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2,3-Dimethylfluorene

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Identification
Molecular formula
C15H14
CAS number
3421-19-6
IUPAC name
2,3-dimethyl-9H-fluorene
State
State

At room temperature, 2,3-Dimethylfluorene is in a solid state. It is stable under normal conditions and exhibits a characteristic aroma associated with aromatic hydrocarbons.

Melting point (Celsius)
72.00
Melting point (Kelvin)
345.15
Boiling point (Celsius)
323.00
Boiling point (Kelvin)
596.15
General information
Molecular weight
194.27g/mol
Molar mass
194.2640g/mol
Density
1.0150g/cm3
Appearence

2,3-Dimethylfluorene is a crystalline solid. It is typically white to off-white in color and forms needle-like or plate-like crystals. The compound is known for its luminescent properties, making it useful in organic electronic applications.

Comment on solubility

Solubility of 2,3-dimethyl-9H-fluorene

2,3-dimethyl-9H-fluorene, with a chemical formula of C13H12, exhibits notable characteristics regarding its solubility:

  • Solvent Compatibility: This compound is generally non-polar, making it more soluble in non-polar solvents such as hexane and toluene.
  • Polar Solvents: Conversely, its solubility in polar solvents like water is significantly limited, owing to the lack of polar functional groups.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature; however, specific data on solubility trends for 2,3-dimethyl-9H-fluorene at varying temperatures is sparse.

To summarize, the solubility of 2,3-dimethyl-9H-fluorene is primarily influenced by its non-polar structure, leading to affinity towards non-polar solvents. It serves as a vivid reminder of the principle: "Like dissolves like."

Interesting facts

Interesting Facts about 2,3-Dimethyl-9H-Fluorene

2,3-Dimethyl-9H-fluorene is a fascinating compound that belongs to the class of polycyclic aromatic hydrocarbons (PAHs). Here are some intriguing points to consider:

  • Structure and Stability: This compound features a unique fused ring structure that enhances its *stability* and chemical properties. The presence of methyl groups at the 2 and 3 positions of the fluorene increases the compound's *electron density*.
  • Applications: 2,3-Dimethyl-9H-fluorene is studied for its potential uses in organic electronics, including organic light-emitting diodes (OLEDs) and organic photovoltaic cells, showcasing its importance in modern technology.
  • Research Significance: This compound serves as a model for understanding the reactivity of PAHs in various chemical processes. Researchers often examine it to gain insights into *electron transfer reactions* and *photochemical behavior*.
  • Environmental Impact: As a member of the PAH family, it is essential to consider the environmental implications of its presence. Some PAHs are known for their *carcinogenic properties*, prompting studies on how to mitigate their risks in the environment.
  • Fluorene Derivatives: 2,3-Dimethyl-9H-fluorene can serve as a starting material for synthesizing other fluorene derivatives, making it significant in organic synthesis and *material chemistry*.

In summary, 2,3-dimethyl-9H-fluorene stands as a *remarkable* compound in the realm of chemistry, combining the aesthetic beauty of its structure with promising applications and significant environmental considerations. As we continue to unravel its mysteries, it remains a crucial subject for scientific inquiry!

Synonyms
2,3-Dimethylfluorene
2,3-DIMETHYL-9H-FLUORENE
CCRIS 4260
Fluorene, 2,3-dimethyl-
4612-63-9
9H-Fluorene, 2,3-dimethyl-
DTXSID20196732
DTXCID60119223
wzkbkkckpzmghv-uhfffaoysa-n
2,3-dimeth-ylfluorene
DB-239476
NS00095847