Abstract:
METHODS OF SELECTIVELY COMBATING AND CONTROLLING SHORTTAILED MICE USING CERTAIN (1-FLUOROACETYLAMINO-2,2,2-TRICHLORO-ETH-1-YL)-(ALKOXYTHIOCARBONYL, BENZOYL AND ALKYLPHENYL)-THIOETHERS, I.E. 1-(ALKOXYTHIOCARBONYLMERCAPTO, BENZOYLMERCAPTO AND ALKYLPHENYLMERCAPTO) - 1 - FLUOROACETYLAMINO - 2,2,2 - TRICHLORO-ETHANES, WHICH ARE KNOWN, WHICH POSSES SELECTIVE RODENTICIDAL PROPERTIES, AND WHICH MAY BE PRODUCED BY CONVENTIONAL METHODS.
Abstract:
1,232,564. Phosphoric acid esters. FARBENFABRIKEN BAYER A.G. 30 Jan., 1969 [2 Feb., 1968], No. 5213/69. Heading C2C. [Also in Division A5] Phosphoric, phosphonic or thiono-phosphoric (-phosphonic) acid esters of the general formula in which R 1 and R 3 are each a straight or branched (possibly halogen substituted) alkoxy radical with 1 to 6 carbon atoms or C 1 -C 4 alkylamino or di-C 1 -C 4 alkylamino group, R 2 and R 4 are each a C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, alkylamino, dialkylamino, alkoxy, haloalkoxy or phenyl radical, and X and Y are oxygen and/or sulphur atoms are prepared by reacting a phosphoric or thionophosphoric (-phosphonic) acid ester halide of the formula in which Hal is a halogen atom with maleic acid hydrazide in the presence of an acid-binding agent. The esters possess insecticidal and acaricidal properties.
Abstract:
1,250,820. Thionophosphonic acid esters. FARBENFABRIKEN BAYER AG. 27 March, 1969 [27 March, 1968], No. 16122/69. Heading C2P. The invention comprises compounds of the formula wherein R 1 is a C 1 -C 6 alkyl or haloalkyl radical or a phenyl, halophenyl or C 1 -C 6 alkylphenyl radical and R 2 is a C 1 -C 6 alkyl or haloalkyl radical. They may be obtained by reacting (R 2 0)(R i )P(S)Hal with maleic acid hydrazide in the presence of an acid-binding agent, e.g. an alkali metal alcoholate or carbonate, or a tertiary amine, and preferably in the presence of a solvent or diluent, e.g. a hydrocarbon, ether, ketone, low-boiling aliphatic alcohol, dimethylformamide or a nitrile. The products have insecticidal, acaricidal and rodenticidal properties and may be admixed with an inert solid or liquid carrier or diluent and/or surface active agent to form conventional formulations.
Abstract:
Compositions and methods of using phosphoryl-, phosphonyl-, thionophosphoryl- and thionophosphonyl- - Alpha -oximinoarylacetic acid nitriles which possess pesticidal, especially insecticidal and/or acaricidal, properties, and which may be produced by reacting the corresponding phosphorus acid ester halide with the corresponding Alpha -oximino-arylacetic acid nitrile.
Abstract:
Phosphonic and thiphosphonic acid esters of 2-hydroxy 3,5,6-trichloropyridine, R1 = alkyl-R2 = alkyl-, phenyl-X = O or S Insecticides, acaricides. Potassium carbonate is added to a suspension of 2-hydroxy 3,5,6-trichloropyridine in acetonitrile and the mixture warmed to 60 deg. C for 1/2 hour. When the temperature has cooled to 50 deg. C methylthiono-phosphonic O-ethyl chloride is added dropwise. The mixture is heated for 4 hrs. at 70 deg. C and the stirring is continued for another 3 hrs. After filtration of the separated sodium chloride the filtrate is extracted with benzene. The benzene solution is washed with water, dried and the solvent distilled off. Recrystallisation of the residue from ethanol yields O-ethyl O-(3,5,6-trichloropyridyl-2) methylthiono-phosphonate.
Abstract:
O-alkyl-O-pyrazolyl-phosphoric, phosphonic, thionophosphoric and thionophosphonic acid esters, i.e., (alkyl, phenyl and O-alkyl)O-alkyl-O-(1-((alkyl, phenyl and O-alkyl)-O-alkyl-(phosphoryl, phosphonyl, thionophosphoryl and thionophosphonyl))-5-methylpyrazol-3-yl)-phosphoric, phosphonic, thionophosphoric and thionophosphonic acid esters, which possess arthropodicidal, especially acaricidal and insecticidal, properties, and which may be produced by conventional methods.
Abstract:
1-FLUOROACETYLAMINO-2,2,2-TRICHLORO-EHTYL UREAS, I.E. N(1-FLUOROACETYLAMINO-2,2,2-TRICHLORO-ETH-1-YL)-(H(ALKYL, PHENYL, ALKOXYPHENYL AND CHLORO-SUBSTITUTED PHENYL)UREAS, WHICH POSSESS SELECTIBE RODENTICIDAL PROPERITES, AND WHICH MAY BE PRODUCED BY CONVENTIONAL METHODS.