GB277670A - Manufacture of benzanthrone-carboxylic acids - Google Patents
Manufacture of benzanthrone-carboxylic acidsInfo
- Publication number
- GB277670A GB277670A GB24216/27A GB2421627A GB277670A GB 277670 A GB277670 A GB 277670A GB 24216/27 A GB24216/27 A GB 24216/27A GB 2421627 A GB2421627 A GB 2421627A GB 277670 A GB277670 A GB 277670A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzanthrone
- carboxylic acids
- manufacture
- carboxylic acid
- methylbenzanthrones
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/02—Benzathrones
- C09B3/06—Preparation from starting materials already containing the benzanthrone nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
277,670. I. G. Farbenindustrie Akt.- Ges. Sept. 20, 1926, [Convention date]. Benzanthrone carboxylic acids are obtained by oxidizing alkylbenzanthrones in presence of alkaline agents such as caustic alkali. The reaction is applicable whether the alkyl group is in the benzene ring or in the anthraquinone nucleus of the benzanthrone molecule. According to examples, benzanthrone-Bz1-or-Bz2-carboxylic acid and benzanthrone-2-carboxylic acid are obtained by heating the corresponding methylbenzanthrones with powdered caustic potash and nitrobenzene. Specifications 268,830 and 273,774 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE277670X | 1926-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB277670A true GB277670A (en) | 1928-11-01 |
Family
ID=6028367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24216/27A Expired GB277670A (en) | 1926-09-20 | 1927-09-14 | Manufacture of benzanthrone-carboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB277670A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4812393A (en) * | 1986-01-31 | 1989-03-14 | Eastman Kodak Company | Fluorescent dyes and biological and analytical uses thereof |
US4927927A (en) * | 1986-01-31 | 1990-05-22 | Eastman Kodak Company | Fluorescent dyes and biological and analytical uses thereof |
-
1927
- 1927-09-14 GB GB24216/27A patent/GB277670A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4812393A (en) * | 1986-01-31 | 1989-03-14 | Eastman Kodak Company | Fluorescent dyes and biological and analytical uses thereof |
US4927927A (en) * | 1986-01-31 | 1990-05-22 | Eastman Kodak Company | Fluorescent dyes and biological and analytical uses thereof |
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