133980-45-7Relevant academic research and scientific papers
N-(Pyrid-3-yl)thioureas and Derivatives as Acaricides. I. Synthesis and Biological Properties
Pascual, Alfons,Rindlisbacher, Alfred
, p. 253 - 264 (2007/10/03)
In the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N-(pyrid-3-yl)thioureas, isothioureas and -carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.
Aminopyridines
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, (2008/06/13)
Novel 3-amino-2,4-dialkylpyridine derivatives STR1 in which R1 and R2 are each independently C1 -C6 alkyl, R3 is C1 -C12 alkyl, C3 -C6 cycloalkyl, C1 -C4 alkyl substituted by C3 -C6 cycloalkyl, or C3 -C6 cycloalkyl substituted by C1 -C4 alkyl, R4 is hydrogen, halogen, C1 -C6 alkyl, phenoxy, or phenoxy that is mono- or di-substituted by halogen, C1 -C4 alkyl, C1 -C4 alkoxy, C1 -C4 alkylthio, C1 -C4 alkylamino, di-C1 -C4 alkylamino, C1 -C4 alkylcarbonylamino, C1 -C4 alkylcarbonyl, benzoyl, nitro, cyano, C1 -C4 alkoxycarbonyl, C1 -C4 haloalkyl or by C1 -C4 haloalkoxy, and Z is a bridge member --NH--CS--NH--, --N=C(SR5)--NH-- or --N=C=N-- wherein R5 is C1 -C6 alkyl or C3 -C5 alkenyl, can be used as pesticides. Preferably, insects and arachnids can be controlled.
