KR880008747A - Herbicide composition - Google Patents

Herbicide composition Download PDF

Info

Publication number
KR880008747A
KR880008747A KR1019880000449A KR880000449A KR880008747A KR 880008747 A KR880008747 A KR 880008747A KR 1019880000449 A KR1019880000449 A KR 1019880000449A KR 880000449 A KR880000449 A KR 880000449A KR 880008747 A KR880008747 A KR 880008747A
Authority
KR
South Korea
Prior art keywords
dichlorophenoxy
herbicide composition
pentamethyleneurea
ethyl
general formula
Prior art date
Application number
KR1019880000449A
Other languages
Korean (ko)
Other versions
KR950009519B1 (en
Inventor
다쓰야 이께베
야스오 나까무라
겐지 모도지마
스스무 가또오
가쓰다다 야나기사와
Original Assignee
모찌즈끼 노부히꼬
구미아이 가가꾸 고오교오 가부시끼가이샤
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.)
Filing date
Publication date
Priority claimed from JP62012065A external-priority patent/JPS63179806A/en
Priority claimed from JP62012066A external-priority patent/JPH0193503A/en
Application filed by 모찌즈끼 노부히꼬, 구미아이 가가꾸 고오교오 가부시끼가이샤 filed Critical 모찌즈끼 노부히꼬
Publication of KR880008747A publication Critical patent/KR880008747A/en
Application granted granted Critical
Publication of KR950009519B1 publication Critical patent/KR950009519B1/en

Links

Classifications

    • 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/38Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof

Landscapes

  • 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)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

내용 없음.No content.

Description

제초제 조성물Herbicide composition

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음As this is a public information case, the full text was not included.

Claims (9)

일반식(Ⅰ) :General formula (Ⅰ): (식중, X는 저급알킬기를 표시하며, n은 0내지 2의 정수를 표시하며, m은 4 내지 6의 정수를 표시한다.)로 표시되는 치환페녹시효소와, 메틸 2-[(4,6-디메톡시피리미딘-2-일)카르바모일술파밀메틸] 벤조에이트, 에틸 5-[(4,6-디메톡시피리미딘-2-일)카르바모일술파밀메틸]-1-메틸 피라졸-4-카르바복실레이트 및 3-(2-페닐이소프로필)-1-(피라톨릴)요소로 이루어진 군에서 선택된 제2의 화합물을 유효성분으로서 함유하는 것을 특징으로 하는 제초제 조성물.(Wherein X represents a lower alkyl group, n represents an integer of 0 to 2, m represents an integer of 4 to 6), and methyl 2-[(4, 6-dimethoxypyrimidin-2-yl) carbamoylsulfamilmethyl] benzoate, ethyl 5-[(4,6-dimethoxypyrimidin-2-yl) carbamoylsulfylmethyl] -1 -Herbicide composition characterized in that it contains a second compound selected from the group consisting of -methyl pyrazole-4-carbacarboxylate and 3- (2-phenylisopropyl) -1- (pyratolyl) urea as an active ingredient. . 제1항에 있어서, 일반식(Ⅰ)의 치환 페녹시효소가 3-(3,5-디클로로페녹시)-1,1-테트라메틸렌요소,3-(3,5-디클로로페녹시)-1,1-펜타메틸렌요소, 3-(3,5-디클로로페녹시)-1,1-(1-메틸)-펜타메틸렌요소, 3-(3,5-디클로로페녹시)-1,1-(1-에틸)-펜타메틸렌요소, 3-(3,5-디클로로페녹시)-1,1-(2, 4-디메틸)-펜타메틸렌요소, 3 및 -(3,5-디클로로페녹시)-1,1-(2,4-디메틸)-펜타메틸렌요소 3-및-(3,5-디클로로페녹시)-1,-헥사메틸렌요소로부터 선택된 1종 이상의 것을 특징으로 하는 제초제 조성물.The method of claim 1, wherein the substituted phenoxyase of formula (I) is 3- (3,5-dichlorophenoxy) -1,1-tetramethyleneurea, 3- (3,5-dichlorophenoxy) -1 , 1-pentamethyleneurea, 3- (3,5-dichlorophenoxy) -1,1- (1-methyl) -pentamethyleneurea, 3- (3,5-dichlorophenoxy) -1,1- ( 1-ethyl) -pentamethyleneurea, 3- (3,5-dichlorophenoxy) -1,1- (2,4-dimethyl) -pentamethyleneurea, 3 and-(3,5-dichlorophenoxy)- A herbicide composition characterized by at least one member selected from 1,1- (2,4-dimethyl) -pentamethyleneurea 3-and- (3,5-dichlorophenoxy) -1, -hexamethyleneurea. 제2항에 있어서, 일반식(Ⅰ)의 치환페녹시효소가 3-(3,5-디클로로페녹시) -1,1-(1-에틸)-펜타메틸렌요소인 것을 특징으로 하는 제초제 조성물.3. The herbicide composition according to claim 2, wherein the substituted phenoxyase of the general formula (I) is 3- (3,5-dichlorophenoxy) -1,1- (1-ethyl) -pentamethyleneurea. 제1 또는 제2에 있어서, 제2의 화합물이 메틸 2-[(4,6-디메톡시 피리미딘-2-일)카르바모일술파밀메틸]벤조에이트인 것을 특징으로 하는 제초제 조성물.The herbicidal composition according to claim 1 or 2, wherein the second compound is methyl 2-[(4,6-dimethoxy pyrimidin-2-yl) carbamoylsulfamilmethyl] benzoate. 제1항 또는 제2항에 있어서, 제2의 화합물이 에틸 5-[(4,6-디메톡시 피리미딘-2-일)카르바모일술파밀]-1-메틸피라졸-4-카르복실레이트인 것을 특징으로 하는 제초제 조성물.3. The compound of claim 1, wherein the second compound is ethyl 5-[(4,6-dimethoxy pyrimidin-2-yl) carbamoylsulfamil] -1-methylpyrazole-4-carboxyl It is a rate, The herbicide composition characterized by the above-mentioned. 제3항에 있어서, 제2의 화합물이 3-(2-페닐이소프로필)-1-(피라톨릴) 요소인 것을 특징으로 하는 제초제 조성물.4. The herbicide composition according to claim 3, wherein the second compound is 3- (2-phenylisopropyl) -1- (pyratolyl) urea. 제4항에 있어서, 일반식(Ⅰ)의 치환페녹시요소와, 메틸 2-[(4,6-디메톡시피리딘-2-일)카르바모일술파밀메틸]벤조에이트의 배출비가 중량비로 1 : 0.01∼1부인 것을 특징으로 하는 제초제 조성물.The discharging ratio of the substituted phenoxyurea of the general formula (I) and methyl 2-[(4,6-dimethoxypyridin-2-yl) carbamoylsulfylmethyl] benzoate according to claim 4, wherein : 0.01-1 part, The herbicide composition characterized by the above-mentioned. 제5항에 있어서, 일반식(Ⅰ)의 치환페녹시요소와, 에틸 2-[(4,6-디메톡시피리딘-2일)카르바모일술파밀메틸]-1-메틸피라졸-4-카르복실레이트의 배합비가 중량비로 1 : 0.01∼1부인 것을 특징으로 하는 제초제 조성물.The substituted phenoxyurea of the general formula (I) and ethyl 2-[(4,6-dimethoxypyridin-2yl) carbamoylsulfamilmethyl] -1-methylpyrazole-4- The compounding ratio of carboxylate is 1: 0.01-1 part by weight ratio, The herbicide composition characterized by the above-mentioned. 제6항에 있어서, 일반식(Ⅰ)의 치환페녹시요소와, 에틸 3-(2-페닐이소프로필)-1-(피라톨릴)요소와 배합비율이 중량비로 1 : 0.01∼10부인 것을 특징으로 하는 제초제 조성물.7. The substituted phenoxy urea of the general formula (I), ethyl 3- (2-phenylisopropyl) -1- (pyratolyl) urea and the blending ratio of 1 to 0.01 to 10 parts by weight ratio according to claim 6, Herbicide composition ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019880000449A 1987-01-21 1988-01-21 Herbicide compositions KR950009519B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP62012065A JPS63179806A (en) 1987-01-21 1987-01-21 Herbicide composition
JP62012066A JPH0193503A (en) 1987-01-21 1987-01-21 Herbicidal composition
JP62-12066 1987-01-21
JP62-12065 1987-01-21

Publications (2)

Publication Number Publication Date
KR880008747A true KR880008747A (en) 1988-09-13
KR950009519B1 KR950009519B1 (en) 1995-08-23

Family

ID=26347613

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019880000449A KR950009519B1 (en) 1987-01-21 1988-01-21 Herbicide compositions

Country Status (1)

Country Link
KR (1) KR950009519B1 (en)

Also Published As

Publication number Publication date
KR950009519B1 (en) 1995-08-23

Similar Documents

Publication Publication Date Title
KR970014565A (en) Granular herbicidal composition
KR910016742A (en) Alkylated oxo-piperazinyl-triazine
KR900014370A (en) Trifluoromethylphenylrazolylmethyloxyran. Its preparation and its use as crop protection agents
KR870007876A (en) N&#39;-substituted-N-acyl-N&#39;-alkylcarbonylhydrazine compound having an insecticidal effect
KR910002800A (en) 4-acyloxyquinoline derivatives and pesticidal or acaricide compositions containing them
BR9608568B1 (en) biocidal composition stabilized against degradation of the halopropargyl active compound.
KR920006348A (en) Picoline oxide and preparation method thereof
KR870011093A (en) N-cyanoalkylisonicotinamide derivatives
KR880008747A (en) Herbicide composition
KR880001618A (en) How to fight diseases caused by fungi on plants
KR927003553A (en) Alalkyloxyamine Derivatives and Herbicide Compositions
KR830006895A (en) Process for preparing thiocarbamate compound
KR900013853A (en) Antifouling Agents for Fishing Nets
KR910016252A (en) Insecticides and Fungicides
KR880006983A (en) Seed disinfectant
KR960000869A (en) Isothiazole derivatives and uses thereof
KR930004273A (en) Benzoyl urea derivatives containing pyrazole
KR900009600A (en) Pyrazole Compounds, Preparations and Uses thereof
KR900004696A (en) Naphthidazole-4-9-quinone and their use to modulate weed growth
KR930701108A (en) Herbicide composition for use in paddy fields
KR890009270A (en) Plant protection fungicides
KR860002961A (en) Herbicidal composition
KR890009887A (en) Imidazole derivatives
KR830001275A (en) Pyrazolyl pyrimidine derivatives and fungicides for agricultural and horticultural use
KR920021568A (en) Novel 1,2,4-triazole derivatives with bactericidal action

Legal Events

Date Code Title Description
A201 Request for examination
G160 Decision to publish patent application
E701 Decision to grant or registration of patent right
NORF Unpaid initial registration fee