667/81A patent/CH648304A5/de not_active IP Right Cessation
- 1981-11-30 JP JP56192681A patent/JPS57120585A/ja active Pending
- 1981-11-30 BE BE0/206702A patent/BE891302A/fr not_active IP Right Cessation
- 1981-12-01 GB GB8136191A patent/GB2088380B/en not_active Expired

Also Published As

Publication number	Publication date
BE891302A (fr)	1982-03-16
GB2088380B (en)	1984-08-15
CH648304A5 (de)	1985-03-15
DE3147155A1 (de)	1982-07-29
AU7795781A (en)	1982-06-10
IL64223A0 (en)	1982-02-28
AU557690B2 (en)	1987-01-08
CA1195994A (fr)	1985-10-29
JPS57120585A (en)	1982-07-27
GB2088380A (en)	1982-06-09
FR2495152A1 (fr)	1982-06-04
FR2495152B1 (fr)	1985-12-13
IL64223A (en)	1985-11-29

Legal Events

Date	Code	Title	Description
1985-01-01	A85	Still pending on 85-01-01
1989-01-02	BV	The patent application has lapsed

Publication	Publication Date	Title
EP0239414B1 (fr)	1989-11-02	Amide N-benzylique de l'acide 2-(4-fluoro-3-trifluorométhylphénoxy)butanoique et composition herbicide le contenant
SU656465A3 (ru)	1979-04-05	Гербицидное средство
NL192263C (nl)	1997-04-03	Gesubstitueerde 1,3-cyclohexaandionoximderivaten met herbicide werking, alsmede herbicide preparaten, die deze verbindingen bevatten.
CA1158257A (fr)	1983-12-06	Derives de cyclohexane
US4626276A (en)	1986-12-02	Herbicidal trans-2-[(3-chloroallyloxyimino)alkyl]-5-(substitutedsulfinylalkyl)-cyclohexane-1,3-diones and derivatives thereof
NL193944C (nl)	2001-03-02	Onkruidbestrijdingsmiddelen op basis van 2- 1-(3-chloorallyloxyamino)-alkylideen -5-alkylthioalkyl-1,3-cyclohexaandion.
US4259104A (en)	1981-03-31	Herbicidal and plant-growth-regulating 2-phenoxyalkyl-oxadiazoles
NL8105358A (nl)	1982-07-01	N-halogeenacetyl-2-gesubstitueerde-6-acylanilinen, werkwijzen ter bereiding ervan alsmede hun toepassing als herbicide.
JPH0130818B2 (fr)	1989-06-22
US4551478A (en)	1985-11-05	3-Nitrobenzene sulfonanilide derivatives and fungicidal compositions for the control of plant diseases containing same
DE3300056C2 (de)	1985-06-27	3-Nitrobenzolsulfonanilid-Derivate und diese enthaltende fungizide Mittel
JP2871113B2 (ja)	1999-03-17	除草用組成物
US4174210A (en)	1979-11-13	Herbicidal and plant-growth regulating N-haloacetylphenylamino carbonyl oximes
US4465502A (en)	1984-08-14	Herbicidal N-haloacetyl-2-substituted-6-acylanilines
US4468247A (en)	1984-08-28	Herbicidal 4-[3'-(4"-trifluoromethyl-phenoxy)-phenoxy]-4-methyl-crotonates
US3099658A (en)	1963-07-30	Thianaphthene 1,1-dioxide compounds
GB2060634A (en)	1981-05-07	Herbicidally Active 2-nitro- styrene Derivatives
JPS6012353B2 (ja)	1985-04-01	２−（置換フエノキシ）プロピオン酸誘導体及びそれを有効成分とする除草剤
JPS637534B2 (fr)	1988-02-17
CA1059133A (fr)	1979-07-24	Les n-haloacyl (derive 4 et 5-spirocycloaliphatique) oxazolidines
EP0262265A1 (fr)	1988-04-06	Dérivés de cyclohexane-1,2-dione substituée à activité herbicide
JPS61204105A (ja)	1986-09-10	稲いもち病防除剤
JPS6368558A (ja)	1988-03-28	シクロヘキサン−１，３−ジオン化合物、その製造法および除草剤組成物
JPS6339859A (ja)	1988-02-20	イソインド−ル誘導体、その製造方法及び除草剤
GB2103612A (en)	1983-02-23	Herbicidal disubstituted N-haloacetylaniline compounds