Synergistic triazole compounds

US4988818A · kind A · utility

Assignee

• BASF SE

Inventors

• Manfred Lauer · Ludwigshafen, DE
• Matthias Zipplies · Hirschberg, DE
• Hubert Sauter · Mannheim, DE
• Barbara A. Moore · Pittsboro, US
• Dale R. Carlson · Hillsborough, US
• Paul S. Zorner · Carlsbad, US
• Karl-Otto Westphalen · Speyer, DE
• Bruno Wuerzer · Otterstadt, DE

Key dates

• Filing date: Oct 6, 1989
• Grant date: Jan 29, 1991
• Expiry date: Oct 6, 2009

Classification

• Technology area (CPC C): Chemistry; Metallurgy
• CPC primary: C07D249/08
• WIPO field: Organic fine chemistry
• WIPO sector: Chemistry

Abstract

Triazole compounds I ##STR1## where A is C.sub.7 -C.sub.20 -alkyl or unsubstituted or substituted phenyl, naphthyl or pyridyl, and R is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -alkenyl or C.sub.3 -C.sub.6 -alkynyl or is --COR.sup.x or --SO.sub.2 R.sup.x, where R.sup.x is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.8 -alkyl or phenyl, and their environmentally compatible salts, and herbicides containing one or more triazole compounds I, IA or IB ##STR2## where R.sup.1 is hydrogen, cyclopropyl or unsubstituted or substituted C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl or C.sub.2 -C.sub.6 -alkynyl or is C.sub.1 -C.sub.4 -alkoxy, C.sub.2 -C.sub.4 -alkenyloxy or C.sub.2 -C.sub.4 -alkynyloxy, and R.sup.2 and R.sup.3 are each hydrogen, adamantyl or C.sub.1 -C.sub.3 -alkyl or, together with the carbon atom to which they are bonded, form unsubstituted or substituted C.sub.3 -C.sub.7 -cycloalkyl, C.sub.6 -C.sub.10 -bicycloalkyl, C.sub.6 -C.sub.10 -bicycloalkenyl, or their environmentally compatible salts and a benzothiadiazone.