129-37-3

Basic information

• Product Name: 9,10-dihydro-8-nitro-9,10-dioxoanthracene-1-sulphonic acid
• Synonyms: 9,10-dihydro-8-nitro-9,10-dioxoanthracene-1-sulphonic acid;8-nitro-9,10-dioxo-9,10-dihydroanthracene-1-sulfonic acid;9,10-Dihydro-8-nitro-9,10-dioxo-1-anthracenesulfonic acid;8-nitro-9,10-dioxo-anthracene-1-sulfonic acid;8-nitro-9,10-dioxoanthracene-1-sulfonic acid;9,10-diketo-8-nitro-anthracene-1-sulfonic acid
• CAS NO: 129-37-3
• Molecular Formula: C₁₄H₇NO₇S
• Molecular Weight: 333.27288
• EINECS: 204-942-5
• Mol File: 129-37-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.72g/cm³
• Refractive Index: 1.705
• CAS DataBase Reference: 9,10-dihydro-8-nitro-9,10-dioxoanthracene-1-sulphonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-dihydro-8-nitro-9,10-dioxoanthracene-1-sulphonic acid(129-37-3)
• EPA Substance Registry System: 9,10-dihydro-8-nitro-9,10-dioxoanthracene-1-sulphonic acid(129-37-3)

Safety Data

• Hazardous Substances Data: 129-37-3(Hazardous Substances Data)

Usage

General Description

9,10-dihydro-8-nitro-9,10-dioxoanthracene-1-sulphonic acid is a chemical compound with the molecular formula C14H9NO7S. It is a synthetic derivative of anthracene and is commonly used in the production of dyes and pigments. 9,10-dihydro-8-nitro-9,10-dioxoanthracene-1-sulphonic acid is a sulfonic acid, which means it contains a sulfur atom bonded to three oxygen atoms and is highly water-soluble. It is often used in the manufacturing of acid dyes, which are commonly applied to wool and silk fabrics. The presence of the nitro group in the molecule gives it a yellow to red color, making it useful for creating a range of vibrant dyes. Additionally, its sulfonic acid group makes it highly reactive and easily reactive with other chemicals, allowing for the production of a variety of different dye colors.

InChI:InChI=1/C14H7NO7S/c16-13-7-3-1-5-9(15(18)19)11(7)14(17)12-8(13)4-2-6-10(12)23(20,21)22/h1-6H,(H,20,21,22)

Upstream product

• 30845-78-4 potassium 9,10-dihydro-9,10-dioxoanthracene-1-sulfonate 
• 82-49-5 1-anthraquinonesulfonic acid 

Downstream Products

• 21552-84-1 8-amino-9,10-dioxo-9,10-dihydro-anthracene-1-sulfonic acid 
• 82-48-4 1,8-anthraquinonedisulphonic acid 
• 129-38-4 8-chloro-1-nitroanthraquinone 
• 117-10-2 1,8-dihydroxy-9,10-anthracenedione 
• 82-34-8 1-nitroanthraquinone 
• 60316-43-0 1,8-bis-methylaminoanthraquinone 

Relevant articles and documents

Synthesis and cytotoxic activity of 7-oxo-7H-dibenz[f,ij]isoquinoline and 7-oxo-7H-benzo[e]perimidine derivatives

A series of 7-oxo-7H-dibenz[f,ij]isoquinoline and 7-oxo-7H-benzo[e]perimidines bearing cationic side chains were prepared from aminoanthraquinones. The perimidines were prepared from 1-aminoanthraquinone by initial condensation with urea or dimethylacetamide. A series of 2-, 4-, 8-, and 11-carboxy derivatives of the dibenzisoquinolines were prepared from aminoanthraquinonecarboxylic acids. The cationic derivatives were prepared from these via amide, amine, or methylene linkers to study the effects of side chain positioning on biological activity. Within the series of carboxamide-linked compounds, the order of increasing cytotoxicity was 8- 4- 2- 11-. The 2- and 4-carboxamides showed substantial growth delays against in vivo subcutaneous colon 38 tumors in mice, but the 11-carboxamide had curative activity in this refractory model and is being investigated further.