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1,2-Diaminoanthraquinone

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Identification
Molecular formula
C14H10N2O2
CAS number
82-45-1
IUPAC name
1,2-diaminoanthracene-9,10-dione
State
State

At room temperature, 1,2-Diaminoanthraquinone exists as a solid. Its form as a red crystalline powder makes it easily distinguishable from other compounds.

Melting point (Celsius)
290.00
Melting point (Kelvin)
563.00
Boiling point (Celsius)
409.00
Boiling point (Kelvin)
682.00
General information
Molecular weight
238.25g/mol
Molar mass
238.2490g/mol
Density
1.4190g/cm3
Appearence

1,2-Diaminoanthraquinone is a red crystalline powder. The compound is solid and its vivid color is a characteristic feature that makes it useful in dye applications.

Comment on solubility

Solubility of 1,2-Diaminoanthracene-9,10-dione

1,2-Diaminoanthracene-9,10-dione is a fascinating compound with specific solubility characteristics noteworthy for both research and practical applications. Its solubility can be influenced by various factors, which are crucial to understand when working with this compound:

  • Polar Solvents: Generally, the solubility of 1,2-diaminoanthracene-9,10-dione is enhanced in polar solvents like dimethyl sulfoxide (DMSO) and dimethylformamide (DMF). These solvents can interact favorably with the compound's polar amino groups.
  • Non-Polar Solvents: Conversely, this compound exhibits limited solubility in non-polar solvents such as hexane or benzene. The presence of significant polar functional groups reduces its compatibility with non-polar environments.
  • Temperature Effects: An increase in temperature may enhance solubility, as higher temperatures typically increase the kinetic energy of molecules, thus facilitating interactions in solution.

In practical terms, the solubility of this compound can be summarized as follows:

  1. Highly soluble in strong polar solvents.
  2. Poorly soluble or insoluble in non-polar solvents.
  3. Temperature-dependent solubility, requiring careful consideration during experimental procedures.

To echo the significance of solubility, it's crucial to note: "The solubility of a compound can govern its reactivity and applications in biochemical contexts." Understanding these solubility properties allows chemists to optimize conditions for various experiments and formulations involving 1,2-diaminoanthracene-9,10-dione.

Interesting facts

Interesting Facts about 1,2-Diaminoanthracene-9,10-dione

1,2-Diaminoanthracene-9,10-dione (often abbreviated as DAA) is a fascinating compound that has attracted considerable attention in the field of organic chemistry. This compound is noteworthy for several reasons:

  • Structure and Characteristics: DAA features a polycyclic aromatic structure, characterized by its fused ring system. The presence of multiple functional groups, including amino groups, enhances its chemical reactivity and versatility.
  • Applications in Science: This compound has significant applications in various fields, such as material science, organic electronics, and dye sensitized solar cells. Its electron-withdrawing dione groups make it an interesting candidate for use in organic photovoltaics.
  • Biological Interest: DAA and its derivatives have shown potential as antioxidants. They can help protect cells from oxidative stress and may play a role in pharmaceutical applications targeting diseases caused by free radicals.
  • Fluorescent Properties: The electronic properties of DAA contribute to its fluorescent characteristics. This makes it useful in fluorescent labeling and detection methods, aiding in various biological and chemical assays.
  • Synthesis Pathways: The synthesis of 1,2-diaminoanthracene-9,10-dione involves multi-step reactions that can include nitro group reductions and subsequent steps to install the amino groups, showcasing the complexity and ingenuity involved in creating such a compound.

Overall, 1,2-diaminoanthracene-9,10-dione is more than just a chemical formula; it represents a bridge between structural chemistry and pragmatic applications, illuminated by its role in advancing research and technology.

Synonyms
1,2-Diaminoanthraquinone
9,10-Anthracenedione, 1,2-diamino-
1,2-Daa
1,2-Daa [Russian]
ANTHRAQUINONE, 1,2-DIAMINO-
1,2-Diamino-9,10-anthraquinone
1,2-Diamino-9,10-anthracenedione
CCRIS 5602
UNII-H5P6YP29VA
EINECS 217-156-2
H5P6YP29VA
NSC 39934
BRN 2125604
AI3-61387
NSC-39934
DTXSID5061950
4-14-00-00456 (Beilstein Handbook Reference)
DTXCID0035586
217-156-2
lrmdxtvkvhkwek-uhfffaoysa-n
1758-68-5
1,2-diaminoanthracene-9,10-dione
1,2-diamino-10-anthracenedione
Diaminoanthraquinone
1,2-Diamino-anthraquinone
CHEMBL89626
1,2-diamino-9,10-dihydroanthracene-9,10-dione
NSC39934
MFCD00001219
9, 1,2-diamino-
Anthraquinone,2-diamino-
1, 2-Diaminoanthraquinone
BIDD:GT0412
SCHEMBL487001
BBL013159
BDBM50599586
STK396666
1,2-Diaminoanthra-9,10-quinone #
9,10-Anthracenedione,1,2-diamino-
WLN: L C666 BV IVJ DZ EZ
AKOS000120256
CS-W014151
HY-W013435
UPCMLD0ENAT5883742:001
BP-12713
DA-48996
VS-03693
9,?10-?Anthracenedione, 1,?2-?diamino-
NS00025773
EN300-18126
G66571
A03-0001
Q27279676