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Amino-chloro-hydroxy-anthraquinone

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Identification
Molecular formula
C14H9ClN2O4
CAS number
81-63-0
IUPAC name
4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione
State
State

At room temperature, 4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione is typically a solid crystalline compound.

Melting point (Celsius)
302.00
Melting point (Kelvin)
575.15
Boiling point (Celsius)
655.00
Boiling point (Kelvin)
928.15
General information
Molecular weight
357.68g/mol
Molar mass
357.7400g/mol
Density
1.7350g/cm3
Appearence

The compound 4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione typically appears as a solid.

Comment on solubility

Solubility of 4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione

The solubility characteristics of 4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione are quite intriguing and can be influenced by various factors. Understanding its solubility is essential for applications in pharmaceuticals and dye industries.

  • Solvent Polarity: Generally, compounds with similar polarity will be more soluble in each other. As a polyfunctional molecule, the presence of hydroxyl groups might enhance solubility in polar solvents like water, while the aromatic system may contribute to less solubility in non-polar solvents.
  • Temperature: Increasing temperature often increases solubility for many solid compounds. Therefore, slight heating might improve the solubility of this anthraquinone derivative.
  • pH Levels: The solubility may also vary with pH; acidic or alkaline conditions can affect the ionization of amino groups, thus altering solubility properties.

As stated in various chemical literature, "the solubility of a compound is a critical aspect that can determine its reactivity and bioavailability." Therefore, further studies on 4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione's solubility in diverse environments are necessary to fully unveil its potential in various applications.

Interesting facts

4,8-Diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione: An Overview

This fascinating compound stands out due to its unique structure and versatility. Often highlighted as an important intermediate in organic synthesis, **4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione** plays a variety of roles in different scientific fields.

Key Characteristics:

  • Versatile Building Block: This compound serves as an essential **building block** for various organic materials, allowing chemists to design complex molecules.
  • Applications in Medicine: It has potential utilizations in medicinal chemistry, primarily as a **precursor** for synthesizing pharmaceutical agents.
  • Environmental Chemistry: The compound's derivatives are studied for their roles in environmental monitoring, particularly in assessing **pollutants**.
  • Dye Production: Due to its vivid colors, it is also of interest in the **dye industry**, contributing to the synthesis of dyes that are both vibrant and durable.

Chemical Insights:

One of the intriguing aspects of this compound is its multiple functional groups, which include amino, hydroxyl, and chloro groups. These functional groups impart a range of chemical properties and reactivities, making the compound a point of interest for both **theoretical and practical chemistry**. Moreover, research into its interactions has opened pathways to innovative materials and **coatings** with enhanced performance.

As a compound with a rich chemistry, **4,8-diamino-2-chloro-1,5-dihydroxy-anthracene-9,10-dione** exemplifies the intersection of fundamental research and applied sciences, proving that even complex molecules can have **far-reaching implications** in technology and medicine.

Synonyms
SCHEMBL29084157
CBVYVWGKYWSTHC-UHFFFAOYSA-N