in which EACH INDEPENDENTLY STANDS FOR A HALOGEN ATOM, ALKYL WITH 1-4 CARBON ATOMS OR ALKOXY WITH 1-4 CARBON ATOMS, N STANDS FOR 0, 1 OR 2, R stands for alkyl with 1-12 carbon atoms, R'' and R'''' each stands independently for a hydrogen atom or alkyl with 1-4 carbon atoms, and R'''''' stands for a hydrogen atom, alkyl with 1 or 2 carbon atoms (which may carry at least one substituent selected from halogen, cyano, alkoxy with up to 4 carbon atoms and alkoxycarbonyl with up to 5 carbon atoms), alkyl with 3 to 18 carbon atoms (which carries at least one substituent selected from halogen, cyano, alkoxy with up to 4 carbon atoms and alkoxycarbonyl with up to 5 carbon atoms), cycloalkyl with 5 to 8 ring carbon atoms, aralkyl (the aryl moiety of which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), phenyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), acyl with up to 18 carbon atoms (which may be substituted by halogen and/or lower alkyl), aroyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), alkylsulfonyl with up to 18 carbon atoms, arylsulfonyl (which may carry at least one substituent selected from halogen, amino, lower alkyl and lower alkoxy) or dialkylamino with up to 4 carbon atoms, possess fungicidal properties.
Abstract:
The invention comprises reactive dyes of formula wherein F is an organic dye radical, Q is an -SO2-NR1-, -NR1-SO2-, -CO-NR1- or -NR1-CO- bridge member, R1 being hydrogen or C1-C5 alkyl, A is a six-membered carbocyclic ring, X is a hydrogen or chlorine atom or a methyl group, Y1 is a chlorine atom or an alkylsulphonyl or arylsulphonyl radical, Z is -O-, -S- or =N-CH3, m is 1 or 2 and n is 1, 2 or 3. The dyes may be prepared by condensing a dye or a diazo or coupling component containing an amino or amide group with a compound of formula wherein W is a carboxylic or sulphonic acid halide group and if an azo dye component is used forming the dye by the usual coupling reaction. Conversely dyestuff acid halides may be condensed with compounds of the above formula wherein W is an amino group. The dyes may be used to colour amide or hydroxyl group-containing fibres by the usual reactive dye processes. The preparation of monoazo, metallized azo, phthalocyanine and anthraquinone dyes is described in examples.
Abstract:
1-TERT.-BUTYL-THIOSEMICARBAZIDE COMPOUNDS OF THE FORMULA
wherein R and R'' are hydrogen, aliphatic, cycloaliphatic or aromatic hydrocarbyl (optionally substituted) or where an R and R'' together with the nitrogen linking them can form a heterocyclic system ARE PRODUCED BY REACTING A THIOSEMICARBAZIDE OF THE FORMULA
with tertiary butanol in the presence of a dehydrating agent at a temperature of from 0* to 100*C.
Abstract:
B-ALKOXY-ACRYLIC ACID AMIDES, I.E. B-(ALKOXY, CYCLOALKOXY, ALKYL-CYCLOALKOXY AND ALKYL-CYCLOALKYL-ALKOXY) ACRYLIC ACID N-(ALKYL, ALKENYL, CYCLOALKY, ALKYL-CYCLOAKYL, PHENYL-ALKYL AND CHLORO-PHENYL-ALKYL)-N-(UNSUBSTITUTED AND OPTIONALLY ALKYL, ALKENYL, CYCLOALKYL AND PHENYLALKYL)-AMIDES, WHICH POSSESS PESTICIDAL, ESPECIALLY INSECTICIDAL AND ACARICIDAL, PROPERTIES AND WHICH MAY BE PRODUCED BY REACTING THE CORRESPONDING B-ALKOXY-ACRILIC ACID CHLORIDE WITH THE APPROPRIATE AMINE.
in which each X independently stands for a halogen atom, alkyl with 1-4 carbon atoms or alkoxy with 1-4 carbon atoms, n stands for 0, 1 or 2, R stands for alkyl with 1-12 carbon atoms, R'' and R'''' each stands independently for a hydrogen atom or alkyl with 1-4 carbon atoms, and R'''''' stands for a hydrogen atom, alkyl with 1 or 2 carbon atoms (which may carry at least one substituent selected from halogen, cyano, alkoxy with up to 4 carbon atoms and alkoxycarbonyl with up to 5 carbon atoms), alkyl with 3 to 18 carbon atoms (which carries at least one substituent selected from halogen, cyano, alkoxy with up to 4 carbon atoms and alkoxycarbonyl with up to 5 carbon atoms), cycloalkyl with 5 to 8 ring carbon atoms, aralkyl (the aryl moiety of which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), phenyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), acyl with up to 18 carbon atoms (which may be substituted by halogen and/or lower alkyl), aroyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), alkylsulfonyl with up to 18 carbon atoms, arylsufonyl (which may carry at least one substituent selected from halogen, amino, lower alkyl and lower alkoxy) or dialkylamino with up to 4 carbon atoms, which possess fungicidial properties and which may be produced by conventional methods.