Abstract:
2-AMINO-AZACYCLOTRIADECENES IN WHICH THE NITROGEN ATOM OF THE AMINO GROUP IS UNSUBSTITUTED OR BEARS CERTAIN SUBSTITUENTS AS WELL AS THEIR ADDITION SALTS WITH ACIDS ARE DESCRIBED AS ANTIFUNGAL AGENTS THE EFFECTIVENESS OF WHICH IS CONSIDERABLY SUPERIOR TO THAT OF THE KNOWN 2-AMINOAZACYCLOPHEPTENES. A TYPICAL COMPOUND IS 2-N-BUTYLAMINOAZACYCLOTRIDEC-1-ENE.
Abstract:
Derivatives of malonic acid substituted with groups containing a hindered phenol are disclosed. A preferred compound is di-noctadecyl-2,2-bis-(3'',5''-di-t-butyl-4''-hydroxybenzyl) malonate. The compounds are stabilizers suitable for stabilizing numerous substrates of organic material subject to oxidative deterioration, in particular polypropylene. Synergistic combinations of these compounds and dialkyl thiodipropionates are disclosed.
Abstract:
Photochromic 1,3,6,8-tetra(lower)alkyl-15,16-dimethyl-15,16dihydropyrenes, 15,16-methylene-15,16-dihydropyrenes, 15,16methylene-15,16-dihydropyrenes and 1,3,6,8-tetra(lower)alkyl15,16-methylene-15,16-dihydropyrenes substituted in one or both of the 2- and 7-positions benzoyl, alkanoyl, alkanoyloxy, cyano, nitro, alkyl, Alpha -hydroxyalkyl, Alpha -acyloxyalkyl, Alpha -isonitrosoalkyl, or acylamido groups are prepared via substitution of the parent hydrocarbon. A typical embodiment is 2-acetamido-7-nitro-1,3,6,8,15,16-hexamethyl-15,16dihydropyrene.
Abstract:
Pyridyl-(2)-phosphates and phosphorothioates are disclosed which have in 5-position at the pyridine nucleus a thiazolinyl-(2) grouping and which are insecticidal and acaricidal agents useful in the control of insects and acarinae, and more particularly of cattle ticks. Compositions containing these novel compounds, methods for controlling insects and acarinae therewith, and novel 2-hydroxy- and 2-mercapto-5-thiazolinyl-(2'')-pyridines useful as intermediates in their production are also described.
Abstract:
N-benzylidene alkylamines in which the alkyl group has from eight to 18 carbon atoms, and in which the phenyl moiety is optionally substituted, are fungicidal agents. Compositions containing these compounds are fungicides and methods for combatting fungi use these compounds.
Abstract:
The production of 5-(2-methylene-alkanoyl)-benzofuran-, 5-(2methylene-alkanoyl)-indole- and 5-(2-methylene-alkanoyl)benzo(b)thiophene-2-carboxylic acids by reaction of the corresponding 5-(2-dimethylaminomethyl-alkanoyl)- derivatives with sodium acetate in the glacial acetic acid and their pharmaceutically acceptable salts with bases, a method of producing a diuretic and saluretic effect in mammals comprising administering said compounds to said mammals and pharmaceutical compositions containing said compounds are described. A typical embodiment is 5-(2-methylene-butyryl)-6-methyl-benzofuran-2carboxylic acid.
Abstract:
Pharmaceutical compositions suitable for oral administration are prepared from non-ionisable polycyclic bases, an ion-exchange resin containing carboxylic acid groups and a pharmaceutically acceptable carrier liquid. These compositions are used for producing an anti-depressant effect in mammals. A typical embodiment is a composition containing imipramine and Zeo-Karb 226.
Abstract:
A METHOD FOR THE PREPARATION OF ALKOXY-BIS(ALKYLAMINO)-S-TRIAZINES BY REACTING HALOGENO-BIS(ALKYLAMINO)S-TRIAZINES WITH ALIPHATIC ALCOHOLS AT ELEVATED PRESSURES IN THE PRESENCE OF A SLIGHT EXCESS OF ALKALI.
Abstract:
AGENTS FOR INHIBITING THE GROWTH OF FUNGI, WHICH CONTAIN AS ACTIVE COMPONENT 5-AMINO-1,2-DITHIOL-3-ONES SUBSTITUTED AT THE AMINO GROUP AND ALSO N 4-POSITION, AND METHOD OF CONTROLLING PHYTOPATHOGENIC AND OTHER NOXIOUS FUNGI WITH SUCH AGENTS, WHICH ARE OF SURPRISINGLY LOW PHYTOXICITY.