Abstract:
ACID HALIDES ARE PREPARED BY REACTING PARAFFINS WITH CARBON MONOXIDE AND HALOHYDROCARBONS; USE OF THE HALOHYDROCARBON ALLOWS FORMATION OF ACID HALIDE IN PREFERENCE TO HALIDE; PRODUCTS ARE USEFUL AS CHEMICAL INTERMEDIATES, E.G., IN THE PREPARATION OF TEXTILE WETTING AGENTS.
Abstract:
Substantially gel-free, high molecular weight, high unsaturation copolymers of isobutylene and conjugated dienes having a number average molecular weight of at least 120,000 and a mole percent of unsaturation of at least 5 percent and the process for preparing said polymers which comprises carrying out the polymerization in a homogeneous phase, introducing the catalyst comprising an aluminum halide to the system in a soluble form and carrying the reaction out at a temperature of less than -100*C.
Abstract:
3-Halo-1,2,4 thiadiazole-5 sulfenyl halides are produced by reacting cyanodithioimidocarbonate anion with the corresponding halogen. 3-Halo-1,2,4 thiadiazole-5 sulfenyl halides are useful as pesticides and chemical intermediates. Derivatives of the 3halo-1,2,4 thiadiazole-5 sulfenyl halides include the di(3-halo1,2,4 thiadiazol-5-yl) disulfides, and are useful as pesticides, antioxidants, and U.V. stabilizers.
Abstract:
NEUTRAL S-2-HYDROCARBYLTHIOALKYL ESTERS OF THIOPHOSPHOROUS ACIDS ARE PREPARED THROUGH THE DISPLACEMENT REACTION OF A 2-HYDROCARBYL-2-HYDROCARBYLTHIOETHYL HALIDE ALONE OR IN ADMIXTURE WITH THE CORRESPONDING ISOMERIC SECONDARY HALIDE COMPOUND WITH A DIORGANO THIOPHOSPHATE, THIOPHOSPHONATE OR THIOPHOSPHINATE SALT, THE DISPLACEMENT REACTIONS ARE CONDUCTED AT MODERATE TEMPERATURES AND PRESSURE, PREFERABLY IN THE PRESSENCE OF A POLAR DILUENT. THE PERFERRED THIOPHOSPHORUS ACID AND DIALKYL MONOTHIOPHOSPHORIC ACIDS. THE PREFERRED HALIDE REACTANTS ARE 2-ALKYL-2-ALKYTHIOETHYL CHLORIDES ALONE OR IN COMBINATION WITH 1-ALKYL-2-ALKYLTHIOETHYL CHLORIDES. THE COMPOUNDS DERIVED FROM THE DISPLACEMENT REACTIONS POSSES PARTICULARLY GOOD PESTICIDAL ACTIVITY.