Sandoz Gmbh

Velsicol Chemical Corporation

Basf Se Corporation

Merial Limited

Cropsolution, Inc.

Boehringer Ingelheim Animal Health USA Inc.

Takeo Hokama

Leonard J Stach

Louis G Nickell

Ian S Cloudsdale

Richard J Anderson

Henricus Maria Martinus Bastiaans

Matthias Pohlman

Frank Scardiglia

Christopher Palmer

Michael Rack

Deborah L Culbertson

Hassan Oloumi-Sadeghi

Michael Hofmann

Ralph Paulini

Anna Malveda Umali

Rhoel Suiza Cosare

Cecille Ebuenga Doyog

Sebastian Soergel

Charles Q Meng

Mark Soll

James T Traxler

Jürgen Langewald

Hermann Schneider

Sarah Thompson

Shy-Fuy Lee

Sebastian Sörgel

Richard Anderson

Vivian Du

Christian Miculka

Werner Langer

Patricia Arakaki

Rafael Oey

Sarah Rachel Devereux

Henricus Maria Bastiaans

Henricus Maria Bastiaanns

Sebastian Sorgel

Charles Meng

Henricus Maria Martinus Bastiaanns

The present invention provides uses of aryl alkyl malononitrile compounds of formula (I), or veterinarily acceptable salts thereof, for controlling and preventing parasite infestations in animals. The invention also provides methods for controlling and preventing parasite infestation in animals comprising administering an effective amount of at least one aryl alkyl malononitrile compound of formulae (I), or a veterinarily acceptable salt thereof, to the animal.

Use of malononitrile compounds for protecting animals from parasites

The invention relates to the use of a compound of formula (I) or a salt thereof for combating animal pests,where the symbols and indices are defined in the specification.

Malononitrile compounds for controlling animal pests

Compounds of formula I wherein X is O or S(&#x2550;O); n is 0, 1 or 2; Ris optionally substituted alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, phenyl, hetaryl, phenylalkyl, hetaryl alkyl, optionally fused to phenyl, hetaryl or heterocyclyl; A is &#x2014;NR, &#x2014;C(=G)GR, &#x2014;C(=G)NR, &#x2014;C(&#x2550;NOR)R, C(=G)[N&#x2550;SR], &#x2014;C(=G)NRb&#x2014;NR, C-C-alkandiyl, C-C-alkenediyl, C-C-alkyl-G-C-C-alkyl, wherein Ris as defined in the description, or optionally substituted phenyl, hetaryl, heterocyclyl, optionally fused to phenyl or heterocyclyl; B is an optionally substituted saturated or partially unsaturated hydrocarbon chain with 1 to 3 carbon chain atoms; D is an optionally substituted saturated or partially unsaturated hydrocarbon chain with 1 to 5 carbon chain atoms or C-C-cycloalkyl; G is oxygen or sulfur; or the enantiomers or diastereomers or salts or N-oxides thereof, processes for preparing the compounds I, pesticidal compositions and synergistic mixtures comprising compounds I, methods for the control of insects, acarids or nematodes by contacting the pests or their food supply, habitat or breeding grounds with a pesticidally effective amount of compounds formula I, and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective amount of compounds of formula I. 

Malononitrile compounds

Compounds of formula (I) wherein the symbols have the meaning given in the specification, as well as processes for preparing the compounds (I), pesticidal compositions and synergistic mixtures comprising compounds (I), methods for the control of insects, acarids or nematodes by contacting the pests or their food supply, habitat or breeding grounds with a pesticidally effective amount of compounds formula (I), and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective amount of compounds of formula (I).

Compounds of formula I are described: along with compositions thereof, methods of use thereof (particularly as fungicides), and methods of making the same.

3-Aryl-3-hydroxy-2-methylenepropionic acid esters as fungicides

A process for preparation of substituted phthalides, heterocyclic phthalides and derivatives thereof by reacting an aromatic carboxylic acid mono- or di-anion with a reactive derivative of a pyrimidine carboxylic acid.

Process for preparing substituted pyrimidines

Substituted phthalides and heterocyclic phthalides and derivatives thereof which are useful as herbicides are described.

Substituted phthalides and heterocyclic phthalides

The subject matter of this invention involves 2-[4-(2-pyridinyloxy)phenoxy]propionyl-2-oxazolidinones which are substituted in the pyridinyl ring by trifluoromethyl and/or chloro. The compounds are useful for increasing the recoverable sugar in sugarcane.

2-[4-(2-pyridinyloxy)phenoxy]propionyl-2-oxazolidinones

The subject matter of this invention is the use of propanoic esters of the following structural formula: ##STR1## wherein R is an alkyl group having 10 to 16 atoms to increase the recoverable sugar in sugarcane.

Method of increasing the yield of sugar from sugarcane

The subject matter of this invention is the use of 2,4-dichlorophenoxyethyl 2-[4-(3,5-dichloropyridin-2-yloxy)phenoxy]propanoate as a sugarcane ripener.

The subject matter of this invention is the new compound, pent-2-en-4-on-2-yl 2-[4-(5-trifluoromethyl-2-pyridinyloxy)phenoxy]propanoate. This compound is useful for increasing the recoverable sugar in sugarcane.

Pent-2-en-4-on-2-yl

The subject matter of this invention are the following sulfonamides: ##STR1## wherein X is chlorine or trifluoromethyl

Certain 1-(N-methylsulfonamido)-prop-2-yl

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Chicago, IL, United States of America

Takeo Hokama