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2-Methoxyfluorene

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Identification
Molecular formula
C14H12O
CAS number
123-06-8
IUPAC name
2-methoxy-9H-fluorene
State
State

The compound is a solid at room temperature.

Melting point (Celsius)
56.00
Melting point (Kelvin)
329.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
196.24g/mol
Molar mass
196.2370g/mol
Density
1.1190g/cm3
Appearence

2-Methoxyfluorene appears as a white to pale yellow crystalline powder. It exhibits bright fluorescence, which is a common characteristic of fluorene derivatives. The compound is generally stable under normal conditions but should be stored in a dry, cool place to maintain its integrity.

Comment on solubility

Solubility of 2-methoxy-9H-fluorene

2-methoxy-9H-fluorene, with the chemical formula C14H12O, exhibits interesting solubility characteristics that are worth exploring. Being an aromatic compound containing both a methoxy group and a fluorene backbone, it tends to possess limited solubility in water, which is typical for many organic compounds.

Key points regarding its solubility include:

  • Solvent Preference: 2-methoxy-9H-fluorene is generally more soluble in organic solvents such as ethanol, chloroform, and ether.
  • Temperature Effect: Typically, an increase in temperature can enhance its solubility in organic solvents.
  • Hydrophilicity vs. Hydrophobicity: The presence of the methoxy group provides some polar character, yet the overall structure leans towards being hydrophobic, influencing its limited interaction with water.

In practical applications, understanding the solubility of 2-methoxy-9H-fluorene is crucial for its incorporation in various chemical processes and formulations. As with many compounds, it highlights the balance between hydrophilic and hydrophobic characteristics, impacting its behavior in different environments.

Interesting facts

Exploring 2-Methoxy-9H-Fluorene

2-Methoxy-9H-fluorene is a fascinating organic compound belonging to the class of fluorene derivatives. Its unique structure and functional group provide a rich platform for scientific exploration.

Unique Characteristics

  • Substituted Fluorene: The methoxy group (-OCH3) attached to the fluorene backbone introduces distinct chemical properties, making it reactive under specific conditions.
  • Potential Applications: This compound has garnered interest in organic synthesis and materials science due to its potential use in creating organic electronics, such as OLEDs (Organic Light Emitting Diodes).
  • Fluorescence: Compounds like 2-methoxy-9H-fluorene exhibit fluorescence properties, which can be harnessed in various analytical techniques and applications, including sensing and imaging technologies.

Significance in Research

Studying 2-methoxy-9H-fluorene allows chemists to delve deeper into the interactions of functional groups in organic compounds. The methoxy group enhances solubility in organic solvents, which can facilitate reactions and purifications:

  • The role of methoxy: This functional group is known to donate electron density to the aromatic system, influencing the compound's reactivity.
  • Reactivity: The molecule can participate in various chemical reactions, including electrophilic substitutions, making it a valuable subject for synthetic organic chemistry.

In summary, 2-methoxy-9H-fluorene is not just another organic compound; it represents a blend of functionalized aromatic chemistry with practical applications in modern technology. As researchers continue to unveil the complexities of such compounds, the possibilities for innovation remain limitless.

Synonyms
2-METHOXY-9H-FLUORENE
Fluorene, 2-methoxy-
2-Methoxyfluorene
2523-46-8
9H-Fluorene, 2-methoxy-
Fluoren-2-yl methyl ether
NSC60818
fluoren-2-yl-methyl ether
2-Methoxy-9H-fluorene #
SCHEMBL2914928
DTXSID90179890
NSC 60818
NSC-60818