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Aminoanthraquinone

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Identification
Molecular formula
C14H9NO2
CAS number
82-45-1
IUPAC name
1-aminoanthracene-9,10-dione;2-aminoanthracene-9,10-dione
State
State

Aminoanthraquinone is typically found as a solid at room temperature. It is a stable compound under normal laboratory conditions.

Melting point (Celsius)
283.00
Melting point (Kelvin)
556.00
Boiling point (Celsius)
566.00
Boiling point (Kelvin)
839.00
General information
Molecular weight
223.23g/mol
Molar mass
223.2110g/mol
Density
1.4379g/cm3
Appearence

Aminoanthraquinone typically appears as a crystalline solid with a bright yellow to orange color. This compound may be available in a powder form and has a distinct appearance characteristic of many anthraquinone derivatives.

Comment on solubility

Solubility of 1-aminoanthracene-9,10-dione and 2-aminoanthracene-9,10-dione

The solubility of organic compounds like 1-aminoanthracene-9,10-dione and 2-aminoanthracene-9,10-dione showcases interesting patterns due to their chemical structure and functional groups. These compounds may exhibit varying solubility in different solvents.

  • Polar solvents: Generally, compounds with amino groups can display increased solubility in polar solvents such as water and alcohols. However, the extent of solubility can be influenced by factors like hydrogen bonding and steric hindrance.
  • Non-polar solvents: Given their aromatic nature, these compounds may also exhibit reasonable solubility in non-polar solvents such as hexane or toluene, because of hydrophobic interactions.

It is important to note:

  1. The presence of the amino group can enhance solubility through the formation of hydrogen bonds with the solvent.
  2. Conversely, the large planar anthracene structure could limit solubility in highly polar solvents.

In conclusion, the solubility of 1-aminoanthracene-9,10-dione and 2-aminoanthracene-9,10-dione is a balance of polarity and steric effects, making them intriguing candidates for further study.

Interesting facts

Interesting Facts about 1-Aminoanthracene-9,10-dione and 2-Aminoanthracene-9,10-dione

1-Aminoanthracene-9,10-dione and 2-Aminoanthracene-9,10-dione are fascinating compounds that are part of the anthraquinone family. Both compounds possess unique chemical and physical properties, making them significant in various fields of study.

Chemical Characteristics

  • Electronic Structure: These compounds contain a conjugated system of double bonds, resulting in interesting electronic properties that can be influenced by external factors.
  • Reactivity: The amino groups (-NH2) attached to the anthracene skeleton make these compounds susceptible to various chemical reactions, including electrophilic aromatic substitution.
  • Photoactivity: They exhibit notable photochemical behavior, showing potential in organic light-emitting diodes (OLEDs) and other optoelectronic applications.

Applications

  • Fluorescent Probes: Their ability to fluoresce under UV light makes them excellent candidates for fluorescent probes in biological and environmental research.
  • Medicine: Research has indicated that these compounds may have potential as anticancer agents due to their interaction with cellular processes.
  • Dyes: They can be used as dyes in various applications, thanks to their vibrant colors and stability.

Scientific Importance

The study of 1-aminoanthracene-9,10-dione and 2-aminoanthracene-9,10-dione serves as a bridge between organic chemistry and material science. These compounds not only provide insights into the behavior of organic materials but also stimulate further research in the areas of photochemistries and nanotechnology.

As a fascinating intersection of structure and function, these compounds allow chemists to explore fundamental concepts of reactivity and electronic properties while pushing the boundaries of current technological applications.