42987-34-8

Basic information

• Product Name: 1-amino-2-(4-chlorophenoxy)-4-hydroxyanthraquinone
• Synonyms: 1-amino-2-(4-chlorophenoxy)-4-hydroxyanthraquinone
• CAS NO: 42987-34-8
• Molecular Formula: C₂₀H₁₂ClNO₄
• Molecular Weight: 365.76658
• EINECS: 256-041-1
• Mol File: 42987-34-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 591.7°C at 760 mmHg
• Flash Point: 311.7°C
• Appearance: /
• Density: 1.509g/cm³
• Vapor Pressure: 1.34E-14mmHg at 25°C
• Refractive Index: 1.724
• CAS DataBase Reference: 1-amino-2-(4-chlorophenoxy)-4-hydroxyanthraquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-amino-2-(4-chlorophenoxy)-4-hydroxyanthraquinone(42987-34-8)
• EPA Substance Registry System: 1-amino-2-(4-chlorophenoxy)-4-hydroxyanthraquinone(42987-34-8)

Safety Data

• Hazardous Substances Data: 42987-34-8(Hazardous Substances Data)

Usage

Chemical class

Anthraquinone derivatives

Explanation

1-amino-2-(4-chlorophenoxy)-4-hydroxyanthraquinone belongs to a group of chemical compounds that have an anthraquinone core.

Explanation

The compound has a yellowish-red color and is a solid in its pure form.

Explanation

Due to its chemical structure and properties, the compound can be used in the production of dyes and pigments, as well as in organic synthesis. The presence of the hydroxy group also makes it potentially useful in medical and pharmaceutical applications.

Explanation

The compound has an anthraquinone core, which is a heterocyclic compound known for its potent biological and pharmacological activities.

Explanation

The presence of an amino group in the structure suggests that the compound may have reactivity and affinity towards other biological molecules, which can be useful in various applications.

Explanation

The presence of a chlorophenoxy group in the structure may enhance the reactivity of the compound, making it more suitable for various applications.

Explanation

The presence of a hydroxy group in the molecule allows it to form hydrogen bonds with other molecules, which can be beneficial in medical and pharmaceutical applications.

Physical appearance

Yellowish-red solid

Potential applications

Dye and pigment manufacturing, organic synthesis, medical and pharmaceutical applications

Core structure

Anthraquinone

Amino group presence

Reactivity and affinity towards biological molecules

Chlorophenoxy group presence

Enhanced reactivity

Hydroxy group presence

Ability to form hydrogen bonds

InChI:InChI=1/C20H12ClNO4/c21-10-5-7-11(8-6-10)26-15-9-14(23)16-17(18(15)22)20(25)13-4-2-1-3-12(13)19(16)24/h1-9,23H,22H2

Downstream Products

• 76469-59-5 3-(4-Chloro-phenoxy)-5-hydroxy-anthra[1,9-cd]isoxazol-6-one 
• 76469-47-1 1-Azido-2-(4-chloro-phenoxy)-4-hydroxy-anthraquinone 
• 34376-39-1 1-(4-Chloro-phenylamino)-2,4-dihydroxy-anthraquinone 

Relevant articles and documents

Process for producing 1-amino-4-hydroxy-anthraquinones

1-Amino-4-hydroxy-2-phenoxy- or -2-alkoxyanthraquinones are obtained by reaction of a 1-amino-2-halo-4-hydroxyanthraquinone with an alcohol or phenol. The reaction is performed in an organic solvent in the presence of an alkaline-acting agent and a phase-transfer catalyst.