Fungicidal azolylethane derivatives
AssigneeBASF SE
InventorsRainer Seele, Norbert Goetz, Wolfgang Brox, Reiner Kober, Eberhard Ammermann, Gisela Lorenz
Life of this patent
Estimating the term…
Abstract
Azolylethane derivatives of the formula I ##STR1## where A and R.sup.1 are each alkyl, phenyl, biphenyl, naphthyl, benzyl, cycloalkyl, alkoxy, alkylthio, phenoxy, benzyloxy, phenylthio, methoxycarbonylethyl or hetaryl, these radicals being substituted or unsubstituted, D is halogen, alkoxy, alkylthio, phenylthio or phenoxy, these radicals being substituted or unsubstituted, X is CH or N, plant-tolerated acid addition salts and metal complex compounds thereof, and fungicides containing these compounds.
Claims6
A compound of the formula I ##STR197## where A and R.sup.1 are identical or different and are each C.sub.1 -C.sub.8 -alkyl, phenyl, biphenyl, naphthyl, benzyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.8 -alkylthio, phenoxy, benzyloxy, phenylthio, methoxycarbonylethyl, furyl or thienyl, and these radicals may be monosubstituted to trisubstituted by halogen, nitro, phenoxy, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -haloalkyl,
- with the proviso that at least one of the substituents A and R.sup.1 is furyl or thienyl, each of which is unsubstituted or mono- to trisubstituted by halogen, nitro, phenoxy, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -haloalkyl,
- D is halogen, and
- X is N,
- or its plant-tolerated acid addition salts or metal complex compounds.
A fungicidal composition comprising an inert carrier and a fungicidally effective amount of an azolylethane derivative of the formula I ##STR198## where A and R.sup.1 are identical or different and are each C.sub.1 -C.sub.8 -alkyl, phenyl, biphenyl, naphthyl, benzyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.8 -alkylthio, phenoxy, benzyloxy, phenylthio, methoxycarbonylethyl, furyl or thienyl, and these radicals may be monosubstituted to trisubstituted by halogen, nitro, phenoxy, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -haloalkyl,
- with the proviso that at least one of the substituents A and R.sup.1 is furyl or thienyl, each of which is unsubstituted or mono- to trisubstituted by halogen, nitro, phenoxy, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -haloalkyl,
- D is halogen, and
- X is N,
- or a plant-tolerated acid addition salt or metal complex thereof.
A process for combating fungi, wherein a fungicidally effective amount of an azolylethane derivative of the formula I ##STR199## where A and R.sup.1 are identical or different and are each C.sub.1 -C.sub.8 -alkyl, phenyl, biphenyl, naphthyl, benzyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.8 -alkylthio, phenoxy, benzyloxy, phenylthio, methoxycarbonylethyl, furyl or thienyl, and these radicals may be monosubstituted to trisubstituted by halogen, nitro, phenoxy, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -haloalkyl,
- with the proviso that at least one of the substituents A and R.sup.1 is furyl or thienyl, each of which is unsubstituted or mono- to trisubstituted by halogen, nitro, phenoxy, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -haloalkyl,
- D is halogen, and
- X is N,
- or its plant-tolerated acid addition salt or metal complex thereof, is allowed to act on fungi, or plants, or plant habitat, plant materials, timber or seed threatened by fungus attack.
Dependencies are inferred from the claim text.