Abstract:
Novel 2,4-bis-(trifluoromethyl)-6-nitrophenol compounds of the formula
IN WHICH X is hydrogen; M; HNR 1R2R3; -COR4; -COOR5; N,Ndimethylaminocarbonyl; -SO2R6 or -CO-NH-R7; M is an equivalent of an alkali metal or alkaline earth metal, R1, R2 and R3 (individually) are hydrogen, alkyl, alkoxyalkyl, alkenyl, hydroxyalkyl, cycloalkyl, phenyalkyl, phenyl or substituted phenyl, R4 and R5 individually are alkyl, substituted alkyl, alkenyl, phenyl or substituted phenyl, R6 is alkyl, substituted alkyl, phenyl, substituted phenyl or dimethylamino, and R is alkyl, alkenyl, cycloalkyl, phenyl or substituted phenyl; ARE OUTSTANDINGLY EFFECTIVE SELECTIVE HERBICIDES.
Abstract:
NOVEL 3-AMINOBENZOTHIOPHENES ARE OBTAINED BY A PROCESS WHEREIN A MERCAPTOMETHYL COMPOUND IS REACTED IN THE PRESENCE OF A BASE WITH BENZONITRILE DERIVATIVES. THE NOVEL COMPOUNDS, I.E., 2-CARBETHOXY-3-AMINO-5,7DINITROBENZOTHIOPHENE, CAN BE USED FOR DYING PLASTICS AS POLYVINYL CHLORIDE.
Abstract:
REACTING HALOGENATED BENZENES CONTAINING AT LEAST TWO DICHLOROMETHYL GROUPS WITH MONOHYDRIC OR POLYHYDRIC ALCOHOLS TO OBTAIN MONOALKOXYBENZALDEHYDE ACETALS WHICH ARE USEFUL AS HERBICIDES.
Abstract:
Novel benzthiazole-N-oxides are obtainable by the reaction of halogenonitrobenzenes additionally activated by one or more electronegative substituents with mercaptomethyl compounds in an inert solvant in the presence of a base in the temperature range of from 20* to 160* C. The new benzthiazole-N-oxides are suitable for use as colored pigments e.g. for dyeing plastics.
Abstract:
NOVEL BENZOLTHIOPHENE DERIVATIVES ARE OBTAINED BY REACTING AN AROMATIC O-CHLORO-ALDEHYDE IN THE PRESENCE OF AN ACID BINDING AGENT WITH A MERCAPTOMETHYL COMPOUND. THE NEW COMPOUNDS OBTAINABLE ACCORDING TO THIS PROCESS ARE USEFUL AS LIGHT PROTECTIVE AGENTS FOR POLYVINYL CHLORIDE.
Abstract:
Novel 6-nitroaniline compounds of the formula
IN WHICH R1 is hydrogen, substituted or unsubstituted alkyl or aryl, or cycloalkyl; R2 is hydrogen, alkyl or alkenyl; and R1 and R2 together can form a heterocycle; AND OF X and Y one is cyano and the other trifluoromethyl ARE HERBICIDES HAVING OUTSTANDING ACTIVITY AND SELECTIVITY.
Abstract:
A process for preparation of 4-aminoquinazolines and novel 4aminoquinazolines. In the process a benzonitrile derivative substituted in the 2-position by a halogen atom or alkoxy, alkylthio, aryloxy or arylthio group and in the 3- and/or 5position by an electronegative radical, is reacted with a compound corresponding to the general formula IN WHICH R represents a hydrogen atom, a hydrocarbon radical, an amino group, mono- or di-substituted amino group or a substituted sulphydryl group, in an inert solvent.
Abstract:
PRODUCTION OF AROMATIC LACTONES BY HYDROLYZING AN AROMATIC COMPOUND, E.G. BENZENE, NAPHTHALENE AND DIPHENYLDICHLORO-METHANE COMPOUNDS, CONTAINING AT LEAST TWO ORTHDICHLOROMETHYL GROUPS, WITH THE REMAINDER OF THE NUCLEAR POSITIONS THEREOF HAVING ALL OF THE CORRESPONDING HYDROGEN ATOMS THEREAT SUBSTITUTED BY CHLORO AND/OR DICHLOROMETHYL SUBSTITUENTS, WITH A HYDROLYZING AGENT, E.G. AT LEAST ABOUT 75% SULFURIC ACID OR OLEUM AT ABOUT 80200*C., SUCH AROMATIC LACTONES BEING USABLE AS INTERMEDIATES FOR REACTION WITH PRIMARY AND SECONDARY AMINES, I.E. TO EXCHANGE ONE OR MORE CHLORO SUBSTITUTENTS THEREWITH, TO FORM FLUORESCENT DYES OR OPTICAL BRIGHTENERS, THOSE AROMATIC LACTONES IN WHICH AT LEAST ONE SUBSTITUENT IS OTHER THAN CHLORO BEING NEW.