RELATION BETWEEN STRUCTURE AND HERBICIDAL ACTIVITY OF SUBSTITUTED BENZONITRILES
作者:
H. KOOPMAN,
J. DAAMS,
期刊:
Weed Research
(WILEY Available online 1965)
卷期:
Volume 5,
issue 4
页码: 319-326
ISSN:0043-1737
年代: 1965
DOI:10.1111/j.1365-3180.1965.tb00359.x
出版商: Blackwell Publishing Ltd
数据来源: WILEY
摘要:
Summary.The herbicidal activity of substituted benzonitriles was determined by a number of tests. This activity was compared with the structure of the molecules. It was found experimentally that benzonitriles, substituted at the 2 and 6 positions by halogen or methyl, had the highest activity. Some 2,6‐dichloro‐1‐substituted benzene derivatives showed a herbicidal activity, comparable with that of 2,6‐dichlorobenzonilrile. These compounds possessed a group which could be converted into a nitrilc group.La relation entre la structure ft l'activité herbicide des benzonitril‐es
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