KR870006028A - 에폭사이드 제초제 - Google Patents
에폭사이드 제초제 Download PDFInfo
- Publication number
- KR870006028A KR870006028A KR860010248A KR860010248A KR870006028A KR 870006028 A KR870006028 A KR 870006028A KR 860010248 A KR860010248 A KR 860010248A KR 860010248 A KR860010248 A KR 860010248A KR 870006028 A KR870006028 A KR 870006028A
- Authority
- KR
- South Korea
- Prior art keywords
- composition according
- active ingredient
- phenyloxirane
- independently
- chlorobenzoyl
- Prior art date
Links
- 150000002118 epoxides Chemical class 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims 18
- 239000004480 active ingredient Substances 0.000 claims 12
- AUYKOKZTVPQSFU-UHFFFAOYSA-N phenyl-(2-phenyloxiran-2-yl)methanone Chemical compound C1OC1(C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 AUYKOKZTVPQSFU-UHFFFAOYSA-N 0.000 claims 5
- 241000196324 Embryophyta Species 0.000 claims 4
- 241000209094 Oryza Species 0.000 claims 4
- 235000007164 Oryza sativa Nutrition 0.000 claims 4
- 244000038559 crop plants Species 0.000 claims 4
- 235000009566 rice Nutrition 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- IFQFHKMOAIYTMC-UHFFFAOYSA-N 2-benzyl-2-phenyloxirane Chemical compound C1OC1(C=1C=CC=CC=1)CC1=CC=CC=C1 IFQFHKMOAIYTMC-UHFFFAOYSA-N 0.000 claims 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 230000035784 germination Effects 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 230000008635 plant growth Effects 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- DEFCCERBQIEZET-UHFFFAOYSA-N (2-chlorophenyl)-(2-phenyloxiran-2-yl)methanone Chemical compound ClC1=CC=CC=C1C(=O)C1(C=2C=CC=CC=2)OC1 DEFCCERBQIEZET-UHFFFAOYSA-N 0.000 claims 1
- BMXDHHJCRSTMIH-UHFFFAOYSA-N (4-chlorophenyl)-(2-phenyloxiran-2-yl)methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1(C=2C=CC=CC=2)OC1 BMXDHHJCRSTMIH-UHFFFAOYSA-N 0.000 claims 1
- GSWXGGAXHUUVHY-UHFFFAOYSA-N (4-chlorophenyl)-[2-(2-chlorophenyl)oxiran-2-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1(C=2C(=CC=CC=2)Cl)OC1 GSWXGGAXHUUVHY-UHFFFAOYSA-N 0.000 claims 1
- FKZPHOULEFFRRD-UHFFFAOYSA-N (4-chlorophenyl)-[2-(3-chlorophenyl)oxiran-2-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1(C=2C=C(Cl)C=CC=2)OC1 FKZPHOULEFFRRD-UHFFFAOYSA-N 0.000 claims 1
- LLNPOWBZRKKZOT-UHFFFAOYSA-N (4-chlorophenyl)-[2-(3-methoxyphenyl)oxiran-2-yl]methanone Chemical compound COC1=CC=CC(C2(OC2)C(=O)C=2C=CC(Cl)=CC=2)=C1 LLNPOWBZRKKZOT-UHFFFAOYSA-N 0.000 claims 1
- BQXGTSYBOZWLRK-UHFFFAOYSA-N (4-chlorophenyl)-[2-(4-chlorophenyl)oxiran-2-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1(C=2C=CC(Cl)=CC=2)OC1 BQXGTSYBOZWLRK-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- KLCWRYSESIMCDF-UHFFFAOYSA-N [2-(3-bromophenyl)oxiran-2-yl]-(4-chlorophenyl)methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1(C=2C=C(Br)C=CC=2)OC1 KLCWRYSESIMCDF-UHFFFAOYSA-N 0.000 claims 1
- KREZIMIXJUUALV-UHFFFAOYSA-N [2-(3-methylphenyl)oxiran-2-yl]-phenylmethanone Chemical compound CC1=CC=CC(C2(OC2)C(=O)C=2C=CC=CC=2)=C1 KREZIMIXJUUALV-UHFFFAOYSA-N 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 239000005648 plant growth regulator Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/12—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with hydrogen peroxide or inorganic peroxides or peracids
-
- 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
- A01N43/04—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 one hetero atom
- A01N43/20—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 one hetero atom three- or four-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/32—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by aldehydo- or ketonic radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Inorganic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Epoxy Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (22)
- 불활성 보조제와 함께 활성성분으로서 일반식(I)의 2-벤조일-2-페닐옥시란을 라세미체 또는 광학활성 에난티오머 형태로 함유하는 제조제 및 식물생장 조절제 조성물:여기서, m 및 n은 각각 독립적으로 0,1,2 또는 3이고; R 및 R′은 각각 독립적으로 할로겐 원자, C1-C4알킬, C1-C4알콕시,C1-C4할로알킬 또는 C1-C4할로 알콕시기 이거나;또는 니트로 또는 시아노기; 또는(R)m에 의해 치환된 페녹시기임.
- 제1항에 있어서, m 및 n이 각각 독립적으로 0,1,2 또는 3이고;R 및 R′이 각각 독립적으로 플루오르, 염소, 브롬, 메틸, 메톡시 또는 트리플루오로메틸이거나; 또는 R이 또한 (R)m에 의해 치환된 페녹시기인 제1항에 따르는 일반식(I)의 2-벤질-2-페닐옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, m 및 n이 각각 독립적으로 0,1,2 또는 3이고;R 및 R′이 각각 독립적으로 플루오르, 염소, 메틸, 메톡시 또는 트리플루오르메틸인 제1항에 따르는 일반식(I)의 2-벤질-2-페닐옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-벤조일-2-페닐옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-(4-브로모벤조일-2-페닐)옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-(4-클로로벤조일)-2-(4-클로로페닐)옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-(4-클로로벤조일-2-(2-클로로페닐)옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-벤조일-2-m-톨릴옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-(2-클로로벤조일)-2-페닐옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-(4-클로로벤조일)-2-(3-클로로페닐)옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-(4-클로로벤조일)-2-(3-브로모페닐)옥시란을 활성성분으로서 함유하는 조성물.
- 제1항에 있어서, 2-(4-클로로벤조일)-2-페닐옥시란을 활성성분으로서 함유하는 조성물.
- 유용식물 또는 농경지에 제1항에 따르는 조성물을 제초 유효량으로 투여하여, 유용식물의 농지물에서 발아전 또는 발아 후에 잡초를 선택적으로 방제하는 방법.
- 제13항에 있어서, 벼 작물을 발아전 또는 발아후에 제초 유효량의 제1항에 따르는 조성물로 처리하여 벼 작물에서 잡초를 선택적으로 방제하는 방법.
- 제13항에 있어서, 벼, 그것의 농경지 또는 그것의 종자를 유효량의 제1항에 따르는 조성물로 처리하는 방법.
- 제13항에 있어서, 유용식물 또는 그것의 농경지를 제초 유효량의 제1항에 따르는 조성물로 처리하여, 유용식물의 농작물에서 유해한 잡초를 방제하는 방법.
- 제13항에 있어서, 식물의 생장기간동안 유효량의 제1항에 따르는 조성물로 식물을 처리하여, 2배엽 단계 이상에서 식물의 생장을 억제하는 방법.
- 유효량의 제1항에 따르는 조성물로 처리한 벼의 종자.
- 하기 일반식(I*)의 벤조일-2-페닐옥시란의 광학 활성 에난티오머;여기에서, m 및 n은 각각 독립적으로 0,1,2 또는 3이고; R 및 R′은 각각 독립적으로 할로겐원자, C1-C4알킬, C1-C4알콕시, C1-C4할로알킬 또는 C1-C4할로알콕시기 이거나;또는 니트로 또는 시아노기;(R)m에 의해 치환된 페녹시기임.
- 라세미체 또는 광학활성 에난티오머 형태의 하기일반식(Ia)의 2-벤조일-2-페닐옥시란;여기서, R은 할로겐, C1-C4알킬 또는 C1-C4알콕시이고; R″은 R에 대한 의미중 하나이거나 또는 수소이며; X′및 n은 제1항에서 정의한 바와 같음.
- 제20항에 있어서, R″이 수소인 2-벤조일-2-페닐옥시란.
- 제20항에 있어서, 2-(4-클로로벤조일)-2-(3-메톡시페닐)옥시란.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH0511/85-3 | 1985-12-02 | ||
CH513185 | 1985-12-02 | ||
CH5131/85-3 | 1985-12-02 | ||
CH2617/86-0 | 1986-06-30 | ||
CH261786 | 1986-06-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR870006028A true KR870006028A (ko) | 1987-07-08 |
KR920001304B1 KR920001304B1 (ko) | 1992-02-10 |
Family
ID=25690956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019860010248A KR920001304B1 (ko) | 1985-12-02 | 1986-12-02 | 에폭사이드 제초제 |
Country Status (6)
Country | Link |
---|---|
US (2) | US4849007A (ko) |
EP (1) | EP0225290B1 (ko) |
KR (1) | KR920001304B1 (ko) |
BR (1) | BR8605859A (ko) |
DE (1) | DE3667011D1 (ko) |
PH (1) | PH22669A (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100415595B1 (ko) * | 1995-07-25 | 2004-05-12 | 가부시키가이샤 에스디에스 바이오테크 | 수전용제초제조성물 |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4975459A (en) * | 1989-12-13 | 1990-12-04 | Rohm And Haas Company | Microbicidal and plant growth regulating compounds |
EP0641515A1 (en) * | 1993-08-11 | 1995-03-08 | Shell Internationale Researchmaatschappij B.V. | Herbicidal methods and compositions |
JP2636819B2 (ja) * | 1994-12-20 | 1997-07-30 | 日本たばこ産業株式会社 | オキサゾール系複素環式芳香族化合物 |
EP2654433B1 (en) | 2010-12-21 | 2017-08-30 | Bayer Cropscience LP | Sandpaper mutants of bacillus and methods of their use to enhance plant growth, promote plant health and control diseases and pests |
BR112014005654A2 (pt) | 2011-09-12 | 2017-03-28 | Bayer Cropscience Lp | métodos para melhorar a saúde e promover o crescimento de uma planta e/ou de melhorar o amadurecimento da fruta |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3501503A (en) * | 1967-09-12 | 1970-03-17 | Merck & Co Inc | (4-(2,3-epoxyalkanoyl)phenoxy)acetic acids |
US3930835A (en) * | 1970-08-06 | 1976-01-06 | The Dow Chemical Company | Pesticidal compositions and methods employing substituted oxirane compounds |
US3719465A (en) * | 1970-08-06 | 1973-03-06 | Dow Chemical Co | Composition and method for controlling undesirable plant growth |
NL7505160A (nl) * | 1972-10-02 | 1976-11-03 | Dow Chemical Co | Werkwijze voor het bereiden van een herbicide. |
US3933472A (en) * | 1972-02-29 | 1976-01-20 | Buckman Laboratories, Inc. | Substituted alkylaryl ketones and methods of use as herbicides |
US4211549A (en) * | 1975-12-08 | 1980-07-08 | The Dow Chemical Company | Substituted oxirane compounds |
US4490165A (en) * | 1980-05-23 | 1984-12-25 | American Cyanamid Company | Meta-(phenylalkoxy)phenyl-N-methoxy-N-methylurea compounds, methods for preparing same and herbicidal use thereof |
PH19709A (en) * | 1982-11-23 | 1986-06-16 | Ciba Geigy Ag | Microbicidal 1-carbonyl-1-phenoxyphenyl-2-azolylethanol derivatives |
EP0117578A3 (en) * | 1983-02-23 | 1985-01-30 | Shionogi & Co., Ltd. | Azole-substituted alcohol derivatives |
DE3335477A1 (de) * | 1983-09-30 | 1985-04-18 | Bayer Ag, 5090 Leverkusen | 2-aryl-2-halogenalkyl-oxirane |
-
1986
- 1986-11-24 US US06/934,298 patent/US4849007A/en not_active Expired - Fee Related
- 1986-11-26 DE DE8686810546T patent/DE3667011D1/de not_active Expired
- 1986-11-26 EP EP86810546A patent/EP0225290B1/de not_active Expired
- 1986-12-01 BR BR8605859A patent/BR8605859A/pt unknown
- 1986-12-02 KR KR1019860010248A patent/KR920001304B1/ko active IP Right Grant
- 1986-12-02 PH PH34539A patent/PH22669A/en unknown
-
1988
- 1988-02-29 US US07/161,812 patent/US4894083A/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100415595B1 (ko) * | 1995-07-25 | 2004-05-12 | 가부시키가이샤 에스디에스 바이오테크 | 수전용제초제조성물 |
Also Published As
Publication number | Publication date |
---|---|
EP0225290A1 (de) | 1987-06-10 |
US4849007A (en) | 1989-07-18 |
PH22669A (en) | 1988-11-14 |
BR8605859A (pt) | 1987-08-25 |
DE3667011D1 (en) | 1989-12-28 |
EP0225290B1 (de) | 1989-11-23 |
KR920001304B1 (ko) | 1992-02-10 |
US4894083A (en) | 1990-01-16 |
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