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9-Methylfluorene

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Identification
Molecular formula
C14H12
CAS number
2529-45-5
IUPAC name
9-methyl-9H-fluorene
State
State

At room temperature, 9-Methylfluorene exists as a crystalline solid. It is chemically stable under normal conditions but may react with strong oxidizing agents.

Melting point (Celsius)
32.50
Melting point (Kelvin)
305.65
Boiling point (Celsius)
286.00
Boiling point (Kelvin)
559.15
General information
Molecular weight
180.25g/mol
Molar mass
180.2450g/mol
Density
1.1068g/cm3
Appearence

9-Methylfluorene is an off-white to light yellow crystalline solid. It forms needle-like crystals and has a characteristic aromatic odor. The compound is not soluble in water but is soluble in organic solvents such as ethanol and ether.

Comment on solubility

Solubility of 9-methyl-9H-fluorene

9-methyl-9H-fluorene, noted for its intriguing structure, exhibits interesting solubility characteristics that relate to its aromatic nature. This compound is primarily characterized by its hydrophobic properties, which significantly affect its solubility in various solvents.

Key points regarding its solubility:

  • 9-methyl-9H-fluorene is generally insoluble in water, a common trait among non-polar organic compounds.
  • It readily dissolves in non-polar organic solvents such as hexane and benzene, showcasing its preference for similar hydrophobic environments.
  • The solubility can be enhanced in slightly polar solvents under certain conditions, but it remains primarily limited to non-polar media.

This distinct pattern of solubility highlights the importance of molecular structure in determining the behavior of compounds in various environments. As such, 9-methyl-9H-fluorene is an excellent example of how like dissolves like plays a crucial role in chemistry.

Interesting facts

Interesting Facts About 9-Methyl-9H-Fluorene

9-Methyl-9H-fluorene is a fascinating compound with unique properties and applications in the realm of organic chemistry. Here are some intriguing insights into this compound:

  • Structure & Stability: As a derivative of fluorene, 9-methyl-9H-fluorene features a methyl group at the 9-position, enhancing its structural stability. The aromatic rings contribute to the compound's stability and reactivity.
  • Applications in Materials Science: This compound is significant in materials science, especially in the development of organic semiconductors and photonic devices. Its excellent photophysical properties make it suitable for use in light-emitting diodes (LEDs) and other optoelectronic applications.
  • Research Potential: 9-Methyl-9H-fluorene has been the subject of various studies aiming to explore its electronic properties and potential in organic photovoltaics, illustrating its relevance to sustainable energy solutions.
  • Environmental Considerations: The research surrounding this compound also extends to its impact on the environment. Understanding its biodegradability and toxicity is pivotal for responsible scientific advancement.
  • Insights from Synthesis: The synthesis of 9-methyl-9H-fluorene often involves intriguing methods such as Friedel-Crafts alkylation, showcasing the complex yet fascinating pathways chemists use to create this compound.

In summary, 9-methyl-9H-fluorene embodies the interplay of chemistry and materials science, opening new avenues for research and application. As scientists and students delve deeper into its properties, the potential innovations derived from this compound continue to inspire advancements in various fields.

Synonyms
9-Methylfluorene
9-METHYL-9H-FLUORENE
Fluorene, 9-methyl-
CCRIS 4264
EINECS 219-750-7
NSC 10161
UNII-95M10BKB07
95M10BKB07
NSC-10161
DTXSID5073957
9H-FLUORENE,9-METHYL-
DTXCID4037241
zvejrzrauyjyco-uhfffaoysa-n
2523-37-7
9H-Fluorene, 9-methyl-
MFCD00126475
9-Methyl-9H-fluorene; NSC 10161
9-methyl fluorene
9-Methyl-fluorene
9-Methyl-9H-fluorene #
9-Methyl-9H-fluorene, AldrichCPR
NSC10161
AKOS003342894
s12001
AS-54555
SY239830
DB-067355
CS-0206127
NS00027836
Q27271801