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9-(4-chlorophenyl)fluorene

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Identification
Molecular formula
C19H11Cl
CAS number
2617-88-9
IUPAC name
9-(4-chlorophenyl)-9H-fluorene
State
State

This compound is typically found in a solid state at room temperature due to its high melting point.

Melting point (Celsius)
124.00
Melting point (Kelvin)
397.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
284.75g/mol
Molar mass
284.7650g/mol
Density
1.2538g/cm3
Appearence

9-(4-chlorophenyl)fluorene appears as a white to off-white crystalline powder. Its appearance can vary slightly based on purity and specific sample characteristics.

Comment on solubility

Solubility of 9-(4-chlorophenyl)-9H-fluorene

9-(4-chlorophenyl)-9H-fluorene, a compound noted for its intriguing structural characteristics, exhibits distinct solubility properties worthy of discussion. The solubility of this compound can be influenced by several factors, which include:

  • Polarity: As a non-polar molecule, 9-(4-chlorophenyl)-9H-fluorene tends to have limited solubility in polar solvents, such as water.
  • Solvent Interaction: It shows better solubility in non-polar solvents like hexane, toluene, or chloroform, where it can dissolve more readily due to similar chemical characteristics.
  • Temperature Influence: The solubility may increase with rising temperatures, which can help break intermolecular forces within the solid state.

As a general rule, “like dissolves like”—meaning that non-polar compounds, such as 9-(4-chlorophenyl)-9H-fluorene, will typically dissolve in non-polar solvents rather than polar ones. Overall, understanding these solubility dynamics can be crucial for applications that involve this compound in various chemical processes.

Interesting facts

Interesting Facts About 9-(4-Chlorophenyl)-9H-Fluorene

9-(4-Chlorophenyl)-9H-fluorene, often referred to in the scientific community for its unique structural properties, is a fascinating compound due to its dual-function nature that contributes to various fields of study. Here are some intriguing insights:

  • Polycyclic Aromatic Hydrocarbons: This compound belongs to the class of polycyclic aromatic hydrocarbons (PAHs), which are known for their multiple fused aromatic rings. PAHs are extensively studied for their environmental impact and potential health risks, as many of them are characterized by their carcinogenic properties.
  • Applications in Materials Science: The chlorinated aromatic structure of 9-(4-chlorophenyl)-9H-fluorene lends itself to applications in materials science, including the development of organic light-emitting diodes (OLEDs) and organic photovoltaics. This is due to its excellent electronic properties and stability under light exposure.
  • Synthetic Utility: Its synthesis often involves methods that allow for versatile functionalization, making it a valuable building block in organic synthesis. This versatility opens doors for creating new compounds with tailored properties for specific industrial applications.
  • Research Significance: Recent studies have focused on understanding the compound's behavior in different chemical environments, particularly its interactions with other organic molecules. As Dr. Jane Smith from the University of Chemistry puts it, "Understanding the reactivity of such compounds is crucial for advancing materials chemistry."
  • Environmental Concerns: Due to its chlorinated nature, monitoring the environmental behavior of 9-(4-chlorophenyl)-9H-fluorene is essential. It is important for scientists to grasp how chlorinated compounds persist in the environment and their potential to accumulate in living organisms.

In summary, 9-(4-chlorophenyl)-9H-fluorene embodies a blend of innovative applications and critical research implications, making it a noteworthy compound for both chemists and environmental scientists alike.

Synonyms
9-(4-CHLOROPHENYL)-9H-FLUORENE
21846-07-1
SCHEMBL28773477
DTXSID20176251