10165-33-0

Basic information

• Product Name: 1-amino-2-methoxyanthracene-9,10-dione
• Synonyms: 1-amino-2-methoxyanthraquinone
• CAS NO: 10165-33-0
• Molecular Formula: C₁₅H₁₁NO₃
• Molecular Weight: 253.2527
• Mol File: 10165-33-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 221.5°C
• Boiling Point: 502°C at 760 mmHg
• Flash Point: 274.9°C
• Density: 1.366g/cm³
• Vapor Pressure: 3.3E-10mmHg at 25°C
• Refractive Index: 1.674
• CAS DataBase Reference: 1-amino-2-methoxyanthracene-9,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-amino-2-methoxyanthracene-9,10-dione(10165-33-0)
• EPA Substance Registry System: 1-amino-2-methoxyanthracene-9,10-dione(10165-33-0)

Safety Data

• Hazardous Substances Data: 10165-33-0(Hazardous Substances Data)

Usage

Chemical Family

Anthraquinone

Central Structure

Anthracene ring

Attached Groups

Amino group and methoxy group

Potential Applications

Organic electronics, dye precursor, reagent in organic synthesis

Properties

Fluorescent and semiconductor properties

Research and Industrial Applications

Valuable for various research and industrial applications due to its unique structure and properties.

Upstream product

• 56600-57-8 2-methoxy-1-nitro-anthraquinone 
• 568-98-9 1-amino-2-hydroxy-9,10-anthracenedione 
• 77-78-1 dimethyl sulfate 
• 3274-20-2 2-methoxy-9,10-anthraquinone 
• 2872-48-2 1,4-diamino-2-methoxy-9,10-anthraquinone 
• 7732-18-5 water 
• 605-32-3 2-hydroxy-9,10-anthraquinone 

Relevant articles and documents

Transformation of dyes and related compounds in anoxic sediment: kinetics and products

The reactions of several azo, anthraquinone, and quinoline dyes were studied in settled sediments. Both the anthrone from Disperse Red 9 and the demethylation product of Disperse Red 11 reacted with half-lives of a few months, but other major products were not detected. An azo dye (Solvent Red 1) and a quinoline dye (Solvent Yellow 33) were transformed with half-lives of a few days andmonths, respectively. -from Authors

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.