DE2711928A1 - Acetanilidderivate, sie enthaltende herbizide mittel und ihre verwendung - Google Patents

Acetanilidderivate, sie enthaltende herbizide mittel und ihre verwendung

Info

Publication number: DE2711928A1
Authority: DE; Germany
Prior art keywords: tert; butyl; acetanilide; compounds; group
Prior art date: 1976-03-19
Legal status (The legal status 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 status listed.): Pending

Application number

DE19772711928

Other languages

German (de)

English (en)

Inventor

John Paul Chupp

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Monsanto Co

Original Assignee

Monsanto Co

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.)

1976-03-19

Filing date

1977-03-18

Publication date

1977-10-06

1977-03-18 Application filed by Monsanto Co filed Critical Monsanto Co

1977-10-06 Publication of DE2711928A1 publication Critical patent/DE2711928A1/de

Status Pending legal-status Critical Current

Links

230000002363 herbicidal effect Effects 0.000 title claims description 33
FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical class CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 title claims description 13
150000001875 compounds Chemical class 0.000 claims description 134
241000196324 Embryophyta Species 0.000 claims description 41
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims description 32
235000021536 Sugar beet Nutrition 0.000 claims description 32
125000000217 alkyl group Chemical group 0.000 claims description 27
239000000203 mixture Substances 0.000 claims description 22
125000005843 halogen group Chemical group 0.000 claims description 19
238000000034 method Methods 0.000 claims description 19
-1 tert-butyl-2,6'-dichloro-N- (isobutoxymethyl) acetanilide Chemical compound 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 15
229960001413 acetanilide Drugs 0.000 claims description 14
229910052740 iodine Inorganic materials 0.000 claims description 9
150000008061 acetanilides Chemical class 0.000 claims description 7
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
125000001309 chloro group Chemical group Cl* 0.000 claims description 6
244000068988 Glycine max Species 0.000 claims description 5
235000010469 Glycine max Nutrition 0.000 claims description 5
240000007594 Oryza sativa Species 0.000 claims description 5
235000007164 Oryza sativa Nutrition 0.000 claims description 5
235000011684 Sorghum saccharatum Nutrition 0.000 claims description 5
125000003342 alkenyl group Chemical group 0.000 claims description 5
235000009566 rice Nutrition 0.000 claims description 5
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
240000006394 Sorghum bicolor Species 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
125000000304 alkynyl group Chemical group 0.000 claims description 3
229910052731 fluorine Inorganic materials 0.000 claims description 3
125000001153 fluoro group Chemical group F* 0.000 claims description 3
230000012010 growth Effects 0.000 claims description 3
RKAMAEHVSGTUEI-UHFFFAOYSA-N C(C)(C)(C)C1=C(N(C(CCl)=O)COC(C)C)C(=CC=C1)Cl Chemical compound C(C)(C)(C)C1=C(N(C(CCl)=O)COC(C)C)C(=CC=C1)Cl RKAMAEHVSGTUEI-UHFFFAOYSA-N 0.000 claims description 2
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
244000045561 useful plants Species 0.000 claims description 2
TUEZZFCIJOJMLB-UHFFFAOYSA-N CCCCC(C(N(COCC)C1=CC=CC=C1Cl)=O)Br Chemical compound CCCCC(C(N(COCC)C1=CC=CC=C1Cl)=O)Br TUEZZFCIJOJMLB-UHFFFAOYSA-N 0.000 claims 1
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235000001155 Setaria leucopila Nutrition 0.000 description 21
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VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
240000001592 Amaranthus caudatus Species 0.000 description 20
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 20
235000009328 Amaranthus caudatus Nutrition 0.000 description 19
239000008280 blood Substances 0.000 description 18
210000004369 blood Anatomy 0.000 description 18
239000004009 herbicide Substances 0.000 description 18
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 14
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UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
206010011878 Deafness Diseases 0.000 description 12
230000005764 inhibitory process Effects 0.000 description 12
239000004480 active ingredient Substances 0.000 description 11
238000004458 analytical method Methods 0.000 description 11
239000000463 material Substances 0.000 description 11
241000272201 Columbiformes Species 0.000 description 10
229910052757 nitrogen Inorganic materials 0.000 description 10
239000003921 oil Substances 0.000 description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
241000287828 Gallus gallus Species 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
150000003931 anilides Chemical class 0.000 description 9
239000002904 solvent Substances 0.000 description 9
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
239000000243 solution Substances 0.000 description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
239000000460 chlorine Substances 0.000 description 7
238000002844 melting Methods 0.000 description 7
230000008018 melting Effects 0.000 description 7
239000000047 product Substances 0.000 description 7
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 7
239000007787 solid Substances 0.000 description 7
VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 6
PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
230000000052 comparative effect Effects 0.000 description 5
125000004433 nitrogen atom Chemical group N* 0.000 description 5
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 5
238000001953 recrystallisation Methods 0.000 description 5
SSKOQDSCQVSEGT-UHFFFAOYSA-N 2-tert-butyl-6-chloroaniline Chemical compound CC(C)(C)C1=CC=CC(Cl)=C1N SSKOQDSCQVSEGT-UHFFFAOYSA-N 0.000 description 4
235000011293 Brassica napus Nutrition 0.000 description 4
240000008100 Brassica rapa Species 0.000 description 4
235000000540 Brassica rapa subsp rapa Nutrition 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
244000239348 Echinochloa crus galli var. praticola Species 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
238000009472 formulation Methods 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
244000058871 Echinochloa crus-galli Species 0.000 description 3
241000209510 Liliopsida Species 0.000 description 3
MHIUHSXAIQZNPU-UHFFFAOYSA-N N-(2-tert-butyl-6-chlorophenyl)-2-chloro-N-(methoxymethyl)acetamide Chemical compound C(C)(C)(C)C1=C(N(C(CCl)=O)COC)C(=CC=C1)Cl MHIUHSXAIQZNPU-UHFFFAOYSA-N 0.000 description 3
229930040373 Paraformaldehyde Natural products 0.000 description 3
241000209504 Poaceae Species 0.000 description 3
235000013339 cereals Nutrition 0.000 description 3
238000004587 chromatography analysis Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
229920002866 paraformaldehyde Polymers 0.000 description 3
231100000208 phytotoxic Toxicity 0.000 description 3
230000000885 phytotoxic effect Effects 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
239000007858 starting material Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
YXNAWCUIZOCJNG-UHFFFAOYSA-N 2-iodo-n-phenylacetamide Chemical class ICC(=O)NC1=CC=CC=C1 YXNAWCUIZOCJNG-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
244000025254 Cannabis sativa Species 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
244000292697 Polygonum aviculare Species 0.000 description 2
235000006386 Polygonum aviculare Nutrition 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
JNGZXGGOCLZBFB-IVCQMTBJSA-N compound E Chemical compound N([C@@H](C)C(=O)N[C@@H]1C(N(C)C2=CC=CC=C2C(C=2C=CC=CC=2)=N1)=O)C(=O)CC1=CC(F)=CC(F)=C1 JNGZXGGOCLZBFB-IVCQMTBJSA-N 0.000 description 2
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238000002425 crystallisation Methods 0.000 description 2
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239000000155 melt Substances 0.000 description 2
GBXKJPOXVQNHEC-UHFFFAOYSA-N n-(2-tert-butyl-6-chlorophenyl)-2-chloroacetamide Chemical compound CC(C)(C)C1=CC=CC(Cl)=C1NC(=O)CCl GBXKJPOXVQNHEC-UHFFFAOYSA-N 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
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239000004094 surface-active agent Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
FOYHNROGBXVLLX-UHFFFAOYSA-N 2,6-diethylaniline Chemical compound CCC1=CC=CC(CC)=C1N FOYHNROGBXVLLX-UHFFFAOYSA-N 0.000 description 1
QFMPPVCBYDNCLP-UHFFFAOYSA-N 2-bromo-n-(2-tert-butyl-6-chlorophenyl)acetamide Chemical class CC(C)(C)C1=CC=CC(Cl)=C1NC(=O)CBr QFMPPVCBYDNCLP-UHFFFAOYSA-N 0.000 description 1
LSTRKXWIZZZYAS-UHFFFAOYSA-N 2-bromoacetyl bromide Chemical compound BrCC(Br)=O LSTRKXWIZZZYAS-UHFFFAOYSA-N 0.000 description 1
QDOJXLUCPMRXBN-UHFFFAOYSA-N 2-chloro-n-(2-chloro-6-methylphenyl)-n-(2-ethoxyethyl)acetamide Chemical compound CCOCCN(C(=O)CCl)C1=C(C)C=CC=C1Cl QDOJXLUCPMRXBN-UHFFFAOYSA-N 0.000 description 1
KNVBYGNINQITJC-UHFFFAOYSA-N 2-chloro-n-(3-chlorophenyl)acetamide Chemical class ClCC(=O)NC1=CC=CC(Cl)=C1 KNVBYGNINQITJC-UHFFFAOYSA-N 0.000 description 1
VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical compound ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 1
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
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BVKHNZOTOHJGID-UHFFFAOYSA-N C(C)(C)(C)C1=C(N(C(CI)=O)COC(C)C)C(=CC=C1)Cl Chemical compound C(C)(C)(C)C1=C(N(C(CI)=O)COC(C)C)C(=CC=C1)Cl BVKHNZOTOHJGID-UHFFFAOYSA-N 0.000 description 1
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235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
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DBLCZNLGZFQPKO-KYIGKLDSSA-M [(e)-3-chlorobut-2-enyl]-dimethyl-[2-oxo-2-(2-phenylethoxy)ethyl]azanium;bromide Chemical compound [Br-].C\C(Cl)=C/C[N+](C)(C)CC(=O)OCCC1=CC=CC=C1 DBLCZNLGZFQPKO-KYIGKLDSSA-M 0.000 description 1
239000002253 acid Substances 0.000 description 1
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XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
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150000001408 amides Chemical class 0.000 description 1
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MMCPOSDMTGQNKG-UJZMCJRSSA-N aniline;hydrochloride Chemical group Cl.N[14C]1=[14CH][14CH]=[14CH][14CH]=[14CH]1 MMCPOSDMTGQNKG-UJZMCJRSSA-N 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
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239000012267 brine Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
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239000000428 dust Substances 0.000 description 1
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
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238000001030 gas--liquid chromatography Methods 0.000 description 1
FVIZARNDLVOMSU-UHFFFAOYSA-N ginsenoside K Natural products C1CC(C2(CCC3C(C)(C)C(O)CCC3(C)C2CC2O)C)(C)C2C1C(C)(CCC=C(C)C)OC1OC(CO)C(O)C(O)C1O FVIZARNDLVOMSU-UHFFFAOYSA-N 0.000 description 1
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Classifications

- 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
- A01N37/22—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 the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
- C07C233/15—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring

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

DE19772711928 1976-03-19 1977-03-18 Acetanilidderivate, sie enthaltende herbizide mittel und ihre verwendung Pending DE2711928A1 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US66877076A	1976-03-19	1976-03-19

Publications (1)

Publication Number	Publication Date
DE2711928A1 true DE2711928A1 (de)	1977-10-06

Family

ID=24683658

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19772711928 Pending DE2711928A1 (de)	1976-03-19	1977-03-18	Acetanilidderivate, sie enthaltende herbizide mittel und ihre verwendung

Country Status (19)

Country	Link
JP (1)	JPS52113927A (sv)
AU (1)	AU2336677A (sv)
BE (1)	BE852621A (sv)
BR (1)	BR7701680A (sv)
CS (1)	CS193088B2 (sv)
DD (1)	DD130905A5 (sv)
DE (1)	DE2711928A1 (sv)
DK (1)	DK120377A (sv)
FR (1)	FR2344524A1 (sv)
GB (1)	GB1546029A (sv)
GR (1)	GR64413B (sv)
IT (1)	IT1113764B (sv)
LU (1)	LU76981A1 (sv)
NL (1)	NL7702888A (sv)
PL (1)	PL103793B1 (sv)
SE (1)	SE7703105L (sv)
SU (1)	SU659065A3 (sv)
TR (1)	TR19420A (sv)
ZA (1)	ZA771642B (sv)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK153543B (da) *	1979-04-24	1988-07-25	Mta Mezoegazdasagi Kutato	Fremgangsmaade til fremstilling af 2',6'-dialkyl-n-alkoxymethyl-2-chlor-acetanilider

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RO85641B (ro) *	1980-03-25	1984-11-30	Monsanto Company	Compozitie erbicida
EP0580741B1 (en) *	1991-04-04	1997-06-04	Zeneca Limited	Process for conducting chemical reactions with formaldehyde

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE788215A (fr) *	1971-09-01	1973-02-28	Ciba Geigy	Haloacetanilides utiles comme herbicides
CH579348A5 (sv) *	1973-02-08	1976-09-15	Ciba Geigy Ag

1977
- 1977-03-15 PL PL1977196669A patent/PL103793B1/pl unknown
- 1977-03-17 TR TR19420A patent/TR19420A/xx unknown
- 1977-03-17 NL NL7702888A patent/NL7702888A/xx not_active Application Discontinuation
- 1977-03-17 IT IT21387/77A patent/IT1113764B/it active
- 1977-03-18 BR BR7701680A patent/BR7701680A/pt unknown
- 1977-03-18 DE DE19772711928 patent/DE2711928A1/de active Pending
- 1977-03-18 JP JP3100477A patent/JPS52113927A/ja active Pending
- 1977-03-18 FR FR7708246A patent/FR2344524A1/fr not_active Withdrawn
- 1977-03-18 BE BE175903A patent/BE852621A/xx unknown
- 1977-03-18 LU LU76981A patent/LU76981A1/xx unknown
- 1977-03-18 CS CS771805A patent/CS193088B2/cs unknown
- 1977-03-18 DD DD7700197927A patent/DD130905A5/xx unknown
- 1977-03-18 SE SE7703105A patent/SE7703105L/sv not_active Application Discontinuation
- 1977-03-18 GR GR53038A patent/GR64413B/el unknown
- 1977-03-18 AU AU23366/77A patent/AU2336677A/en not_active Expired
- 1977-03-18 SU SU772460813A patent/SU659065A3/ru active
- 1977-03-18 GB GB11507/77A patent/GB1546029A/en not_active Expired
- 1977-03-18 DK DK120377A patent/DK120377A/da not_active IP Right Cessation
- 1977-03-18 ZA ZA00771642A patent/ZA771642B/xx unknown

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK153543B (da) *	1979-04-24	1988-07-25	Mta Mezoegazdasagi Kutato	Fremgangsmaade til fremstilling af 2',6'-dialkyl-n-alkoxymethyl-2-chlor-acetanilider

Also Published As

Publication number	Publication date
JPS52113927A (en)	1977-09-24
GB1546029A (en)	1979-05-16
SE7703105L (sv)	1977-09-20
PL103793B1 (pl)	1979-07-31
BE852621A (fr)	1977-09-19
ZA771642B (en)	1978-02-22
TR19420A (tr)	1979-03-19
SU659065A3 (en)	1979-04-25
FR2344524A1 (fr)	1977-10-14
GR64413B (en)	1980-03-21
PL196669A1 (pl)	1978-01-02
DD130905A5 (de)	1978-05-17
DK120377A (da)	1977-09-20
AU2336677A (en)	1978-09-21
LU76981A1 (sv)	1977-10-03
BR7701680A (pt)	1977-11-08
NL7702888A (nl)	1977-09-21
CS193088B2 (en)	1979-09-17
IT1113764B (it)	1986-01-20

Legal Events

Date	Code	Title	Description
1981-01-08	OHJ	Non-payment of the annual fee

Publication	Publication Date	Title
DE3121704C2 (de)	1994-11-17	2-Benzyl-3-isoxazolidinone, Verfahren zu deren Herstellung und deren Verwendung als Herbizide
DE2640730A1 (de)	1978-03-16	Heterocyclische phenylaether und diese enthaltende herbizide mittel
DD149013A5 (de)	1981-06-24	Herbizides und pflanzenregulierendes mittel
DE2744137C2 (de)	1984-05-10	N,N-Disubstituierte Benzolsulfonamid-Derivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende herbizide Zusammensetzung
DE2911865C2 (de)	1983-01-13	N-Halogenacetyl-phenylamino-carbonyl-oxime, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Mittel zur Bekämpfung von Unkraut
EP0036390B1 (de)	1983-10-26	Diphenyläther-Harnstoffe mit herbizider Wirkung
DE2637886C2 (sv)	1988-10-13
CH644096A5 (de)	1984-07-13	N-benzylhalogenacetamidderivate.
DE2524577C3 (de)	1980-05-22	Substituierte Tetrahydropyran-3,5dione und 13-Dioxan-4,6-dione, Verfahren zu ihrer Herstellung und ihre Verwendung als selektive Herbicide
EP0007089B1 (de)	1981-09-16	Acylanilide mit herbicider und fungicider Wirkung, Verfahren zu ihrer Herstellung und ihre Verwendung
DE3047629A1 (de)	1981-09-17	"tetrahydrofuranderivate"
DE2711928A1 (de)	1977-10-06	Acetanilidderivate, sie enthaltende herbizide mittel und ihre verwendung
DE3303388C2 (de)	1994-11-17	Chloracetamide, Verfahren zu ihrer Herstellung und diese enthaltende herbizide Mittel
EP0019762B1 (de)	1982-03-24	Triazolylderivate, Verfahren zu ihrer Herstellung sowie diese enthaltende Mittel zur Beeinflussung des Pflanzenwachstums
DE2826568A1 (de)	1979-01-04	Alpha -halogenacetamidderivate
DE3246705C2 (de)	1986-07-10	Tetrahydrobenzthiazolderivate und diese Verbindungen als wirksamen Bestandteil enthaltende herbizide Mittel
DD231978A5 (de)	1986-01-15	Herbizide zusammensetzung
EP0050097A1 (de)	1982-04-21	Neue alpha-(Pyridyl-2-oxy-phenoxy)-propionsäurederivate, Verfahren zu deren Herstellung, sowie deren Verwendung als Herbizide und/oder Pflanzenwachstumsregulatoren
DE3300056C2 (de)	1985-06-27	3-Nitrobenzolsulfonanilid-Derivate und diese enthaltende fungizide Mittel
DE2545964C2 (de)	1983-09-01	N-Halogenacetyl-N-aryl-glycinamide, Verfahren zu ihrer Herstellung sowie diese Verbindungen enthaltende herbizide Mittel
DE3237998A1 (de)	1983-05-05	Phenoxyalkylamidderivate, verfahren zu deren herstellung, herbizide zusammensetzungen, welche diese enthalten und deren verwendung zur bekaempfung von unkraut
DE3854436T2 (de)	1996-07-18	Alkoxymethylbenzoesäure.
DE2826531C2 (sv)	1988-04-14
DE2200325A1 (de)	1973-07-12	3-(2-phenylisopropyl)-harnstoffderivate
DE2154634A1 (sv)	1972-05-10

DE2711928A1 - Acetanilidderivate, sie enthaltende herbizide mittel und ihre verwendung - Google Patents

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Applications Claiming Priority (1)

Publications (1)

Family

ID=24683658

Family Applications (1)

Country Status (19)

Cited By (1)

Families Citing this family (2)

Family Cites Families (2)

Cited By (1)

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