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6-Ethyltetrahydro-9,10-anthraquinone

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Identification
Molecular formula
C16H16O2
CAS number
54887-12-6
IUPAC name
6-ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione
State
State

At room temperature, the compound is a solid. It is not particularly volatile, and remains stable as a solid under normal laboratory conditions.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.20
Boiling point (Celsius)
315.50
Boiling point (Kelvin)
588.70
General information
Molecular weight
236.28g/mol
Molar mass
236.2760g/mol
Density
1.2345g/cm3
Appearence

The compound generally appears as a yellow crystalline solid. It can exhibit a range of shades, primarily depending on purity and particle size.

Comment on solubility

Solubility of 6-ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione

When considering the solubility of 6-ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione, it is essential to explore several key aspects that impact its behavior in various solvents:

  • Polarity: The presence of the ethyl group and the dione functionality affects the polarity of the molecule. Generally, compounds with polar functional groups tend to be more soluble in polar solvents.
  • Solvent Effects: The choice of solvent is critical. This compound is likely to be soluble in organic solvents like ethanol, acetone, and dichloromethane, but may have limited solubility in water due to its organic nature.
  • Temperature Influence: Solubility can also vary with temperature. As the temperature increases, solubility in most solvents typically increases, offering better dissolving conditions.
  • Concentration Factor: The concentration of the solution can affect perceived solubility; supersaturation can sometimes occur under specific conditions.

In summary, while 6-ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione might not present extensive solubility data, its solubility characteristics are closely related to the type of solvent used and environmental factors. It is advisable to conduct experimental assessments to fully characterize its solubility profile, as each scenario may yield different results.

Interesting facts

Interesting Facts About 6-Ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione

6-Ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione is a fascinating compound that captures the interest of chemists and researchers alike. Here are some noteworthy aspects of this intriguing molecule:

  • Structure and Composition: This compound belongs to the class of anthraquinones, which are well-known for their unique tetracyclic structure, featuring fused aromatic rings. The presence of an ethyl group adds a hydrophobic characteristic that may influence its chemical interactions.
  • Reactivity: The 9,10-dione functional group is particularly significant, as it can undergo various reactions, making it a versatile precursor in organic synthesis. Its reactivity can lead to the formation of more complex molecules, opening doors to innovations in materials science.
  • Applications: Compounds similar to 6-ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione are often explored in the context of dyes, pigments, and even pharmaceuticals. Their ability to engage in light absorption and energy transfer makes them candidates for applications in solar cells and photodynamic therapy.
  • Research Potential: Studies have suggested that compounds of this nature could possess unique electronic properties, making them valuable in the field of organic electronics. Researchers are actively examining their potential for use in organic light-emitting diodes (OLEDs) and transistors.
  • Cultural Importance: The anthracene derivative structure is deeply rooted in the history of organic chemistry and industry, often associated with the development of synthetic dyes in the late 19th century. Discoveries surrounding these compounds have significantly shaped modern chemical practices.

In conclusion: 6-Ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione not only stands out due to its structural uniqueness but also offers a broad spectrum of potential applications and research avenues. The ongoing study of its properties can lead to groundbreaking advancements in multiple scientific domains.

Synonyms
15547-17-8
6-Ethyl-1,2,3,4-tetrahydroanthraquinone
Tetrahydro-2-ethylanthraquinone
USAF SO-2
2-Ethyl-5,6,7,8-tetrahydroanthraquinone
6-Ethyl-1,2,3,4-tetrahydroanthroquinone
BRN 2526139
EINECS 239-600-4
6Z0U5SRU0H
9,10-Anthracenedione, 6-ethyl-1,2,3,4-tetrahydro-
DTXSID8051750
Anthraquinone, 6-ethyl-1,2,3,4-tetrahydro-
2-ethyl-5,6,7,8-tetrahydro-9,10-anthraquinone
4-07-00-02483 (Beilstein Handbook Reference)
ANTHRAQUINONE, 2-ETHYL-5,6,7,8-TETRAHYDRO-
DTXCID7030305
239-600-4
6-ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione
6-ETHYL-1,2,3,4,9,10-HEXAHYDROANTHRACENE-9,10-DIONE
UNII-6Z0U5SRU0H
SCHEMBL598754
PXLXSNXYTNRKFR-UHFFFAOYSA-N
DB-318116
CS-0447245
NS00025047
I10695
Q27265746