Combating arthropods with 2- and 4-substituted-chromanes
Abstract
Abstract Chromane derivatives of the formula <IMAGE> in which R1 to R4, which need not be identical, each represents hydrogen, an optionally substituted alkyl, alkenyl, cycloalkyl, aryl, aralkyl or alkoxycarbonyl radical, carboxyl or aminoalkyl, R2 can alternatively represent amino or optionally substituted dialkylamino, or R1 and R2 conjointly with the adjoining carbon atoms can form an optionally substituted carbocyclic or heterocyclic ring, R5 to R8, which need not be identical, each represents hydrogen, halogen, hydroxyl, nitro, cyano, carboxyl, an optionally substituted alkyl, alkenyl, cycloalkyl, aryl, aralkyl, alkoxy, aralkoxy, aryloxy, alkoxycarbonyl, alkylamino or dialkylamino radical, amino or acylamino, and two of the radicals, which are in the o-position to one another, can represent tetramethylene or the radical -CH=CH-CH=CH-, and X represents OH or the -NR9R10 radical, wherein R9 and R10, which may be identical or different, each represents hydrogen or optionally substituted alkyl, alkenyl, cycloalkyl, aryl or aralkyl, or R9 and R10 conjointly with the adjoining nitrogen atom form a ring which optionally contains one or more further hetero-atoms, or optionally, when X is -NR9R10, a salt thereof, in which X is a hydroxy or amino radical, and R1 to R8 can be hydrogen or various organic radicals, or salts thereof possess arthropodicidal properties. Those compounds wherein R1 and R2 conjointly with the adjoining carbon atoms forms a carbocyclic or heterocyclic ring are new.
Inventors
- 👤 Hans-Joachim Kabbe
- 👤 Arno Widdig
- 👤 Wilhelm Stendel
- 👤 Peter Roessler
Bibliographic Details
Claims Analysis
Total Claims: 5References Cited (Backward Citations)
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