Abstract: Novel 2-(phenoxy-.alpha.-alkyl)-imidazolines of the formula ##STR1## wherein R.sub.1 and R.sub.2, each independently of the other, are methyl or chlorine, or together they are --(CH.sub.2).sub.3 or --(CH.sub.2).sub.4 group and R.sub.3 is ethyl, n-propyl or isopropyl, processes for obtaining these compounds and compositions containing them for the control of plant-damaging mites and mites which are parasites of animals.

Abstract: Compounds of the formula ##STR1## wherein R.sub.1 is methyl or ethyl, R.sub.2 is C.sub.1 -C.sub.12 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl or cyclopropylmethyl, R.sub.3 is C.sub.1 -C.sub.4 -alkyl or phenyl optionally mono-, or di- or trisubstituted by halogen and/or methyl and either (i) X.sub.1 is methyl, chlorine, bromine or hydrogen and X.sub.2 is methyl or (ii) X.sub.1 is methyl, chlorine or bromine and X.sub.2 is hydrogen exhibit valuable pesticidal, in particular acaricidal and insecticidal, properties.

Abstract: Compounds of the formula I ##STR1## wherein R.sub.1 and R.sub.2 are each chlorine or methyl, R.sub.3 is hydrogen or C.sub.1 -C.sub.4 -alkyl and R.sub.4 is C.sub.1 -C.sub.6 -alkyl optionally substituted by cyano or phenyl optionally substituted by halogen and/or methyl are novel and are pesticidally in particular acaricidally active.

Abstract: Sulphur-free cyclopeptides with somatostatin-analogous aminoacid partial sequences, of the formula ##STR1## in which R is Asn, Ala or de-R, trp is D-Trp or L-Trp, which can be substituted in the benzene ring by halogen atoms or nitro groups, W is a free or etherified hydroxyl group or halogen atom present as a substituent on the benzene ring of the L-phenylalanine radical, or is hydrogen, X is the radical of an .omega.-amino-lower alkane-(mono or di)-carboxylic acid or de-X and Y is the radical of an .omega.-amino-lower alkane-(mono or di)-carboxylic acid or de-Y, and also acid addition salts and complexes thereof have biological properties similar to those of somatostatin and can be used, especially in the form of pharmaceutical preparations, for the treatment of excessive secretion of somatotropin, insulin and/or glucagon. The compounds according to the invention are obtained by cyclising a corresponding linear peptide compound in which the .epsilon.

Abstract: Cyclopropanecarboxylic acid-phenoxy-.alpha.-vinyl-benzyl esters of the formula ##STR1## in which Y is chlorine or bromine, and R.sub.1 is --CH.dbd.CH.sub.2 or ##STR2## processes for producing them, and their use in combating pests.

Abstract: The substituted 5H-dibenz[b,f]azepine of the formula ##STR1## a process for its manufacture, pharmaceutical compositions which contain the novel compound, and a method of treating epilepsy which comprises the use thereof.

Abstract: Compounds of the formula I ##STR1## wherein R.sub.1 is fluorine or chlorine and R.sub.2 is hydrogen, fluorine or chlorine having valuable insecticidal properties.

Abstract: 6.beta.-(R.sub.a)(R.sub.b)N-methylaryl-acetylamino-6.alpha.-methoxy-2,2-dim ethylpenam-3-carboxylic acid compounds and 7.beta.-(R.sub.a)(R.sub.b)N-methylaryl-acetylamino-7.alpha.-methoxy-3-ceph em-4-carboxylic acid compounds, wherein R.sub.a and R.sub.b independently of each other represent hydrogen or optionally substituted lower alkyl, or wherein R.sub.a and R.sub.b conjointly denote optionally substituted lower alkylene, wherein the aminomethyl-substituted aryl radical represents a corresponding thienyl, furyl or phenyl radical, and wherein the 3-position in 3-cephem compounds is unsubstituted or substituted by a modified hydroxyl group or an optionally substituted methyl group, exhibit antibiotic action against Gram-negative or Gram-positive micro-organisms.

Abstract: Compounds of the formula I ##STR1## wherein R.sub.1 and R.sub.2 are each chlorine or methyl, R.sub.3 is hydrogen or C.sub.1 -C.sub.4 -alkyl and R.sub.4 is cyano or a group of the formula A or B. ##STR2## and their acid addition salts possess useful pesticidal in particular acaricidal properties.

Abstract: Compounds of the formula I ##STR1## wherein R.sub.1 and R.sub.2 are each methyl or chlorine, R.sub.3 is hydrogen or C.sub.1 -C.sub.4 -alkyl, R.sub.4 is methyl or ethyl, R.sub.5 is methoxy, ethoxy, C.sub.1 -C.sub.4 -alkylthio or phenyl and X is oxygen or sulphur have valuable pesticidal in particular acaricidal properties.

Abstract: Dihalovinylcyclopropanethiolic acid esters of the formula ##STR1## wherein X.sub.1 represents fluorine, chlorine or bromine, R.sub.1 represents hydrogen, methyl, ethynyl or cyano, and Y represents hydrogen, fluorine, chlorine or bromine, processes for their manufacture, and a method of controlling pests which comprises the use of these compounds.

Abstract: Compound of the formula I ##STR1## wherein R.sub.1, R.sub.1 ', R.sub.2 and R.sub.2 ' are each chlorine or methyl and R.sub.3 and R.sub.3 ' are each hydrogen or C.sub.1 --C.sub.4 -alkyl possess valuable pesticidal in particular acaricidal properties.

Abstract: Cyclopropanecarboxylic acid esters of the formula ##STR1## in which X.sub.1 is fluorine, chlorine or bromine, R.sub.1 and R.sub.2 are each hydrogen, fluorine, chlorine, bromine or methyl, R.sub.3 and R.sub.4 are each hydrogen, fluorine, chlorine, bromine, methyl, methoxy, nitro or dimethylamine, or together are methylenedioxy, and R.sub.5 is hydrogen or methyl, processes for producing them, and their use in controlling insect pests.

Abstract: Phenylformamidines of the formula ##STR1## wherein R.sub.1, R.sub.2 and R.sub.3 each represent hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or halogen, R.sub.4 represents methyl or ethyl, and R.sub.5 represents C.sub.1 -C.sub.8 -alkyl or C.sub.3 -C.sub.6 -cycloalkyl, processes for producing them, and their use for combating pests.

Abstract: Novel benzothiopyran derivatives of the general formula ##STR1## in which R is free, esterified or amidated carboxyl or free or etherified hydroxymethyl, Ph is 1,2-phenylene which contains the group R--CO--NR.sub.3 -- and can be substituted, X is a group of the formula --CO--CR.sub.1 .dbd.CR.sub.2 --, in which R.sub.1 and R.sub.2 independently of one another are hydrogen, acyl or a substituted or unsubstituted hydrocarbon radical or a hetero-analogue thereof or together are 3-membered to 5-membered lower alkylene, and R.sub.2 can also be free or etherified hydroxyl or hydroxyl esterified by an organic carboxylic acid, and R.sub.3 is hydrogen or lower alkyl, possess antiallergic properties and can be used as medicaments.

Abstract: A process known per se for the manufacture of oxygenated N-aryl-diazacyclic compounds of the formula ##STR1## wherein each of R.sub.1 and R.sub.2 represents a substituted or unsubstituted aryl group and alk represents a lower alkylene group which separates both nitrogen atoms from each other by 2 or 3 carbon atoms, or salts thereof.The novel compounds can be used as antihypertensives, antitachycardiac agents and .alpha.-receptor blockers.

Abstract: The present invention relates to novel benzopyrane derivatives, especially 3-oxaloamino-4-oxo-4H-1-benzopyrane derivatives of the formula I ##STR1## in which Ph is substituted or unsubstituted 1,2-phenylene, R is free, esterified or amidated carboxyl and R.sub.1 is hydrogen or a substituted or substituted hydrocarbon radical, in the free form or in the form of a salt, exhibit antiallergic activities and are accordingly useful as active ingredients of antiallergic pharmaceutical preparations.

Abstract: 3,4-Dihydro-2H-1,2-benzothiazine 1,1-dioxides of the formula ##STR1## wherein Ph represents a substituted or unsubstituted 1,2-phenylene radical, R represents a substituted or unsubstituted benzopyrone radical, and R.sub.1 represents hydrogen or a substituted or unsubstituted hydrocarbon radical of aliphatic character, and their salts, possess antiinflammatory properties and are useful as medicaments.

Abstract: New heterocyclylcarboxylic acid derivatives which are acylated in the nucleus, especially benz-acyl-benzimidazole-2-carboxylic acid derivatives of the formula ##STR1## in which R is a free, esterified or amidated carboxyl group or a free, etherified or esterified hydroxymethyl group, R.sub.1 is an aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic or heterocyclic-aliphatic radical, R.sub.2 is hydrogen or an aliphatic radical and Ph is a 1,2-phenylene group containing the radical R.sub.1 --C(.dbd.O)--, with the proviso that R.sub.1 contains at least 2 carbon atoms if Ph is otherwise unsubstituted, R.sub.2 is ethyl and R is acetoxymethyl, and salts of such compounds having salt-forming properties, are useful as anti-allergic agents.

Abstract: Compounds of the class of (2-benzofuranyl)-1,2,3,6-tetrahydropyridines and (2-benzofuranyl)-piperidines which at the ring nitrogen atom are unsubstituted or substituted by a substituent of the class of certain aliphatic, cycloaliphatic and araliphatic radicals, and their pharmaceutically acceptable acid addition salts have valuable pharmacological properties. In particular, they inhibit monoamine oxidase and antagonize the action of tetrabenazine. They are useful as active ingredients for therapeutic compositions for the treatment of mental depression. Specific embodiments are 4-(2-benzofuranyl)-piperidine, 2-(5,6-dimethyl-2-benzofuranyl)-piperidine and their hydrochlorides.