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1,4-Diaminoanthracene-9,10-diol

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Identification
Molecular formula
C14H12N2O2
CAS number
99569-88-3
IUPAC name
1,4-diaminoanthracene-9,10-diol
State
State

The compound is in a solid state at room temperature. It is often encountered in laboratories as a crystalline powder. Its solid state is due to the presence of strong intermolecular forces including hydrogen bonding and π-π interactions specific to aromatic systems.

Melting point (Celsius)
270.00
Melting point (Kelvin)
543.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
240.26g/mol
Molar mass
240.2550g/mol
Density
1.3850g/cm3
Appearence

1,4-Diaminoanthracene-9,10-diol typically appears as an orange solid. The compound has a sharp, distinct coloring often associated with aromatic hydrocarbons with amino and hydroxyl groups. Due to the vivid color, it can be visually identified quite easily among other organic compounds.

Comment on solubility

Solubility of 1,4-diaminoanthracene-9,10-diol

1,4-diaminoanthracene-9,10-diol is a compound whose solubility can be quite fascinating. Its solubility characteristics depend largely on the nature of its functional groups and the overall structure of the molecule. Here are some key insights:

  • Polarity: The presence of amine (-NH2) and hydroxyl (-OH) groups suggests that this compound is likely to have increased solubility in polar solvents.
  • Solvent Interaction: It is expected to dissolve readily in water and alcohols due to hydrogen bonding capabilities.
  • Non-polar Solvents: On the other hand, its solubility in non-polar solvents (like hexane or benzene) will be limited, as these solvents cannot effectively interact with the polar regions of the molecule.
  • Concentration Dependency: The solubility may also depend on factors such as temperature and concentration, where higher temperatures could enhance dissolution rates.

In summary, while 1,4-diaminoanthracene-9,10-diol shows a promising solubility profile in polar solvents due to its functional groups, it demonstrates limited solubility in non-polar environments. This compound beautifully illustrates how functional group chemistry can significantly influence solubility characteristics!

Interesting facts

Interesting Facts about 1,4-Diaminoanthracene-9,10-diol

1,4-Diaminoanthracene-9,10-diol is a fascinating organic compound that draws attention both for its unique structure and its potential applications. Here are some intriguing aspects of this compound:

  • Structure and Composition: This compound features an anthracene backbone, which consists of three fused benzene rings. The presence of amino groups at the 1 and 4 positions contributes to its reactivity and interaction with other molecules.
  • Colorism and Dyes: Due to its conjugated system, 1,4-diaminoanthracene-9,10-diol is capable of exhibiting vibrant colors in solutions. This property makes it an interesting candidate in the field of dyes and pigments.
  • Potential in Electronics: The electronic properties of this compound suggest possible applications in organic semiconductor materials. Researchers are exploring its use in organic light-emitting diodes (OLEDs) and organic photovoltaic cells, which could revolutionize energy-efficient technologies.
  • Biological Activities: Some studies have indicated that derivatives of 1,4-diaminoanthracene-9,10-diol possess antitumor properties. This opens the door for potential pharmaceutical applications, although further research is needed to fully understand its biological effects.
  • Synthesis Challenges: The synthesis of this compound can be complex and may involve multi-step reactions. This complexity provides a rich area for research in synthetic organic chemistry, highlighting the ingenuity of chemists in producing valuable compounds.

In summary, 1,4-diaminoanthracene-9,10-diol is more than just a compound with a complex name. It embodies the intersection of chemistry, technology, and biology, making it a subject of ongoing research and significant interest in various scientific fields. As one researcher put it, *"The study of such compounds can lead to breakthroughs in both material sciences and medicinal chemistry."*
Embracing its properties could unlock new possibilities in functional materials and therapeutic developments.

Synonyms
5327-72-0
9,10-Anthracenediol, 1,4-diamino-
1,4-Diamino-9,10-anthracenediol
Leuko-1,4-diaminoanthrachinon
NSC 3393
EINECS 226-210-4
Leuko-1,4-diaminoanthrachinon [Czech]
BRN 2813073
1,4-Diamino-9,10-dihydroxyanthraquinone
AI3-22043
Anthraquinone, 1,4-diamino-9,10-dihydroxy-
1,4-Diamino-9,10-dihydroxyanthracen [Czech]
1,4-Diamino-9,10-dihydroxyanthracen
1,4-Diamino-9,10-dihydroxyanthrachinon [Czech]
1,4-Diamino-9,10-dihydroxyanthrachinon
DTXSID6063779
4-13-00-02883 (Beilstein Handbook Reference)
DTXCID2041385
1,4-Diaminoanthracene-9,10-diol
Leuco-1,4-diaminoanthraquinone
1,10-dihydroxyanthracen
Anthracene-9, 1,4-diamino-
SCHEMBL13219065
BDBM50637
cid_5354979
NSC3393
NSC-3393
AKOS027378686
AS-60437
NS00032701
A12606
1,4-diamino-2,3-dihydroanthracene-9,10-quinone
1,4-bis(azanyl)-2,3-dihydroanthracene-9,10-dione