KR890003669A - 제초 활성 페녹시알칸카복실산 유도체 - Google Patents

제초 활성 페녹시알칸카복실산 유도체 Download PDF

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KR890003669A
KR890003669A KR1019880010212A KR880010212A KR890003669A KR 890003669 A KR890003669 A KR 890003669A KR 1019880010212 A KR1019880010212 A KR 1019880010212A KR 880010212 A KR880010212 A KR 880010212A KR 890003669 A KR890003669 A KR 890003669A
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halogen
alkyl
compound
acid derivatives
herbicidal active
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KR1019880010212A
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KR960010789B1 (ko
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하루까즈 후가미
나오끼 히구찌
나오꼬 가와구찌
마사끼 하시모또
긴야 이데
도시오 다까하시
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사지 게이조오
산또리 가부시끼가이샤
요시토시 가즈오
시오노기 세이야꾸 가부시끼가이샤
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Priority claimed from JP19904187A external-priority patent/JPH0796543B2/ja
Priority claimed from JP19904087A external-priority patent/JP2507461B2/ja
Priority claimed from JP26656387A external-priority patent/JP2566991B2/ja
Priority claimed from JP1088A external-priority patent/JP2553122B2/ja
Application filed by 사지 게이조오, 산또리 가부시끼가이샤, 요시토시 가즈오, 시오노기 세이야꾸 가부시끼가이샤 filed Critical 사지 게이조오
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    • C07C69/675—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
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Abstract

내용 없음

Description

제초 활성 페녹시알칸카복실산 유도체
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (8)

  1. 하기 일반식(I)의 화합물 또는 이의 염.
    상기식에서, Q1는 CH 또는 N이고; R은 H 또는 C1-C4알킬이며; X는 H,할로겐 CF3또는 NO2이고; Y는 H 또는 할로겐이며; Z는 -O- 또는 -NH-이고; A는
    (여기에서, Q2및 13는 각각 CH 또는 N이고; R1및 R2는 각각 H,C1-C5알콕시, 또는 C2-C6알콕시 타보닐이며; R3,R4및 R5는 각각 H 또는 C1-C5알킬이고; R6는 H, 할로겐, 또는 C1-C5알킬이고; R11은 H ,C1-C5,C1-C5알콕시, C2-C6알케닐, C6-C10아릴, C7-C15아릴옥시알킬 또는 C7-C15아르알킬이며; R12및 R13은 각각 H 또는 C3-C4알킬렌을 형성하고; V1및 V2는 각각 H, 할로겐, NO2, CN, 또는 CF3이며; V3는 할로겐 또는 CF3이고; W1은 -O- 또는 -NH-이며; W2는 -(CH2)n-(여기에서, n은 0 또는 1이다. 또는 -CO-이고; X1은 할로겐이다)이다.
  2. 제 1항에 있어서, Q1이 CH 또는 N이고 R이 H 또는 C1-C5알킬이며; X가 H, 할로겐, CF3또는 NO2이고; Y가 H 또는 할로겐이며; Z가 -NH-이고; A가
    (여기에서, Q2는 CH 또는 N이고; V1및 V2는 각각 H, 할로겐, NO2, CH 또는 CF3이다)인 화합물.
  3. 제 1항에 있어서, Q1이 CH 또는 N이고; R이 H 또는 C1-C5알킬이며; X가 CF3또는 할로겐이고; Y가 H 또는 할로겐이고;Z가 -NH-이고; A가
    (여기에서, R1및 R2는 각각 H, C1-C5알킬, C1-C5알콕시 또는 C2-C5알콕시카보닐이다)인 화합물.
  4. 제 1항에 있어서, Q1이 CH 또는 N이고; R이 H 또는 C1-C5알킬이고; X가 CF3이고; 할로겐이며; Z가 -O- 또는 -NH-이고;
    A가(여기에서, R3,R4, 및 R5는 각각 H 또는 C1-C5알킬이고; R6는 H 또는 할로겐이며; X는 할로겐이다)인 화합물.
  5. 제 1항에 있어서, Q1이 N이고; R이 CH3이며; X가 CF3이고 Y가 H 또는 할로겐이며; Z가 -O-이고;
    A가(여기에서, R7,R8,R9및 R10은 각각 H 또는 C1-C5알킬이고; R11은 H 또는 C1-C5알킬이며; W1은 -O- 또는 -NH- 이고; W2는 -(CH2)n(여기에서, n은 0 또는 1이다), 또는 -CO-이다)인 화합물.
  6. 제 1항에있어서, Q1이 CH 또는 N이고; R이 H 또는 C1-C5알킬이며; X가 CF3이고; Y가 클로로이며; Z가 -O- 또는 -NH-이고; A가
    Q3는 CH 또는 N이고; V3는 CF3또는 할로겐이다)인 화합물.
  7. 제 1항에 있어서, Q1에이 N이고; R이 CH3이며; X가 CF3이고; Y가 H 또는 클로로이며; Z가 -O-이고;
    A가(여기에서, R12및 R13은 각각 H, C1-C5알킬이고; R14는 C1-C5알킬, C2-C6알케닐, C5-C10아릴 또는 C7-C10아르알킬이며; R13과 R14는 함께 C3-C4알킬렌을 형성한다)인 화합물.
  8. 활성성분으로서, 제 1항에 따른 화합물을 함유함을 특징으로 하는 제초제 조성물.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019880010212A 1987-08-11 1988-08-11 제초 활성 페녹시알칸카복실산 유도체 KR960010789B1 (ko)

Applications Claiming Priority (12)

Application Number Priority Date Filing Date Title
JP(?)62-199041 1987-08-11
JP62-199041 1987-08-11
JP19904187A JPH0796543B2 (ja) 1987-08-11 1987-08-11 アシルアミノベンゼンスルホンアミド誘導体及びそれを有効成分として含有する除草剤
JP(?)62-199040 1987-08-11
JP62-199040 1987-08-11
JP19904087A JP2507461B2 (ja) 1987-08-11 1987-08-11 α−フェノキシアルカンカルボン酸誘導体及びそれを有効成分として含有する除草剤
JP62-266563 1987-10-23
JP26656387A JP2566991B2 (ja) 1987-10-23 1987-10-23 α−ハロケトン誘導体、その製造法およびそれを有効成分として含有する除草剤
JP(?)62-266563 1987-10-23
JP63-000010 1988-01-04
JP1088A JP2553122B2 (ja) 1988-01-04 1988-01-04 α−置換ケトン誘導体またはその塩およびそれを含む除草剤
JP(?)63-000010 1988-01-04

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KR890003669A true KR890003669A (ko) 1989-04-17
KR960010789B1 KR960010789B1 (ko) 1996-08-08

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KR1019880010212A KR960010789B1 (ko) 1987-08-11 1988-08-11 제초 활성 페녹시알칸카복실산 유도체

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US (1) US4976773A (ko)
EP (1) EP0303415B1 (ko)
KR (1) KR960010789B1 (ko)
AR (1) AR243862A1 (ko)
AT (1) ATE114644T1 (ko)
AU (1) AU616676B2 (ko)
BR (1) BR8804062A (ko)
CA (1) CA1257598A (ko)
DE (1) DE3852235T2 (ko)
ES (1) ES2068830T3 (ko)
GR (1) GR3015185T3 (ko)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0580550T3 (da) * 1992-07-21 1998-02-02 Ciba Geigy Ag Oxamidsyrederivater som hypercholesterolæmiske midler
DE4323916A1 (de) * 1993-07-16 1995-01-19 Basf Ag Substituierte 2-Phenylpyridine
AU6829298A (en) 1997-03-20 1998-10-20 Basf Aktiengesellschaft Substituted 2-benz(o)ylpyridines, their preparation and their use as herbicides

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2617804C2 (de) * 1976-04-23 1985-01-24 Hoechst Ag, 6230 Frankfurt 2-(4-Phenoxy phenoxy)-propionsäurederivate und ihre Verwendung als Herbizide
DE2861073D1 (en) * 1977-06-29 1981-12-03 Ciba Geigy Ag Pyridyloxy-phenoxy-alkanoic acid derivatives , processes for their preparation and their use as herbicides or plant growth regulators
TR19824A (tr) * 1977-07-21 1980-01-24 Ishihara Sangyo Kaisha Trilorometilpiridoksifenoksipropionik as tuerevleri ve bunlari ihtiva eden herbisidler
DE2948095A1 (de) * 1979-11-29 1981-06-19 Hoechst Ag, 6230 Frankfurt Phenoxialkan- und phenoxialkencarbonsaeuren und deren derivate, ihre herstellung und verwendung
US4526608A (en) * 1982-07-14 1985-07-02 Zoecon Corporation Certain 2-pyridyloxyphenyl-oximino-ether-carboxylates, herbicidal compositions containing same and their herbicidal method of use
IL78554A0 (en) * 1985-05-02 1986-08-31 Dow Chemical Co Haloalkoxy anilide derivatives of 2-(4-heterocyclic oxyphenoxy-alkanoic acids and their use as herbicides

Also Published As

Publication number Publication date
EP0303415B1 (en) 1994-11-30
KR960010789B1 (ko) 1996-08-08
AR243862A1 (es) 1993-09-30
US4976773A (en) 1990-12-11
EP0303415A3 (en) 1989-12-20
GR3015185T3 (en) 1995-05-31
DE3852235T2 (de) 1995-04-06
EP0303415A2 (en) 1989-02-15
AU616676B2 (en) 1991-11-07
BR8804062A (pt) 1989-03-07
ES2068830T3 (es) 1995-05-01
ATE114644T1 (de) 1994-12-15
CA1257598A (en) 1989-07-18
AU2046988A (en) 1989-02-16
DE3852235D1 (de) 1995-01-12

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