序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
221 PLEOCHROIC DYES SUITABLE FOR USE IN SOLUTION WITH LIQUID CRYSTAL MATERIALS FOR ELECTRO-OPTIC DEVICE APPLICANTS GB7840535 1978-10-13 GB2011940B 1982-10-27
222 Anthrachinonazoverbindungen, process for their manufacture and their use DE3106358 1981-02-20 DE3106358A1 1982-09-09 ROLF MEINHARD DR; NEEFF RUETGER DR; MUELLER WALTER
223 MONOAZO PIGMENTS AND PROCESSES FOR THEIR MANUFACTURE GB7906186 1979-02-21 GB2015015B 1982-06-30
224 FR2418258B1 - FR7904642 1979-02-23 FR2418258B1 1982-05-14
225 pigments DE3024957 1980-07-02 DE3024957A1 1982-02-11 DIMROTH PETER DIPL CHEM DR; LOTSCH WOLFGANG DIPL CHEM DR
226 Pleochroic anthraquinone dye, process for its production and use of the dye DE3007198 1980-02-26 DE3007198A1 1981-09-03 MOELLER ALEXANDER DIPL CHEM; SCHEROWSKY GUENTHER DR
227 Azo compounds GB7906756 1979-02-26 GB2035352A 1980-06-18
Novel azo compounds of the general formula:- (E)n@(A)n@ - (R1)n@ - N = N - BAL where A is a charged group which may be positively or negatively charged, E is a counter ion which carries a charge of opposite sign to that carried by A, BAL represents a ballasting group attached to the azo group via an aromatic or heterocyclic ring which may be further substituted, and R1 is an optionally substituted aromatic or heterocyclic group, and n1 is 1 or 2, n2 is 1 or 2 and n3 is 0 or 1 are used in diffusion transfer colour photographic materials. Example: A dyestuff of the formula:-
228 Anthraquinone-azo compounds, their preparation and their use as dyestuffs GB7931973 1979-09-14 GB2032941A 1980-05-14
The invention provides water- soluble anthraquinone-azo dyestuffs of the general formula in which R1 represents a hydrogen atom or a sulphonic acid group, and the two R1s are not both hydrogen, K represents the radical of a coupling component and Z represents a fibre- reactive group which is linked to a carbocyclic aromatic nucleus of the coupling component, n being 1 or 2. The compounds may also be in the form of their salts. The compounds, preferably in the form of alkali metal salts, are useful for dyeing and printing fibre materials containing carboxamide groups, e.g. silk, wool and other animal hairs, polyamide and polyurethane fibres, and fibre materials containing hydroxy groups, e.g. cotton, linen and viscose rayon. Green to olive-green, blue and grey dyeings are obtained having good fastness to wet processing and very good fastness to light. The invention also provides intermediates for these dyestuffs in which the Zn group is replaced by an NHR group in which R represents a hydrogen atom or a lower alkyl group or a cyano-lower alkyl group.
229 DD20847678 1978-10-16 DD141321A5 1980-04-23 CONSTANT JENNIFER; PELLATT MARTIN G; ROE IAIN H
230 Anthraquinone-azo compounds, their preparation and use as dyestuffs DE2840119 1978-09-15 DE2840119A1 1980-03-27 FUCHS HERMANN DIPL CHEM DR
231 IT2613579 1979-09-28 IT7926135A0 1979-09-28 HARTMUT KANTER
232 mono-azo pigments, anthraquinone FR7904642 1979-02-23 FR2418258A1 1979-09-21
<P>Composés azoïques anthraquinoniques. Ils répondent à la formule :</P>
233 Azo compounds (hydrazo) anthraquinone and their method of preparing FR7904908 1979-02-26 FR2418256A1 1979-09-21
<P>Nouveaux composés azo(hydrazo)-anthraquinone. </P><P>Les nouveaux composés répondent à la formule générale :</P>
234 ANTHRAQUINONES GB7906760 1979-02-26 GB2016030A 1979-09-19
235 IT4812279 1979-02-26 IT7948122A0 1979-02-26
236 Water-insoluble azo dyes and processes for their preparation, as well as their coupling components and methods for making the coupling components DE2708418 1977-02-26 DE2708418A1 1978-08-31 HEINRICH ERNST DR; PIESCH STEFFEN DR; TAPPE HORST DR; RIBKA JOACHIM DR
237 Heterocyclic compounds DE2644265 1976-09-30 DE2644265A1 1978-04-06 ROLF MEINHARD DR; NEEFF RUETGER DR; MUELLER WALTER
238 FR2224521B3 - FR7410847 1974-03-28 FR2224521B3 1977-01-21
239 DD17068573 1973-05-08 DD104545A5 1974-03-12
240 POSTOPEK ZA PRIPRAVO NOVIH 9,10 - STEROIDOV YU15468 1968-01-22 YU31939B 1974-02-28
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