GB2014178A - 6/7-Halogenoanthraquinone compounds, and the production and use thereof - Google Patents

6/7-Halogenoanthraquinone compounds, and the production and use thereof

Info

Publication number
GB2014178A
GB2014178A GB7902500A GB7902500A GB2014178A GB 2014178 A GB2014178 A GB 2014178A GB 7902500 A GB7902500 A GB 7902500A GB 7902500 A GB7902500 A GB 7902500A GB 2014178 A GB2014178 A GB 2014178A
Authority
GB
United Kingdom
Prior art keywords
halogenoanthraquinone
compounds
production
image
halogen atom
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB7902500A
Other versions
GB2014178B (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of GB2014178A publication Critical patent/GB2014178A/en
Application granted granted Critical
Publication of GB2014178B publication Critical patent/GB2014178B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16Amino-anthraquinones
    • C09B1/20Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16Amino-anthraquinones
    • C09B1/20Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • C09B1/34Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
    • C09B1/346Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in a substituent
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/51N-substituted amino-hydroxy anthraquinone
    • C09B1/514N-aryl derivatives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/52Amino-hydroxy-anthraquinones; Ethers and esters thereof sulfonated
    • C09B1/523N-substituted amino and hydroxy anthraquinone
    • C09B1/525N-aryl derivatives

Abstract

6/7-Halogenoanthraquinone compounds or mixtures thereof of the formula <IMAGE> in which X is a halogen atom which is in the 6- or 7-position of the anthraquinone molecule. R is the <IMAGE> wherein the phenyl group A is further substituted at least in the X2 position, and/or B can be further substituted once or several times and independently of A, and at least one X1 is a halogen atom and the other is hydrogen or a halogen atom. <IMAGE>
GB7902500A 1978-01-25 1979-01-24 Halogenoantyraquinone compounds and the production and usethereof Expired GB2014178B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH80678 1978-01-25

Publications (2)

Publication Number Publication Date
GB2014178A true GB2014178A (en) 1979-08-22
GB2014178B GB2014178B (en) 1982-07-21

Family

ID=4195618

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7902500A Expired GB2014178B (en) 1978-01-25 1979-01-24 Halogenoantyraquinone compounds and the production and usethereof

Country Status (4)

Country Link
JP (1) JPS54110230A (en)
DE (1) DE2902485A1 (en)
FR (1) FR2415620A1 (en)
GB (1) GB2014178B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2423471A1 (en) * 1978-04-21 1979-11-16 Ciba Geigy Ag 6/7-HALOGENO-ANTHRAQUINONIC COMPOUNDS, THEIR PREPARATION PROCESS AND THEIR USE AS ACIDIC OR DISPERSED COLORS
US4661293A (en) * 1983-12-01 1987-04-28 The Clorox Company Method for preparing 1,4-diaminoanthraquinones and intermediates thereof
US4746461A (en) * 1986-05-23 1988-05-24 The Clorox Company Method for preparing 1,4-diaminoanthraquinones and intermediates thereof
EP1127922A1 (en) * 1999-12-29 2001-08-29 Ciba SC Holding AG Pigment dyes for the bulk dyeing of synthetic materials
US6485559B2 (en) 1999-12-29 2002-11-26 Ciba Specialty Chemicals Corporation Pigment colorants for the mass-coloring of synthetic materials

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2377145A (en) * 1940-12-13 1945-05-29 Sandoz Ag Dyestuffs of the anthraquinone series and a process for their manufacture
FR1410542A (en) * 1963-09-24 1965-09-10 Sandoz Sa Water-soluble amino-anthraquinone dyes, their manufacture and applications
NL130102C (en) * 1964-12-21 1970-06-15

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2423471A1 (en) * 1978-04-21 1979-11-16 Ciba Geigy Ag 6/7-HALOGENO-ANTHRAQUINONIC COMPOUNDS, THEIR PREPARATION PROCESS AND THEIR USE AS ACIDIC OR DISPERSED COLORS
US4661293A (en) * 1983-12-01 1987-04-28 The Clorox Company Method for preparing 1,4-diaminoanthraquinones and intermediates thereof
US4746461A (en) * 1986-05-23 1988-05-24 The Clorox Company Method for preparing 1,4-diaminoanthraquinones and intermediates thereof
EP1127922A1 (en) * 1999-12-29 2001-08-29 Ciba SC Holding AG Pigment dyes for the bulk dyeing of synthetic materials
US6485559B2 (en) 1999-12-29 2002-11-26 Ciba Specialty Chemicals Corporation Pigment colorants for the mass-coloring of synthetic materials

Also Published As

Publication number Publication date
DE2902485A1 (en) 1979-07-26
FR2415620A1 (en) 1979-08-24
GB2014178B (en) 1982-07-21
JPS54110230A (en) 1979-08-29

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Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee