WHEREIN A IS 1 OR 2, B IS 3 WHEN A IS 1 AND IS FROM 3 TO 5 WHEN A IS 2, X IS HALOGEN OF ATOMIC NUMBER FROM 17 TO 35 WITH AT LEAST ONE X BEING BONDED TO THE CARBON ATOM WHICH IS BONDED TO THE SULFUR ATOM, Y IS HALOGEN OF ATOMIC NUMBER FROM 17 O 35 OR NITRO IN POSITION 4 TO 6 OF THE INDAZOLE NUCLEUS AND N IS AN INTEGER FROM 0 TO 1. THESE COMPOUNDS ARE FUNGICIDAL AND BACTERICIDAL.
Abstract:
DI- AND TRI-ARYLPYRAZOLINE SULPHONIC ACID ESTERS ARE DESCRIBED WHICH HAVE UNEXPECTEDLY A VERY GOOD AFFINITY TO CELLULOSE ESTER FIBERS AND OPTICALLY BRIGHTEN THESE FIBERS IN PURE WHITE, FREE FROM UNDESIRABLE GREENISH OR GREENISHBLUE HUES EVEN WHEN APPLIED IN HIGHER CONCENTRATIONS; COMPOSITIONS CONTAINING SUCH NOVEL ESTERS AS WELL AS OTHER SUBSTANCES, ESPECIALLY DETERGENTS, ARE ALSO DESCRIBED; AND A PROCESS FOR OPTICALLY BRIGHTENING CELLULOSE ESTER AND PARTICULARLY CELLULOSE ACETATE FIBERS IS ALSO DISCLOSED.
Abstract:
Pyrazole-3-carboxylic acids, useful as complement inhibitors, are prepared by the alkaline hydrolysis of pyrazolo(1,5c)quinazolin-5(6H)-one-2-carboxylic acids or esters thereof.
Abstract:
IN WHICH Hal represents a halogen, R represents an alkyl group containing 1 to 5 carbon atoms either unsubstituted or substituted by a non-ionic and non-chromophoric -chromophoric group, each of the substituents R1, R2 or R3, which are the same or different, representing a hydrogen or halogen atom, or an alkyl group comprising from 1 to 3 carbon atoms, or an aryl group; processes for their preparation and their use as fluorencent brightening agents for polyester fibres.
Abstract:
This chemical process invention provides 3,4,5-tribromopyrazole by direct tribromination of pyrazole in an aqueous reaction medium with alkali metal hydroxide. It further provides Nalkylation in the same aqueous alkaline medium to obtain 1(substituted-hydrocarbyl)-3,4,5-tribromopyrazoles useful as herbicides.
Abstract:
Indazoles that have the structural formula
WHEREIN X represents halogen, nitro, -SO2R, cyano, acoyl, acoylamino, aroylamino, alkyl, alkoxy, carboalkoxy, -COR, -CHO, or trihalomethyl; R represents alkylamino, hydroxy, halogen, alkyl, haloalkyl, phenyl, or substituted phenyl wherein the substituent is halogen, alkyl, or nitro; and n represents a number in the range of 1 to 4 are prepared by diazotizing the corresponding substituted o-toluidine in an aqueous mineral acid medium and adding the resulting diazonium salt solution to an aqueous solution containing basic anions, which is maintained at a pH of 4 to 10 and at a temperature of about 10*C. to 100*C. during the addition of the diazonium salt solution, and isolating the resulting indazole.