9-(4-chlorophenyl)fluorene

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Identification

Molecular formula
C19H11Cl
CAS Number
2617-88-9
IUPAC Name
9-(4-chlorophenyl)-9H-fluorene
Molecular Weight
284.75g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2538g/cm3
Appearance
can vary slightly based on purity and specific sample characteristics.
Synonyms
9-(4-CHLOROPHENYL)-9H-FLUORENE
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.

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