24929-02-0

Basic information

• Product Name: 1-amino-9,10-dihydro-4-hydroxy-9,10-dioxoanthracene-2-sulphonic acid
• Synonyms: 1-amino-9,10-dihydro-4-hydroxy-9,10-dioxoanthracene-2-sulphonic acid;1-Amino-4-hydroxy-9,10-dihydro-9,10-dioxoanthracene-2-sulfonic acid;1-Amino-9,10-dihydro-4-hydroxy-9,10-dioxo-2-anthracenesulfonic acid;Einecs 246-537-6
• CAS NO: 24929-02-0
• Molecular Formula: C₁₄H₉NO₆S
• Molecular Weight: 319.28936
• EINECS: 246-537-6
• Mol File: 24929-02-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.749g/cm³
• Refractive Index: 1.75
• CAS DataBase Reference: 1-amino-9,10-dihydro-4-hydroxy-9,10-dioxoanthracene-2-sulphonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-amino-9,10-dihydro-4-hydroxy-9,10-dioxoanthracene-2-sulphonic acid(24929-02-0)
• EPA Substance Registry System: 1-amino-9,10-dihydro-4-hydroxy-9,10-dioxoanthracene-2-sulphonic acid(24929-02-0)

Safety Data

• Hazardous Substances Data: 24929-02-0(Hazardous Substances Data)

Usage

Derivative of

Anthraquinone

Functional groups

a. Hydroxy group
b. Keto group
c. Amino group
d. Sulphonic acid group

Use as a pH indicator

Yes

Color in acidic conditions

Orange to red

Color in alkaline conditions

Yellow to green

Applications

a. Dyeing and textile industry
b. Biochemical research
c. Medical research

InChI:InChI=1/C14H9NO6S/c15-12-9(22(19,20)21)5-8(16)10-11(12)14(18)7-4-2-1-3-6(7)13(10)17/h1-5,16H,15H2,(H,19,20,21)

Upstream product

• 4319-49-7 1-aminomorpholine 
• 116-81-4 1-amino-4-bromo-9,10-dioxoanthracene-2-sulphonic acid 
• 617-89-0 furan-2-ylmethanamine 
• 75-31-0 isopropylamine 
• 1003-03-8 Cyclopentamine 
• 83759-22-2 1-amino-4-hydroxyanthraquinone-3-sulfonic acid 
• 116-85-8 4-hydroxy-1-aminoanthraquinone 
• 88-63-1 2,4-Diaminobenzenesulfonic acid 
• 116-82-5 1-amino-2-bromo-4-hydroxyanthraquinone 
• 6258-06-6 sodium 1-amino-4-bromoanthraquinone-2-sulfonate 
• 122-80-5 N-acetyl-p-phenylenediamine 
• 98416-38-7 4,9-Diamino-1,10-dioxo-1,10-dihydro-anthracene-2-sulfonic acid; compound with ammonia 

Downstream Products

• 97404-77-8 1-amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracene-2,3-dicarbonitrile 
• 38924-11-7 1-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-3-phenyl-urea 

Relevant articles and documents

Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists

A library of anilinoanthraquinone derivatives was synthesized by parallel Ullmann coupling reaction of bromaminic acid with aniline derivatives in solution using a compact parallel synthesizer. The products were purified by HPLC and evaluated as antagonists at mouse and human P2Y2 receptors. 4-Phenylamino-substituted 1-amino-2-sulfoanthraquinones, for example, 1-amino-4-(2-methoxyphenyl)-2-sulfoanthraquinone (PSB-716), were potent P2Y2 antagonists with IC50 values in the low micromolar range.

REACTION OF ISOMERIC 1,4-AMINOHYDROXYANTHRAQUINONE-2-SULFONIC ACIDS WITH AMMONIA

-