Structure-activity Relationship of Acaricidal tyans-2-(4-tert-Butylphenyl) cyclopropanecarboxylates

Acaricidal activities of cyano-(6-phenoxy-2-pyridyl)methyl traps-3-aryl-2, 2-dimethylcy-clopropanecarboxylates were analyzed quantitatively. An analysis of para-substituents of phenyl ring in the acid moiety by Hansch-Fujita method revealed that substituents having an appropriate hydrophobicity with...

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Bibliographic Details
Published inJournal of Pesticide Science Vol. 11; no. 2; p. 169
Main Authors OZAWA, Kiyomi, ISHII, Shigeru, HIRATA, Kiminori, HIROSE, Masayoshi
Format Journal Article
LanguageEnglish
Published Tokyo Japan Science and Technology Agency 01.04.1986
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Summary:Acaricidal activities of cyano-(6-phenoxy-2-pyridyl)methyl traps-3-aryl-2, 2-dimethylcy-clopropanecarboxylates were analyzed quantitatively. An analysis of para-substituents of phenyl ring in the acid moiety by Hansch-Fujita method revealed that substituents having an appropriate hydrophobicity with branches at α-position, such as tert-butyl group, were preferable to the acaricidal activity. In addition to the acaricidal activity, some compounds suppressed phytophagous insects.
ISSN:1348-589X
1349-0923