Abstract: Novel dihydroisoxazole compounds are disclosed having activity against parasitic worms and showing little or no toxicity to the host animal. These compounds are 3-chloro-4-dialkylaminophthaloylamino-4,5-dihydroisoxazoles and 3-dialkylamino-4-dialkylaminophthaloylamino-4,5-dihydroisoxazoles. A process for making these compounds and a method of administering them to infested animals is also disclosed.

Abstract: Novel phthalamide compounds are disclosed having activity against a broad spectrum of parasitic worms and showing no toxicity to the host animal. These compounds are N-(3-chloro-4,5-dihydroisoxazol-4-yl)-N'-(substituted)phthalamides. A process for making these compounds and a method of administering them to animals are also disclosed.

Abstract: A novel tolylthioisoxazole compound is disclosed having activity against the pinworms S. obvelata and A. tetraptera. A process for making these compounds and a method of administering it to infested animals is also disclosed.

Abstract: Novel dihydroisoxazole compounds are disclosed having activity against parasitic worms and showing little or no toxicity to the host animal. These compounds are 3-chloro-4-dialkylaminophthaloylamino-4,5-dihydroisoxazoles and 3-dialkylamino-4-dialkylaminophthaloylamino-4,5-dihydroisoxazoles. A process for making these compounds and a method of administering them to infested animals is also disclosed.

Abstract: Certain phenylthioalkylamines and amides thereof are antifungal or antibacterial agents, or both, and provide a method of controlling the growth of these microorganisms.

Abstract: Certain phenylthioalkylamines and amides thereof are antifungal or antibacterial agents, or both, and provide a method of controlling the growth of these microorganisms.

Abstract: A method of controlling the growth of microorganisms by using a compound represented by the formula ##STR1## wherein R is hydrogen or methyl, R.sup.1 is hydrogen, methyl or ethyl, or R and R.sup.1 can collectively be a cyclic alkyl group of 5 carbon atoms.

Abstract: The product prepared by the process consisting of the steps of (a) reacting a nitroalcohol of the formula ##STR1## where R and R.sup.1 can be hydrogen, methyl, ethyl or hydroxymethyl in about a 1:1 mole ratio with an alkylamine represented by the formula R.sup.2 NH.sub.2 where R.sup.2 is alkyl of from 1 to 4 or more carbon atoms or phenyl, benzyl, toluyl, or xylyl at about 50.degree.-70.degree. thereby effecting formation of a nitroalkylamine; (b) reacting the nitroalkylamine with nitrous acid at about 0.degree.-5.degree., thereby forming a nitroso compound; and (c) reducing the nitroso compound.

Abstract: The product prepared by the process consisting of the steps of (a) reacting a nitroalcohol of the formula ##STR1## where R and R.sup.1 can be hydrogen, methyl, ethyl or hydroxymethyl in about a 1:1 mole ratio with an alkylamine represented by the formula R.sup.2 NH.sub.2 where R.sup.2 is alkyl of from 1 to 4 or more carbon atoms or phenyl, benzyl, toluyl, or xylyl at about 50.degree.-70.degree. thereby effecting formation of a nitroalkylamine; (b) reacting the nitroalkylamine with nitrous acid at about 0.degree.-5.degree., thereby forming a nitroso compound; and (c) reducing the nitroso compound.

Abstract: Tranquilizing agents for warm-blooded animals corresponding to the formula ##EQU1## where n can be 1 or 2; Y can be ##EQU2## where R.sup.2 can be hydrogen or an alkyl, alkenyl, alkoxy, phenyl or methoxyphenyl radical. Z can be thienyl, furyl, phenyl; or mono-, di-, or trimethoxyphenyl; mono-, or dichlorophenyl, or dichlorophenoxy. R and R.sup.1 can be hydrogen, methyl, or ethyl and can be the same or different.