イミダクロプリドのピリジン環5位にアルコキシ基を持つ誘導体の殺虫活性

• Kagabu Shinzo

  Department of Chemistry, Faculty of Education, Gifu University

• Fujii Yuya

  Department of Chemistry, Faculty of Education, Gifu University

• Nishimura Keiichiro

  Research Institute for Advanced Science and Technology, Osaka Prefecture University

書誌事項

タイトル別名

• Insecticidal activity of imidacloprid derivatives with an alkoxy group at the C5 position of the pyridine ring

抄録

Six derivatives of imidacloprid with an alkoxy group introduced at the fifth position on the pyridine ring were prepared. Minimal lethal doses in mol (MLDs) were determined in American cockroaches both with and without synergists, piperonyl butoxide and propargyl propyl benzenephosphonate. The log(1/MLD) value without synergists was 7.43 for the methoxy substituted derivative. Values for the higher alkyloxy homologues particularly the n-propoxy derivative were lower. Synergists combined enhanced the potency by about one log unit for each compound. The introduction of any alkoxy group does not improve the activity of imidacloprid. © Pesticide Science Society of Japan

収録刊行物

• 日本農薬学会誌（Ｊｏｕｒｎａｌ　ｏｆ　Ｐｅｓｔｉｃｉｄｅ　Ｓｃｉｅｎｃｅ）

  日本農薬学会誌（Ｊｏｕｒｎａｌ　ｏｆ　Ｐｅｓｔｉｃｉｄｅ　Ｓｃｉｅｎｃｅ） 31 (2), 150-155, 2006

  日本農薬学会

キーワード

• neonicotinoid insecticide
• imidacloprid
• American cockroach
• insecticidal activity
• alkoxy-substituted pyridine

詳細情報

• CRID: 1390001205211444736
• NII論文ID: 110004751831
• NII論文ID: 130004445029
• NII書誌ID: AA11818622
• DOI: 10.1584/jpestics.31.150
• ISSN: 13490923
• ISSN: 03851559
• ISSN: 1348589X
• NDL書誌ID: 7922908
• Web Site: https://agriknowledge.affrc.go.jp/RN/2030731650
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I7922908
• Web Site: http://www.jstage.jst.go.jp/article/jpestics/31/2/31_2_150/_pdf
• Web Site: http://dl.ndl.go.jp/info:ndljp/pid/10877770
• Web Site: https://search.jamas.or.jp/link/ui/2006215768
• 本文言語コード: en
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