1-AMINO-2-CHLORO-4-HYDROXY-9,10-ANTHRACENEDIONE

  • CasNo：2478-67-3
  • purity：99%
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Details

Factory Supply industrial standard 1-AMINO-2-CHLORO-4-HYDROXY-9,10-ANTHRACENEDIONE 2478-67-3 In Stock

  • Molecular Formula: C14H8 Cl N O3
  • Molecular Weight: 273.675
  • Vapor Pressure: 3.43E-12mmHg at 25°C 
  • Melting Point: 233-234 °C 
  • Boiling Point: 538.1°Cat760mmHg 
  • PKA: 6.41±0.20(Predicted) 
  • Flash Point: 279.2°C 
  • PSA： 80.39000 
  • Density: 1.593g/cm3 
  • LogP: 2.98440 

1-AMINO-2-CHLORO-4-HYDROXY-9,10-ANTHRACENEDIONE(Cas 2478-67-3) Usage

Chemical class

Anthracenedione derivative

Functional groups

a. Amino group (-NH2)
b. Chloro group (-Cl)
c. Hydroxy group (-OH)

Structural properties

a. Aromatic ring system
b. Quinone core
c. Substitution at positions 1, 2, and 4

Applications

a. Synthetic intermediate in pharmaceutical production
b. Organic compound synthesis

Potential uses

a. Medicinal chemistry
b. Drug development
c. Research in biological and chemical processes

General Description

1-AMINO-2-CHLORO-4-HYDROXY-9,10-ANTHRACENEDIONE is a chemical compound with the molecular formula C14H8ClNO3. It is a derivative of anthracenedione, which is a quinone compound. This specific derivative has an amino group, a chloro group, and a hydroxy group attached to the anthracenedione core. It is used as a synthetic intermediate in the production of various pharmaceuticals and organic compounds. This chemical may have application in medicinal chemistry and drug development due to its structural properties and reactivity. Additionally, it may be utilized in research related to biological and chemical processes.

InChI:InChI=1/C14H8ClNO3/c15-8-5-9(17)10-11(12(8)16)14(19)7-4-2-1-3-6(7)13(10)18/h1-5,17H,16H2

2478-67-3 Relevant articles

Process for the preparation of a mixture of 1-amino-2-chloro-4-hydroxyanthraquinone and 1-amino-2-bromo-4-hydroxyanthraquinone

-

, (2008/06/13)

A process for the preparation of a mixtu...

Process for the preparation of aromatic hydroxy compounds

-

, (2008/06/13)

The invention relates to a process for t...

2478-67-3 Process route

sulfuric acid monohydrate
50981-12-9,10193-30-3

sulfuric acid monohydrate

1-amino-2,4-dichloroanthraquinone
13432-32-1

1-amino-2,4-dichloroanthraquinone

1-amino-4-hydroxy-2-chloroanthraquinone
2478-67-3

1-amino-4-hydroxy-2-chloroanthraquinone

Conditions
Conditions Yield
With paraformaldehyde; In water;
95%
sulfuric acid monohydrate
50981-12-9,10193-30-3

sulfuric acid monohydrate

1-amino-2,4-dichloroanthraquinone
13432-32-1

1-amino-2,4-dichloroanthraquinone

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

1-amino-4-hydroxy-2-chloroanthraquinone
2478-67-3

1-amino-4-hydroxy-2-chloroanthraquinone

Conditions
Conditions Yield
In water;

2478-67-3 Upstream products

  • 13432-32-1
    13432-32-1

    1-amino-2,4-dichloroanthraquinone

  • 757129-66-1
    757129-66-1

    2-(5-amino-2,4-dichloro-benzoyl)-benzoic acid

  • 7664-93-9
    7664-93-9

    sulfuric acid

  • 82-45-1
    82-45-1

    1-amino-9,10-anthracenedione

2478-67-3 Downstream products

  • 116-85-8
    116-85-8

    4-hydroxy-1-aminoanthraquinone

  • 23753-49-3
    23753-49-3

    1-amino-4-hydroxy-2-(2'-phenylethoxy)-anthraquinone

  • 17869-07-7
    17869-07-7

    1-amino-4-hydroxy-2-(2'-hydroxyethoxy)-anthraquinone

  • 105551-31-3
    105551-31-3

    1-azido-2-(2,4,6-trimethylphenoxy)-4-hydroxyanthraquinone

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