## Abstract The synthesis of some heterocyclic‐aromatic sulphones with potential acaricidal properties is described. The benzene nucleus in these sulphones is substituted either with a __para__‐chlorine atom or with three chlorine atoms in positions 2, 4 and 5. The heterocyclic nuclei used are pyri
Synthesis and physiological properties of some heterocyclic-aromatic sulphides and sulphones: IV Biological investigations
✍ Scribed by P. A. van Zwieten; J. Meltzer; H. O. Huisman
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 277 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
The acaricidal properties of some new halogen‐substituted heterocyclic‐aromatic sulphides and sulphones are described. As a rule, the adulticidal activity is negligible, though some compounds show interesting ovicidal properties. The sulphides possess a higher ovicidal activity than the sulphones. The pyridyl sulphides are the most active, the thiazolyl sulphides somewhat less, whereas the pyrimidyl and thienyl sulphides are almost inactive. The pyridine‐N‐oxides are also inactive. The polarity of the compounds synthesized seems to exert a considerable influence on the ovicidal properties.
📜 SIMILAR VOLUMES
## Abstract The preparation of some aryl‐pyridyl sulphides with potential acaricidal properties is described. In the compounds synthesized the benzene nucleus is substituted with a __para__‐chlorine atom or with three chlorine atoms in positions 2, 4 and 5. Position 5 in the pyridine nucleus is eit
## Abstract The synthesis of some heterocyclic‐aromatic sulphides with potential acaricidal properties is described. The benzene nucleus in these sulphides is substituted either with a __para__‐chlorine atom or with three chlorine atoms in positions 2,4 and 5. The heterocyclic nuclei are pyrimidine