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1-Methylfluorene

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Identification
Molecular formula
C14H12
CAS number
1730-37-6
IUPAC name
1-methyl-9H-fluorene
State
State
At room temperature, 1-Methylfluorene is typically solid and exists in the form of crystalline material.
Melting point (Celsius)
30.00
Melting point (Kelvin)
303.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
180.25g/mol
Molar mass
180.2450g/mol
Density
1.0827g/cm3
Appearence
1-Methylfluorene is an organic compound that typically appears as white to light yellow crystals. It is part of the polycyclic aromatic hydrocarbons (PAHs) family.
Comment on solubility

Solubility of 1-Methyl-9H-Fluorene

1-Methyl-9H-fluorene, a polycyclic aromatic hydrocarbon, exhibits interesting solubility characteristics pertinent to its molecular structure.

  • Primarily, it is considered insoluble in water due to its hydrophobic nature and considerable aromatic character.
  • However, it demonstrates good solubility in organic solvents such as:
    • Hexane
    • Toluene
    • Xylene

The relatively large nonpolar structure of 1-methyl-9H-fluorene leads to solubility behavior governed by the principle of like dissolves like. As such, it interacts favorably with nonpolar and weakly polar solvents, making it suitable for various organic synthesis applications.

In summary, when considering the solubility of 1-methyl-9H-fluorene:

  1. Insoluble in water
  2. Soluble in many organic solvents
  3. Affected by temperature and solvent polarity

Understanding these solubility traits is crucial for effective handling and utilization of this compound in laboratory settings.

Interesting facts

Interesting Facts About 1-Methyl-9H-Fluorene

1-Methyl-9H-fluorene is a fascinating compound that combines structural uniqueness with intriguing properties, making it a point of interest in various fields of chemistry. Here are some interesting facts:

  • Polycyclic Aromatic Hydrocarbon: This compound belongs to the family of polycyclic aromatic hydrocarbons (PAHs), which are known for their resonance stability and ability to engage in pi-stacking interactions.
  • Fluorene Derivative: As a derivative of fluorene, 1-methyl-9H-fluorene retains the core structure of fluorene but with an added methyl group that can influence its reactivity and properties.
  • Applications in Organic Electronics: The compound holds promise in the field of organic electronics, including applications in organic light-emitting diodes (OLEDs) and organic photovoltaic cells due to its excellent charge transport properties.
  • Synthesis Pathways: Numerous synthetic methods exist to produce this compound, including the Friedel-Crafts alkylation of fluorene, showcasing the versatility of organic synthesis techniques.
  • Research Interest: Its study has garnered attention for investigating the behavior of similar compounds in processes relevant to environmental chemistry and material sciences.

Interestingly, the presence of the methyl group at the 1-position also affects how 1-methyl-9H-fluorene interacts with other chemical species, altering its behavior in reactions and in various applications. As researchers continue to explore the unique properties of 1-methyl-9H-fluorene, it holds significant potential for future innovations within the realm of chemistry.


Synonyms
1-Methylfluorene
1-Methyl-9H-fluorene
UNII-5DR03K3111
EINECS 217-048-5
NSC 80183
NSC-80183
DTXSID4061919
Fluorene, 1methyl
9HFluorene, 1methyl
Fluorene, 1methyl (8CI)
9HFluorene, 1methyl (9CI)
DTXCID7035519
gkeuodmjrfdljy-uhfffaoysa-n
1730-37-6
Fluorene, 1-methyl-
9H-Fluorene, 1-methyl-
5DR03K3111
1-Methyl-fluorene
MFCD00001131
1-methyl-9H-fluoren
1-methyl-9H-luorene
1-Methylfluorene, 98%
1-Methyl-9H-fluorene #
NCIOpen2_000950
CHEMBL1797283
CHEBI:180972
BAA73037
NSC80183
AKOS015906715
BS-42230
CS-0236200
NS00025670
EN300-1697058
Q27261886