KR960040155A - 방오제로서 피롤 화합물의 용도 - Google Patents
방오제로서 피롤 화합물의 용도 Download PDFInfo
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- KR960040155A KR960040155A KR1019960017418A KR19960017418A KR960040155A KR 960040155 A KR960040155 A KR 960040155A KR 1019960017418 A KR1019960017418 A KR 1019960017418A KR 19960017418 A KR19960017418 A KR 19960017418A KR 960040155 A KR960040155 A KR 960040155A
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
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Abstract
본원에서는 부착성 생물과 방오-효과량의 2-아릴피롤 화합물을 접촉시키는 것으로 특징지워지는 수중 표면에 대한 부착성 생물의 부착을 구제 또는 퇴치하는 방법을 제공한다. 해수 및 담수 부탁성 생물에 의한 오염으로부터 수중 구조물을 보호하는 방법 이를 위한 방오 조성물 또한 제공된다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 부착성 생물을 방오-유효량의 일반식(Ⅰ)의 화합물과 접촉시킴을 특징으로 하여, 수중 표면의 부착성 생물의 부착을 퇴치 또는 구제하는 방법.상기 식에서, X는 할로겐, CN, NO2또는 S(O)nR1이고; Y는 수소, 할로겐 또는 S(O)nR1이며; Z는 할로겐, C1-C4할로알킬 또는 S(O)nR1이며; n은 0,1 또는 2의 정수이며; R1은 C1-C4할로알킬이며; L은 수소 또는 할로겐이며; M 및 Q는 각각 독립적으로 수소, 할로겐, C1-C4알킬, C1-C4할로알킬, C1-C4-알콕시, C1-C4알킬티오, C1-C4알킬설피닐, C1-C4알킬설포닐, CN, NO2, R2CO 또는 NR3R4이거나 M 및 Q가 근접한 위치에 있고 이들이 부착된 탄소원자와 함께 취해질때 MQ는 -OCH2O-, OCF2O- 또는 -CH=CH-CH=CH-의 구조를 나타내며; R은 수소, C1-C4알콕시알킬, C1-C4알킬티오 또는 R6CO이며; R2는 C1-C4알킬, C1-C4할로알킬, C1-C4알콕시 또는 NR3R4이며; R3는 수소 또는 C1-C4알킬이며; R4는 수소 C1-C4알킬 또는 R5CO이며; R5는 수소 또는 C1-C4알킬이며; R6는 C1-C4알킬, C1-C4할로알킬, C1-C4알콕시, C2-C6알케닐옥시, C1-C4할로알콕시, 1 내지 3개의 C1-C4알킬기로 임의로 치환된 페닐, 벤질, 페녹시, 벤질옥시, C1-C4알킬카보닐옥시, C3-C6시클로알킬, 나프틸, 피리딜, 티에닐 또는 푸라닐이다.
- 제1항에 있어서, 부착성 생물이 바나클, 지브라 머슬스, 조류, 규조류, 히드로층, 브리오조아, 아시디안스, 튜브웜 및 아시아 대합조개로 이루어진 그룹 중에서 선택되는 방법.
- 제1항에 있어서, 일반식(Ⅰ)의 화합물이 4,5-디클로로-2-(a,a,a-트리플루오로-파라-트릴)피롤-3-카보니트릴; 4-브로모-5-클로로-2-(파라-클로로페닐)피롤-3-카보니트릴; 4-브로모-2-(파라-클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 3,4-디클로로-2-(3,4-디클로로페닐)피롤-5-카보니트릴; 4-클로로-2-(파라-클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 4,5-디브로모-2-(파라-클로로페닐)-3-(트리플루오로메틸-설포닐)피롤; 4-브로모-2-(3,5-디클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 2-(파라-클로로페닐)-5-(트리플루오로메틸)-4-(트리플루오로메틸티오)피롤-3-카보니트릴; 4-브로모-2-(2,3,4-트리클로로페닐)-5-(트리플루오로메틸)-피롤-3-카보니트릴; 4-브로모-2-(2,3,5-트리클로로페닐)-5-(트리플루오로메틸)-피롤-3-카보니트릴; 4-브로모-2-(파라-클로로페닐)-5-(α,α,β,β-테트라플루오로에틸티오)피롤-3-카보니트릴; 4-브로모-2-(메타-플루오로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 2-(3,5-디클로로페닐)-5-(트리플루오로메틸)-4-(트리플루오로메틸티오)피롤-3-카보니트릴; 및 4-브로모-2-(파라-클로로페닐)-5-[(β-브로모-β,α,α-트리플루오로)-에틸티오]피롤-3-카보니트릴로 이루어진 그룹중에서 선택되는 방법.
- 수중 구조물에 방오-유효량의 일반식(Ⅰ)의 화합물을 도포하거나 침투시킴을 특징으로하여, 해수 및 담수 부착성 생물에 의한 오염으로부터 수중 구조물을 보호하는 방법.상기 식에서, X는 할로겐, CN, NO2또는 S(O)nR1이고; Y는 수소, 할로겐 또는 S(O)nR1이며; Z는 할로겐, C1-C4할로알킬 또는 S(O)nR1이며; n은 0, 1 또는 2의 정수이며; R1은 C1-C4할로알킬이며; L은 수소 또는 할로겐이며; M 및 Q는 각각 독립적으로 수소, 할로겐, C1-C4알킬, C1-C4할로알킬, C1-C4알콕시, C1-C4알킬티오, C1-C4알킬설피닐, C1-C4알킬설포닐, CN, NO2, R2CO 또는 NR3R4이거나 M 및 Q가 근접한 위치에 있고 이들이 부착된 탄소원자와 함께 취해질때 MQ는 -OCH2O-, -OCF2O- 또는 -CH=CH-CH=CH-의 구조를 나타내며; R은 수소, C1-C4알콕시알킬, C1-C4알킬티오 또는 R6CO이며; R2는 C1-C4알킬, C1-C4할로알킬, C1-C4알콕시 또는 NR3R4이며; R3는 수소 또는 C1-C4알킬이며; R4는 수소, C1-C4알킬 또는 R5CO이며; R5는 수소 또는 C1-C4알킬이며; R6는 C1-C4알킬, C1-C4할로알킬, C1-C4알콕시, C2-C6알케닐옥시, C1-C4할로알콕시, 1 내지 3개의 C1-C4알킬기로 임의로 치환된 페닐, 벤질, 페녹시, 벤질옥시, C1-C4 알킬카보닐옥시, C3-C6 시클로알킬, 나프틸, 피리딜, 티에닐 또는 푸라닐이다.
- 제4항에 있어서, 수중 구조물이 어망, 보트, 선박, 적재물, 방파제, 흡입구, 간막이, 냉각탑 파이프 라인 또는 저수탑인 방법.
- 제6항에 있어서, 해수 및 담수 부착성 생물이 바나클, 지브라 머슬스, 조류, 규조류, 히드로층, 브리오조아, 아시디안스, 튜브웜 및 아시아 대합조개로 이루어진 그룹중에서 선택되는 방법.
- 제4항에 있어서, 일반식(Ⅰ)의 화합물이 4,5-디클로로-2-(α,α,α-트리플루오로-파라-토릴)피롤-3-카보니트릴; 4-브로모-5-클로로-2-(파라-클로로페닐)피롤-3-카보니트릴; 4-브로모-2-(파라-클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 3,4-디클로로-2-(3,4-디클로로페닐)피롤-5-카보니트릴; 4-클로로-2-(파라-클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 4,5-디브로모-2-(파라-클로로페닐)-3-(트리플루오로메틸-설포닐)피롤; 4-브로모-2-(3,5-디클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 2-(파라-클로로페닐)-5-(트리플루오로메틸)-4-(트리플루오로메틸티오)피롤-3-카보니트릴; 4-브로모-2-(2,3,4-트리클로로페닐)-5-(트리플루오로메틸)-피롤-3-카보니트릴; 4-브로모-2-(2,3,5-트리클로로페닐)-5-(트리플루오로메틸)-피롤-3-카보니트릴; 4-브로모-2-(파라-클로로페닐)-5-(α,α,β,β-테트라플루오로에틸티오)피롤-3-카보니트릴; 4-브로모-2-(메타-플루오로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 2-(3,5-디클로로페닐)-5-(트리플루오로메틸)-4-(트리플루오로메틸티오)피롤-3-카보니트릴; 및 4-브로모-2-(파라-클로로페닐)-5-[(β-브로모-β,α,α-트리플루오로)-에틸티오]피롤-3-카보니트릴로 이루어진 그룹중에서 선택되는 방법.
- 수중에서 허용되는 불활성 담체 또는 희석제 및 방오-유효량의 일반식(Ⅰ)의 화합물로 이루어짐을 특성으로 하는 해수 및 담수 방오성 조성물.상기 식에서, X는 할로겐, CN, NO2또는 S(O)nR1이고; Y는 수소, 할로겐 또는 S(O)nR1이며; Z는 할로겐, C1-C4할로알킬 또는 S(O)nR1이며; n은 0, 1 또는 2의 정수이며; R1은 C1-C4할로알킬이며; L은 수소 또는 할로겐이며; M 및 Q는 각각 독립적으로 수소, 할로겐, C1-C4알킬, C1-C4할로알킬, C1-C4알콕시, C1-C4알킬티오, C1-C4알킬설피닐, C1-C4알킬설포닐, CN, NO2, R2CO 또는 NR3R4이거나 M 및 Q가 근접한 위치에 있고 이들이 부착된 탄소원자와 함께 취해질 때 MQ는 -OCH2O-, -OCF2O- 또는 -CH=CH-CH=CH-의 구조를 나타내며; R은 수소, C1-C4알콕시알킬, C1-C4알킬티오 또는 R6CO이며; R2는 C1-C4알킬, C1-C4할로알킬, C1-C4알콕시 또는 NR3R4이며; R3는 수소 또는 C1-C4알킬이며; R4는 수소, C1-C4알킬 또는 R5CO이며; R5는 수소 또는 C1-C4알킬이며; R6는 C1-C4알킬, C1-C4할로알킬, C1-C4알콕시, C2-C6알케닐옥시, C1-C4할로알콕시, 1 내지 3개의 C1-C4알킬기로 임의로 치환된 페닐, 벤질, 페녹시, 벤질옥시, C1-C4알킬카보닐옥시, C3-C6시클로알킬, 나프틸, 피리딜, 티에닐 또는 푸라닐이다.
- 제8항에 있어서, L이 수소 또는 할로겐이고, M 및 Q가 각각 독립적으로 수소, 할로겐 또는 C1-C4 할로알킬인 조성물.
- 제8항에 있어서, 일반식(Ⅰ)의 화합물이 4,5-디클로로-2-(α,α,α-트리플루오로-파라-토릴)피롤-3-카보니트릴; 4-브로모-5-클로로-2-(파라-클로로페닐)피롤-3-카보니트릴; 4-브로모-2-(파라-클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 3,4-디클로로-2-(3,4-디클로로페닐)피롤-5-카보니트릴; 4-클로로-2-(파라-클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 4,5-디브로모-2-(파라-클로로페닐)-3-(트리플루오로메틸-설포닐)피롤; 4-브로모-2-(3,5-디클로로페닐)-5-(트리플루오로메틸)피롤-3-카보니트릴; 2-(파라-클로로페닐)-5-(트리플루오로메틸)-4-(트리플루오로메틸티오)피롤-3-카보니트릴; 4-브로모-2-(2,3,4-트리클로로페닐)-5-(트리플루오로메틸)-피롤-3-카보니트릴; 4-브로모-2-(2,3,5-트리클로로페닐)-5-(트리플루오로메틸)-피롤-3-카보니트릴; 4-브로모-2-(파라-클로로페닐)-5-(α,α,β,β-테트라플루오로에틸티오)피롤-3-카보니트릴; 4-브로모-2-(메타-플루오로페닐)-5-(트리플루오로메틸(피롤-3-카보니트릴; 2-(3,5-디클로로페닐)-5-(트리플루오로메틸)-4-(트리플루오로메틸티오)피롤-3-카보니트릴; 및 4-브로모-2-(파라-클로로페닐)-5-[(β-브로모-β,α,α-트리플루오로)-에틸티오]피롤-3-카보니트릴로 이루어진 그룹중에서 선택되는 조성물.※ 참고사항 : 최초출원 내용에 의거하여 공개하는 것임.
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US08/448,240 US5932520A (en) | 1995-05-23 | 1995-05-23 | Use of pyrrole compounds as antifouling agents |
US08/448,240 | 1995-05-23 |
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KR960040155A true KR960040155A (ko) | 1996-12-17 |
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US (1) | US5932520A (ko) |
EP (1) | EP0746979B1 (ko) |
JP (1) | JP4098375B2 (ko) |
KR (1) | KR100443180B1 (ko) |
CN (1) | CN1111354C (ko) |
AR (1) | AR002077A1 (ko) |
AT (1) | ATE271313T1 (ko) |
AU (1) | AU716080B2 (ko) |
BR (1) | BR9602387A (ko) |
CL (1) | CL2011002133A1 (ko) |
DE (1) | DE69632936T2 (ko) |
DK (1) | DK0746979T3 (ko) |
ES (1) | ES2224153T3 (ko) |
IL (1) | IL118350A (ko) |
MY (1) | MY120668A (ko) |
NO (1) | NO316025B1 (ko) |
NZ (1) | NZ286628A (ko) |
PT (1) | PT746979E (ko) |
SG (1) | SG40869A1 (ko) |
SI (1) | SI0746979T1 (ko) |
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EP0831134A1 (en) * | 1996-09-19 | 1998-03-25 | Sigma Coatings B.V. | Light- and bright-coloured antifouling paints |
DE10106455A1 (de) * | 2001-02-13 | 2002-08-14 | Bayer Ag | DELTA·1·-Pyrroline |
JP4666914B2 (ja) * | 2001-11-08 | 2011-04-06 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 4−ブロモ−2−(4−クロロフェニル)−5−(トリフルオロメチル)−1h−ピロール−3−カルボニトリルを含む相乗性防汚組成物 |
DE102005011990A1 (de) * | 2005-03-14 | 2006-09-21 | Basf Ag | Foulingresistente Polyurethane, insbesondere für maritime Anwendungen |
PE20070341A1 (es) * | 2005-07-29 | 2007-04-13 | Wyeth Corp | Derivados de pirrol como moduladores del receptor de progesterona |
PE20070182A1 (es) * | 2005-07-29 | 2007-03-06 | Wyeth Corp | Derivados cianopirrol-fenil amida como moduladores del receptor de progesterona |
TWI399173B (zh) | 2006-02-01 | 2013-06-21 | Janssen Pharmaceutica Nv | 4-溴-2-(4-氯苯基)-5-(三氟甲基)-1h-吡咯-3-腈及金屬化合物之組合物 |
US7893047B2 (en) * | 2006-03-03 | 2011-02-22 | Arch Chemicals, Inc. | Biocide composition comprising pyrithione and pyrrole derivatives |
JP5119238B2 (ja) * | 2006-04-10 | 2013-01-16 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 4−ブロモ−2−(4−クロロフェニル)−5−(トリフルオロメチル)−1h−ピロール−3−カルボニトリルおよび殺生物性化合物の組み合わせ |
DE602007003105D1 (de) * | 2006-08-07 | 2009-12-17 | Janssen Pharmaceutica Nv | Kombinationen aus 4-brom-2-(4-chlorphenyl)-5-(trifluormethyl)-1h-pyrrol-3-carbonitril und oxidierungsmitteln |
EP2348853B1 (en) | 2008-10-08 | 2015-08-19 | Janssen Pharmaceutica N.V. | High solid dispersions comprising biocides |
TW201033308A (en) * | 2008-12-11 | 2010-09-16 | Janssen Pharmaceutica Nv | Antifouling combination comprising 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile |
SG186326A1 (en) * | 2010-07-01 | 2013-01-30 | Janssen Pharmaceutica Nv | Antifouling benzoate combinations |
US20150086719A1 (en) * | 2012-03-07 | 2015-03-26 | Janssen Pharmaceutica, Nv | Use of tralopyril against marine woodborers |
CN104370985B (zh) * | 2014-09-30 | 2020-04-28 | 上海化学试剂研究所有限公司 | 一种类辣椒素类化合物及其制备方法和应用 |
CN104230916B (zh) * | 2014-09-30 | 2020-04-28 | 上海化学试剂研究所有限公司 | 一种异噻唑啉酮类化合物及其制备方法和应用 |
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US4737510A (en) * | 1986-09-30 | 1988-04-12 | The Board Of Trustees Of The University Of Illinois | Bioactive metabolites from the caribbean sponge agelas coniferin |
US5455263A (en) * | 1987-07-29 | 1995-10-03 | American Cyanamid Company | Methods for the control and the protection of warm-blooded animals against infestation and infection by helminths, acarids and arthropod endo- and ectoparasites |
US4929634A (en) * | 1987-10-23 | 1990-05-29 | American Cyanamid Company | Method of and bait compositions for controlling mollusks |
DE3814479A1 (de) * | 1988-04-29 | 1989-11-09 | Bayer Ag | 3-cyano-4-phenyl-pyrrol-derivate, verfahren zu ihrer herstellung und ihre verwendung in schaedlingsbekaempfungsmitteln |
JPH02147669A (ja) * | 1988-11-30 | 1990-06-06 | Nippon Soda Co Ltd | 防汚剤 |
JPH02173165A (ja) * | 1988-12-27 | 1990-07-04 | Nippon Soda Co Ltd | 防汚剤 |
US5328928A (en) * | 1990-05-11 | 1994-07-12 | American Cyanamid Company | N-acylated arylpyrroles useful as insecticidal, agents |
US5157047A (en) * | 1990-10-18 | 1992-10-20 | American Cyanamid Company | Bis- and tris(trifluoromethyl)arylpyrrole insecticidal and acaricidal agents |
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Publication number | Publication date |
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CL2011002133A1 (es) | 2012-02-24 |
CN1111354C (zh) | 2003-06-18 |
ES2224153T3 (es) | 2005-03-01 |
SG40869A1 (en) | 1997-06-14 |
TW416832B (en) | 2001-01-01 |
US5932520A (en) | 1999-08-03 |
AU5237296A (en) | 1996-12-05 |
DE69632936T2 (de) | 2004-12-16 |
SI0746979T1 (en) | 2004-12-31 |
CN1145170A (zh) | 1997-03-19 |
ATE271313T1 (de) | 2004-08-15 |
EP0746979A1 (en) | 1996-12-11 |
IL118350A (en) | 2002-07-25 |
ZA964010B (en) | 1997-11-20 |
JP4098375B2 (ja) | 2008-06-11 |
IL118350A0 (en) | 1996-09-12 |
AR002077A1 (es) | 1998-01-07 |
KR100443180B1 (ko) | 2004-10-08 |
AU716080B2 (en) | 2000-02-17 |
EP0746979B1 (en) | 2004-07-21 |
MY120668A (en) | 2005-11-30 |
NO316025B1 (no) | 2003-12-01 |
JPH092908A (ja) | 1997-01-07 |
NO962091D0 (no) | 1996-05-22 |
DK0746979T3 (da) | 2004-09-06 |
NO962091L (no) | 1996-11-25 |
DE69632936D1 (de) | 2004-08-26 |
BR9602387A (pt) | 1998-04-22 |
NZ286628A (en) | 1998-07-28 |
PT746979E (pt) | 2004-10-29 |
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