Abstract: There are disclosed compounds of the formula ##STR1## wherein R.sub.1 is selected from the group consisting of lower alkyl; R.sub.8 is selected from the group consisting of --O--(CH.sub.2).sub.n --wherein n is 2 to 20, ##STR2## and ##STR3## and R.sub.6 is selected from the group consisting of hydrogen or lower alkoxy, and ##STR4## wherein R.sub.1 is selected from the group consisting of lower alkyl; R.sub.8 is selected from the group consisting of --O--(CH.sub.2).sub.n --wherein n is 2 to 20, ##STR5## and ##STR6## and R.sub.6 is selected from the group consisting of hydrogen or lower alkoxy and racemates thereof.There are also disclosed processes and intermediates utilized to produce the end products.The end products have utility as agents exhibiting both .alpha. and selective .beta. adrenergic blocking action.
Abstract: Unsaturated compounds corresponding to the following formula: ##STR1## in which: R' represents a hydrogen atom or a methyl radical are provided as antioxidant monomers from which antioxidant polymers can be prepared.
Type:
Grant
Filed:
October 16, 1979
Date of Patent:
July 28, 1981
Assignee:
L'Oreal
Inventors:
Bernard Jacquet, Claude Mahieu, Christos Papantoniou
Abstract: N-methyl-N-(benzene sulfonic acid methylamide-N'-sulfenyl)-carbamic acid esters of the formula ##STR1## in which X is halogen, C.sub.1 -C.sub.6 alkyl or hydrogen, andR is a phenyl, naphthyl, benzodioxolanyl or indanyl radical optionally carrying at least one alkyl, alkenyl, alkynyl, alkoxy, alkenoxy, alkynoxy, alkylmercapto, alkenylmercapto, alkynylmercapto, dialkylamino, trihalogenemethyl, halogeno, nitro, nitrile, cycloalkyl, formamidino, dioxanyl or dioxolanyl radical; or an oxime radical of the formula ##STR2## in which R.sup.1 and R.sup.2 each individually is alkyl, alkoxy, alkylthio or alkoxycarbonyl, the alkyl moieties of R.sup.1 and R.sup.2 optionally being linked to one another,which possess insecticidal and acaricidal properties.
Type:
Grant
Filed:
January 27, 1976
Date of Patent:
July 28, 1981
Assignee:
Bayer Aktiengesellschaft
Inventors:
Peter Siegle, Engelbert Kuhle, Ingeborg Hammann, Wolfgang Behrenz
Abstract: The present invention provides novel 19-hydroxy-19-methyl-6a-carba-PGI.sub.1 sulfonylamides which are useful for pharmacological purposes, e.g., anti-asthmatic indications.
Abstract: Liquid petroleum hydrocarbon blends having improved thermal stability at temperatures of 1000.degree. F. and higher are prepared by removing from the blends dissolved molecular oxygen and maintaining low levels of certain trace impurities in the blends. Trace impurity compounds that are maintained at low levels include: sulfur compounds classed as thiols, sulfides, disulfides and polysulfides; organic oxygen compounds classed as hydroperoxides, peroxides, paraffinic carboxylic acids, and phenols; nitrogen compounds classed as amides and alkyl-pyridines; and reactive olefins. Additional improvements in the blends can be obtained by providing them with a dibenzothiophene or a nitrogen compound classed as a paraffinic amine, carbazole or piperidine. The treated blends of this invention have substantially the same physical properties as similar blends that have not been so treated.
Abstract: 2,4-Dinitrophenyl urea is obtained in a technologically simple manner with high yield, if 2,4-dinitro-1-chlorobenzene 1s reacted with cyanamide, advantageously in an excess amount, at a temperature at from about 55.degree. to 75.degree. C. to yield 2,4-dinitrophenyl cyanamide which is subsequently hydrolyzed without intermediate isolation in an aqueous acid medium at a temperature of from about 40.degree. to 75.degree. C. 2,4-Dinitrophenyl urea serves as starting compound for the preparation of 5-amino-benzimidazolones which may be employed, for example, when preparing azo compounds.
Abstract: Tris(aminomethyl)phosphine oxide and its ternary salts, useful as catalysts for the chemical finishing of cotton, are prepared by the hydrolysis of tris(N-carbalkoxylaminomethyl)-phosphine oxides having the formula (RO.sub.2 CNHCH.sub.2).sub.3 PO with an alkali or alkaline earth in the presence of water, followed optionally by acidification.
Type:
Grant
Filed:
March 10, 1980
Date of Patent:
July 14, 1981
Assignee:
The United States of America as represented by the Secretary of Agriculture
Inventors:
Arlen W. Frank, Donald J. Daigle, Russell M. H. Kullman
Abstract: The present invention provides novel 19-keto-PG amides, which are useful for a variety of pharmacological purposes, e.g., antiasthmatic indications.
Abstract: The present invention provides novel 19,20-didehydro-13,14-dihydro-PG.sub.2, sulfonyl amides, methods for their preparation and pharmacological use for the induction of prostaglandin-like effect.
Abstract: Bis(sulfonamides) containing one or more hindered phenol groups are disclosed, as is their use as thermal stabilizers for polymers. Further stabilization results from combinations thereof with a thiodipropionate ester and a divalent metal salt of a carboxylic acid.
Abstract: The present invention provides novel 19,20-didehydro-PG.sub.2 sulfonyl amides, methods for their preparation, and pharmacological use for the induction of prostaglandin-like effect.
Abstract: N-(Substituted-phenyl)-N'-(2-chloro-6-fluoro-benzoyl)- ureas of the formula ##STR1## in which R represents halogenoalkyl with 1-4 carbon atoms,R.sup.1 represents hydrogen, halogen or halogenoalkyl with 1-4 carbon atoms,X represents oxygen or sulphur, andn represents the number 1 or 2which possess insecticidal properties.
Type:
Grant
Filed:
February 1, 1980
Date of Patent:
July 7, 1981
Assignee:
Bayer Aktiengesellschaft
Inventors:
Wilhelm Sirrenberg, Erich Klauke, Albrecht Marhold, Ingeborg Hammann, Wilhelm Stendel, Ingomar Krehan
Abstract: The present invention provides novel 19,20-didehydro-PG.sub.1, sulfonyl amides methods for their preparation and pharmacological use for the induction of prostaglandin-like effect.
Abstract: Acylurea insecticides and methods of preparation thereof are disclosed. The acylureas have compositions of the general formula ##STR1## wherein R.sub.1 is halogen, alkyl with from 1 to 6 carbon atoms or alkoxy with from 1 to 6 carbon atoms; R.sub.2 is hydrogen or halogen; R.sub.3 is hydrogen or alkyl with from 1 to 6 carbon atoms; R.sub.4 is hydrogen, alkyl with from 1 to 6 carbon atoms, aryl with from 6 to 12 carbon atoms, halogen substituted aryl with from 6 to 12 carbon atoms or alkaryl with from 7 to 12 carbon atoms; R.sub.5 is halogen; R.sub.6 is hydrogen or halogen; X is halogen or alkyl with from 1 to 6 carbon atoms; and n is 0, 1 or 2.
Abstract: The present invention provides novel 19-keto-PG sulfonylamides, which are useful for a variety of pharmacological purposes, e.g., antiasthmatic indications.
Abstract: N-(4-Substituted-phenyl)-N'-(2-substituted-benzoyl)-thioureas of the formula ##STR1## in which R.sup.1 represents halogen,R.sup.2 represents hydrogen or halogen,R.sup.3 represents hydrogen, halogen or halogenoalkyl,R.sup.4 represents halogen, halogenoalkyl, halogenoalkoxy, halogenoalkylthio or halogenoalkylsulphonyl, with the proviso that R.sup.3 represents halogenoalkyl if R.sup.4 represents halogen, andR.sup.5 represents hydrogen or halogen,which possess arthropodicidal, fungicidal and bactericidal properties.
Type:
Grant
Filed:
August 16, 1979
Date of Patent:
June 30, 1981
Assignee:
Bayer Aktiengesellschaft
Inventors:
Wilhelm Sirrenberg, Erich Klauke, Ingeborg Hammann, Ingomar Krehan, Peter Kraus, Wilhelm Stendel
Abstract: The present invention provides novel 19,20-didehydro-13,14-dihydro-PG.sub.1, sulfonyl amides, methods for their preparation and pharmacological use for the induction of prostaglandin-like effect.
Abstract: N-alkynylanilides, a process for their preparation, fungicidal compositions containing the N-alkynylanilides as the active ingredient and methods for the use of such compounds or compositions for combatting plant fungi are disclosed.
Abstract: 1-Indanyloxy- or tetrahydronaphthyloxy-3-amino-2-butanol derivatives, especially erythro-1-(7-methylindan-4-yloxy)-3-isopropylaminobutan-2-ol, processes for their manufacture and pharmaceutical compositions containing them. The compounds possess peripherally-selective .beta.-adrenergic blocking activity.