84-46-8

Basic information

• Product Name: 2-amino-3-chloro-anthraquinon
• Synonyms: 2-amino-3-chloro-anthraquinon;3-x-2-aa;2-amino-3-chloroanthracene-9,10-dione;2-AMINO-3-CHLORANTHRAQUINONE
• CAS NO: 84-46-8
• Molecular Formula: C₁₄H₈ClNO₂
• Molecular Weight: 257.67182
• EINECS: 201-530-7
• Mol File: 84-46-8.mol

Chemical Properties

• Boiling Point: 500.9 °C at 760 mmHg
• Flash Point: 256.7 °C
• Appearance: /
• Density: 1.486 g/cm³
• Vapor Pressure: 3.64E-10mmHg at 25°C
• Refractive Index: 1.711
• CAS DataBase Reference: 2-amino-3-chloro-anthraquinon(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-3-chloro-anthraquinon(84-46-8)
• EPA Substance Registry System: 2-amino-3-chloro-anthraquinon(84-46-8)

Safety Data

• Hazardous Substances Data: 84-46-8(Hazardous Substances Data)

Usage

Uses

Used in Textile Industry:
2-amino-3-chloro-anthraquinon is used as a dyeing agent for fabrics and fibers, providing them with a vibrant red color due to its intense pigmentation properties.
Used in Pharmaceutical and Medical Research:
2-amino-3-chloro-anthraquinon is used as a potential anti-tumor and anti-inflammatory agent, being investigated for its therapeutic properties in pharmaceutical and medical research.

InChI:InChI=1/C14H8ClNO2/c15-11-5-9-10(6-12(11)16)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,16H2

Upstream product

• 84-45-7 2,3-dichloro-anthraquinone 
• 35322-95-3 2-chloro-3-nitro-anthraquinone 
• 6374-76-1 2-amino-1,3-dichloro-anthraquinone 
• 118-04-7 NSC 74496 
• 131-09-9 2-chloroanthracene-9,10-dione 
• 7664-93-9 sulfuric acid 
• 75-44-5 phosgene 
• 117-79-3 2-aminoanthraquinone 
• 85-54-1 2-(4'-chloro-3'-nitrobenzoyl)benzoic acid 

Downstream Products

• 117-07-7 1-amino-2-chloro-9,10-anthraquinone 
• 6374-76-1 2-amino-1,3-dichloro-anthraquinone 
• 117-01-1 2-amino-1-bromo-3-chloro-anthraquinone 
• 84-42-4 N-(3-chloro-9,10-dioxo-9,10-dihydro-[2]anthryl)-acetamide 
• 78679-94-4 2-Chloro-3-phenylamino-anthraquinone 
• 78679-95-5 2-Chloro-3-diphenylamino-anthraquinone 

Relevant articles and documents

PHOTOCHEMICAL REACTION OF 9,10-ANTHRAQUINONE AND ITS DERIVATIVES WITH PYRIDINE

The previously unknown photochemical reaction of 9,10-anthraquinone with pyridine in an atmosphere of argon takes place with formation of 2-(1,2-dihydropyridino)- or 2-(1,4-dihydropyridino)-9,10-anthraquinone, which is converted by the action of alkali into 2-aminoanthraquinone.In the presence of atmospheric oxygen the reaction product after treatment whith alkali is 1-aminoanthraquinone in addition to 2-aminoanthraquinone.The 1- and 2-methoxyanthraquinones and chloroanthraquinones react with pyridine in the light and form, after treatment with alkali, substituted aminoanthraquinones.