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9-Ethylfluorene

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Identification
Molecular formula
C15H14
CAS number
342-35-0
IUPAC name
9-ethyl-9H-fluorene
State
State

At room temperature, 9-Ethylfluorene is a solid, indicating it has a stable form under normal conditions.

Melting point (Celsius)
29.00
Melting point (Kelvin)
302.00
Boiling point (Celsius)
306.60
Boiling point (Kelvin)
579.80
General information
Molecular weight
194.28g/mol
Molar mass
194.2790g/mol
Density
1.0824g/cm3
Appearence

9-Ethylfluorene typically appears as a white to light yellow crystalline solid. Its crystalline nature gives it a shiny, reflective surface.

Comment on solubility

Solubility of 9-ethyl-9H-fluorene

9-ethyl-9H-fluorene is a compound that exhibits interesting solubility characteristics, primarily influenced by its chemical structure. Understanding its solubility is crucial for its application in chemical processes and formulations.

Solubility Characteristics

  • Solvent Compatibility: 9-ethyl-9H-fluorene tends to be soluble in non-polar solvents, such as hexane and benzene, due to its hydrocarbon structure.
  • Polarity Considerations: The compound's minimal polarity results in limited solubility in polar solvents like water.
  • Temperature Effects: Solubility may increase with temperature, following the general trend where solubility of solids in liquids increases with rising temperatures.

In summary, 9-ethyl-9H-fluorene showcases limited solubility in polar environments while displaying a greater affinity for non-polar solvents. This property should be carefully considered when utilizing the compound in different chemical contexts.

Interesting facts

Interesting Facts about 9-ethyl-9H-fluorene

9-ethyl-9H-fluorene is a fascinating compound that lies in the realm of polycyclic aromatic hydrocarbons. Here are some compelling aspects that highlight its significance in both scientific research and industrial applications:

  • Structure and Stability: This compound features a unique structure that combines an ethyl group with the fluorene backbone. This configuration enhances its stability and alters its electronic properties compared to other fluorene derivatives.
  • Optoelectronic Properties: 9-ethyl-9H-fluorene exhibits interesting optoelectronic characteristics, which can make it useful in the design and development of organic light-emitting diodes (OLEDs) and organic solar cells. The electron-donating properties of the ethyl group can lead to improved performance in these applications.
  • Potential Applications: The compound's unique properties open avenues in various fields, including:
    • As a *fluorescent dye* for biological imaging.
    • In the synthesis of advanced materials through polymerization processes.
    • As a component in the production of chemical sensors.
  • Research Significance: As a subject of study, 9-ethyl-9H-fluorene has drawn interest in the field of photophysics. Researchers explore its absorption and emission spectra, striving to understand how molecular structure influences its photophysical properties.
  • Environmental Impact: As with many compounds in its class, understanding the environmental implications of 9-ethyl-9H-fluorene is crucial. Researchers are studying its behavior in different ecological systems to assess its potential toxicity and biocompatibility.

In summary, 9-ethyl-9H-fluorene is not just an intriguing compound due to its structure but also exhibits several practical applications that could influence technology and environmental studies. As research advances, its role could evolve, revealing even more exciting possibilities in the realm of chemistry and materials science.

Synonyms
9-Ethylfluorene
9-ETHYL-9H-FLUORENE
2294-82-8
9H-Fluorene, 9-ethyl-
AN0073G1C0
Ethyl-9H-fluorene
9H-Fluorene, ethyl-
UNII-AN0073G1C0
EINECS 218-938-6
9-Ethyl-9H-fluorene #
DTXSID10872977
AKOS006282584
65319-49-5
DB-253679
NS00049174
H27798
Q27274015