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Amino-6-thioxo-6,9-dihydro-1H-naphtho[2,3,4-de]quinoline-7,8-dione

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Identification
Molecular formula
C14H9NO2S
CAS number
244-76-6
IUPAC name
2-amino-1-sulfanyl-anthracene-9,10-dione
State
State

At room temperature, the compound is in a solid state, specifically a crystalline solid. The vibrant color denotes its anthraquinone backbone.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
538.00
Boiling point (Kelvin)
811.15
General information
Molecular weight
283.32g/mol
Molar mass
283.3190g/mol
Density
1.5400g/cm3
Appearence

The compound appears as a solid, with a distinctive orange to red color. It is crystalline in nature, indicating a regular arrangement of molecules in its solid form. The pigmentation makes it identifiable among other anthracene derivatives.

Comment on solubility

Solubility of 2-amino-1-sulfanyl-anthracene-9,10-dione

The solubility of 2-amino-1-sulfanyl-anthracene-9,10-dione can be quite intriguing due to its unique molecular structure. Understanding its solubility is key to its potential applications in various chemical processes.

Solubility Characteristics

  • Polar Solvents: This compound tends to be more soluble in polar solvents such as water and methanol due to the presence of functional groups that can interact favorably with polar molecules.
  • Non-Polar Solvents: It exhibits limited solubility in non-polar solvents like hexane and toluene, which can be attributed to the hydrophobic nature of the anthracene ring system.
  • Temperature Influence: The solubility generally increases with temperature; therefore, warming the solvent can enhance the dissolution rate.

As 2-amino-1-sulfanyl-anthracene-9,10-dione dissolves, it can undergo various reactions that make studying its solubility essential in synthetic and analytical chemistry. The interplay of its polar and non-polar characteristics could be the key to unlocking its full potential in diverse applications.

Interesting facts

Interesting Facts about 2-amino-1-sulfanyl-anthracene-9,10-dione

2-amino-1-sulfanyl-anthracene-9,10-dione is a fascinating chemical compound with intriguing properties and applications. Here are some noteworthy aspects of this compound:

  • Structure and Stability: This compound is part of the anthraquinone family, which is known for its vibrant colors and stability under various conditions.
  • Diverse Applications: 2-amino-1-sulfanyl-anthracene-9,10-dione has been utilized in various fields, including:
    • Dyes and Pigments: Its striking color makes it a candidate for use in dyes and pigments in textiles.
    • Organic Solar Cells: The compound is explored for its role as a photosensitizer in dye-sensitized solar cells, providing an avenue for sustainable energy solutions.
    • Medicinal Chemistry: Research shows its potential in the development of pharmaceuticals, particularly due to its biological activity.
  • Functional Group: The amino and sulfanyl groups enhance reactivity, allowing for further derivatization and functionalization, which is crucial in synthetic chemistry.
  • Research Interest: Ongoing studies focus on its antioxidant properties, which may offer protective effects against oxidative stress, a factor in various diseases.

As with many specialized compounds, the importance of 2-amino-1-sulfanyl-anthracene-9,10-dione extends beyond its immediate applications, highlighting the vast possibilities of synthetic chemistry and its impact on the environment and human health. Its ability to bridge several fields of research makes it a compelling subject for study.

Synonyms
6374-73-8
1M-2AA [Russian]
ANTHRAQUINONE, 2-AMINO-1-MERCAPTO-
2-Amino-1-mercaptoanthraquinone
BRN 2810093
1M-2AA
DTXSID60213179
2-14-00-00167 (Beilstein Handbook Reference)
DTXCID10135670
2-amino-1-sulfanylanthracene-9,10-dione
2-AMINO-1-MERCAPTOANTHRACENE-9,10-DIONE
1-Merkapto-2-aminoanthrachinon