KR930000013A - Herbicide composition - Google Patents

Herbicide composition Download PDF

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Publication number
KR930000013A
KR930000013A KR1019920009801A KR920009801A KR930000013A KR 930000013 A KR930000013 A KR 930000013A KR 1019920009801 A KR1019920009801 A KR 1019920009801A KR 920009801 A KR920009801 A KR 920009801A KR 930000013 A KR930000013 A KR 930000013A
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South Korea
Prior art keywords
formula
weight ratio
oxiacetamide
composition
yloxy
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KR1019920009801A
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Korean (ko)
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도시오 고또
히데노리 하야가와
히로시 미유끼
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다떼노 고이찌
니혼 바이엘 아그로켐 케이.케이.
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Publication of KR930000013A publication Critical patent/KR930000013A/en

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/18Biocides, 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

Abstract

내용 없음No content

Description

제초제 조성물Herbicide composition

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (13)

일반식(I)의 옥시아세트아미드, 및 술폰아미드, 피라졸, 프로피온 아닐리드, 트리아진, 카바메이트, 디페닐에테르및 산 아미드로 이루어진 그룹으로부터 선택된 적어도 하나의 제초 활성 물질을 함유하는 조성물의 제초 유효량을 함유함을 특징으로 하는 제초제 조성물.Herbicidally effective amount of a composition containing oxiacetamide of formula (I) and at least one herbicidally active substance selected from the group consisting of sulfonamides, pyrazoles, propion anilides, triazines, carbamates, diphenylethers and acid amides Herbicide composition characterized in that it contains. 상기 식에서 R1은 할로겐 또는 시아노이며, R2는 할로겐이거나, R1및 R2가 이들이 결합된 헤테로 환과 함께는, 할로겐에 의해 치환될 수 있는 벤조-융합 환을 형성할 수 있으며, R3는 C1-4알킬이며, X는 산소 또는 황이고, Y는 C1-4알킬이며, n은 0 또는 1이다.Wherein R 1 is halogen or cyano, R 2 is halogen, or R 1 and R 2 together with the hetero ring to which they are attached may form a benzo-fused ring which may be substituted by halogen, R 3 Is C 1-4 alkyl, X is oxygen or sulfur, Y is C 1-4 alkyl and n is 0 or 1. 제1항에 있어서, 술폰아미드에 대한 일반식(I)의 옥시아세트아미드의 중량비가 1:0.01내지 1:2이고, 피라졸에 대한 일반식 (I)의 옥시아시트아미드의 중량비가 1:2.5내지 1:35이고, 프로피온아닐리드에 대한 일반식 (I)의 옥시아세트아미드의 중량비가 1:0.6내지 1:50이며, 트리아진에 대한 일반식 (I)의 옥시아세트아미드의 중량비가 1:0.06내지 1:10이고, 카바메이트에 대한 일반식(I)의 옥시아세트아미드의 중량비가 1:3내지 1:15이며, 디페닐에테르에 대한 일반식(I)의 옥시아세트아미드의 중량비가 1:5내지 1:35이고, 산아미드에 대한 일반식 (I)의 옥시아세트아미드의 중량비가 1:3.5내지 1:25인 조성물.The weight ratio of oxiacetamide of formula (I) to sulfonamide is from 1: 0.01 to 1: 2, and the weight ratio of oxiacitamide of formula (I) to pyrazole is 1: 2.5 to 1:35, the weight ratio of oxiacetamide of formula (I) to propionanilide is from 1: 0.6 to 1:50, and the weight ratio of oxiacetamide of general formula (I) to triazine is 1: 0.06 to 1:10, the weight ratio of oxiacetamide of formula (I) to carbamate is 1: 3 to 1:15, and the weight ratio of oxyacetamide of general formula (I) to diphenylether is 1 A composition wherein the weight ratio of oxiacetamide of formula (I) to acid amide is from 1: 3.5 to 1:25. 제1항에 있어서, 일반식 (I)의 옥시아세트아미드에시 R1이 염소 또는 시아노를 나타내며, R2는 염소를 나타내거나, R1및 R2가 이들이 결합된 헤테로 환과 함께는, 염소-치환된 벤조-융합 환을 형성할 수 있으며, R3는 메틸 또는 이소프로필을 나타내고, X는 산소 또는 황을 나타내며, Y는 메틸을 나타내고, n이 0 또는 1을 나타내는 조성물.The oxyacetamide of formula (I) wherein R 1 represents chlorine or cyano, R 2 represents chlorine, or R 1 and R 2 together with the heterocycle to which they are attached, chlorine A substituted benzo-fusion ring, wherein R 3 represents methyl or isopropyl, X represents oxygen or sulfur, Y represents methyl and n represents 0 or 1. 제1항에 있어서. 옥시아세트아미드가, 4,5-디클로로티아졸-2-일옥시-N-메틸아세트아닐리드, 6-클로로벤즈옥사졸-2-일옥-N-메틸아세트(2-메틸아닐리드), 6-클로로벤즈옥사졸-2-일옥-N-메틸아세트(3-메틸아닐리드), 5-클로로-4-시아노티아졸-2-일옥시-N-메틸세트아닐리드, 6-클로로벤즈옥사졸-2-일옥시-N-이소프로필아세트 (3-메틸아닐리드 또는 7-클로로벤조티아졸-2-일옥시-N-메틸아세트아닐리드인 조상들.The method of claim 1. Oxyacetamide, 4,5-dichlorothiazol-2-yloxy-N-methylacetanilide, 6-chlorobenzoxazol-2-ylox-N-methylacetide (2-methylanilide), 6-chlorobenz Oxazol-2-ylox-N-methylacetide (3-methylanilide), 5-chloro-4-cyanothiazol-2-yloxy-N-methylcetanilide, 6-chlorobenzoxazol-2-yloxy Ancestors which are -N-isopropylacet (3-methylanilide or 7-chlorobenzothiazol-2-yloxy-N-methylacetanilide). 제1항에 있어서, 술폰아미드가 N-2-비페닐릴술포 N'-(4,6-디메톡시-1,3,5-트리아진-2-일)우레아, 에틸 5-[3-(4,6-디메톡시피리미딘-2-일)우레이도술포닐)-1-메틸피라졸-4-카복실레이트, 메틸2-[3-(4,6-디메톡시피리미딘-2-일)우레이도술포닐메틸]벤조에이트, 3-(4,6-디메톡시-1,3,5-트리아진-2-일)-1-[2-(2-메톡시에톡시)페닐술포닐)우레아, N-(2-클로로이미다졸[1,2-a]피리딘-3-일-술포닐)-N'-(4,6-디메톡시피리미디닐)우레아, 또는N'-(4,6-디메톡시피리미딘-2-일)-N"-(4-메틸페닐술포닐아미노)-N"-(4-에톡시카보닐-1-메틸피라졸-5-일-술포닐)구아니딘인 조상들.The compound of claim 1, wherein the sulfonamide is N-2-biphenylylsulfo N '-(4,6-dimethoxy-1,3,5-triazin-2-yl) urea, ethyl 5- [3- ( 4,6-dimethoxypyrimidin-2-yl) ureidosulfonyl) -1-methylpyrazole-4-carboxylate, methyl2- [3- (4,6-dimethoxypyrimidin-2-yl ) Ureidosulfonylmethyl] benzoate, 3- (4,6-dimethoxy-1,3,5-triazin-2-yl) -1- [2- (2-methoxyethoxy) phenylsulfonyl) Urea, N- (2-chloroimidazole [1,2-a] pyridin-3-yl-sulfonyl) -N '-(4,6-dimethoxypyrimidinyl) urea, or N'-(4, 6-dimethoxypyrimidin-2-yl) -N "-(4-methylphenylsulfonylamino) -N"-(4-ethoxycarbonyl-1-methylpyrazol-5-yl-sulfonyl) guanidine Ancestors. 제1항에 있어서, 피라졸이 4-(2,4-디클로로벤조일)-1,3-디메틸피라졸-5-일-p-톨루엔술포네이트, 2-[4-(2,4-디클로로벤조일)-1,3-디메털피라졸-5-일)아세토페는, 또는 2-[4-(2,4-디클로로-m-톨루오일)-1,3-디메틸피라졸-5-일옥시)-4-메틸아세토페논인 조성물.The compound of claim 1, wherein the pyrazole is 4- (2,4-dichlorobenzoyl) -1,3-dimethylpyrazol-5-yl-p-toluenesulfonate, 2- [4- (2,4-dichlorobenzoyl ) -1,3-dimetalpyrazol-5-yl) acetope or 2- [4- (2,4-dichloro-m-toluoyl) -1,3-dimethylpyrazol-5-yloxy ) -4-methylacetophenone. 제1항에 있어서, 프로피온아닐리드가 2-(?-나프틸옥시)프로피온아닐리드, 또는 (RS)-2-(2,4-디클로로-m-톨릴옥시)프로피온아닐리드인 조성물.The composition of claim 1 wherein propionanilide is 2-(?-Naphthyloxy) propionanilide or (RS) -2- (2,4-dichloro-m-tolyloxy) propionanilide. 제1항에 있어서 트리아진이 2,4-비스(에틸아미노)-6-(메틸아미노)-1,3,5-트리아진, 또는 2-에틸아미노-4-(1,2-디에틸프로필아미노)-6-메틸티오-1,3,5-트리아진인 조성물.The compound according to claim 1, wherein the triazine is 2,4-bis (ethylamino) -6- (methylamino) -1,3,5-triazine, or 2-ethylamino-4- (1,2-diethylpropylamino ) -6-methylthio-1,3,5-triazine. 제1항에 있어서, 카바메이트가S-p-클로로벤질 디에틸티오카바메이트, S-l-메틸-1-페닐에털 피페리딘-1-카보티오에이트, 또는 S-벤질 1,2-디메틸프로필(에틸)티오카바메이트인 조성물.The method of claim 1 wherein the carbamate is Sp-chlorobenzyl diethylthiocarbamate, Sl-methyl-1-phenylether piperidine-1-carbothioate, or S-benzyl 1,2-dimethylpropyl (ethyl ) Thiocarbamate. 제1항에 있어서, 디페닐에테르가 2,4,6-트리클로로페닐-4'-니트로페닐에테르, 또는2,4-디클로로페닐-3'-메톡시-4'-니트로페닐에테르인 조성물.The composition according to claim 1, wherein the diphenyl ether is 2,4,6-trichlorophenyl-4'-nitrophenylether or 2,4-dichlorophenyl-3'-methoxy-4'-nitrophenylether. 제1항에 있어서, 산 아미드가 (RS)-2-브로모-N-(α,α-디메틸벤질)-3,3-디메틸부틸아미드인 조성물.The composition of claim 1 wherein the acid amide is (RS) -2-bromo-N- (α, α-dimethylbenzyl) -3,3-dimethylbutylamide. 제1항에 따르는 조성물이 제초 유효량을 잡초 또는 잡초서식지에 적용시킴에 특징으로 하여 잡초를 방제하는 방법.A method according to claim 1, wherein the composition according to claim 1 is applied to the weed or weed habitat. 제2항에 따르는 조성물의 제초 유효량을 잡초 또는 잡초서식지에 적용시킴에 특징으로 하여 잡초를 방제하는 방법.A method for controlling weeds, characterized in that the herbicidally effective amount of the composition according to claim 2 is applied to weeds or weed habitats. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019920009801A 1991-06-10 1992-06-05 Herbicide composition KR930000013A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP163438/91 1991-06-10
JP16343891 1991-06-10
JP3299558A JPH0551304A (en) 1991-06-10 1991-10-21 Herbicide composition
JP299558/91 1991-10-21

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KR930000013A true KR930000013A (en) 1993-01-15

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CN (1) CN1068013A (en)
TW (1) TW217981B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2753368B1 (en) 1996-09-13 1999-01-08 Chauvin Jean Luc EXPANSIONAL OSTEOSYNTHESIS CAGE
JP3743602B2 (en) 1998-05-25 2006-02-08 株式会社タニタ Body fat scale with height measuring device
SK285058B6 (en) * 1998-06-16 2006-05-04 Basf Aktiengesellschaft Herbicidal mixtures having a synergistic effect, herbicidal composition containing them, method for their producing and use thereof
KR100352942B1 (en) * 1999-09-08 2002-09-16 한국화학연구원 Fluorinated vinyloxyacetamide derivatives having sulfide or sulfonyl substituent, process for preparing same and herbicidal composition comprising same
TW201245155A (en) 2010-09-01 2012-11-16 Du Pont Fungicidal pyrazoles
WO2015187937A1 (en) 2014-06-04 2015-12-10 Wenzel Spine, Inc. Bilaterally expanding intervertebral body fusion device

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CN1068013A (en) 1993-01-20
TW217981B (en) 1993-12-21
JPH0551304A (en) 1993-03-02

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