2-Aminofluorene

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Identification

Molecular formula
C13H11N
CAS Number
153-78-6
IUPAC Name
9H-fluoren-2-amine
Molecular Weight
181.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1912g/cm3
Appearance
is due to the aromatic structure of fluorene which is modified with an amine group, adding functional versatility to the compound. The compound may appear duller or brighter in color based on the purity and environmental conditions.
Synonyms
2-aminofluorene
Interesting facts

Interesting Facts About 9H-fluoren-2-amine

9H-fluoren-2-amine, often simply referred to as fluoren-2-amine, is a captivating compound that sits at the intersection of organic chemistry and material science. Here are some compelling facts that showcase its importance:

  • Structure and Aromaticity: The structure of 9H-fluoren-2-amine features a fluorenyl group, which is a fused bicyclic aromatic compound. This unique arrangement imparts strong aromatic characteristics, making it quite stable and integral in various chemical reactions.
  • Chemical Reactivity: As an amine, it can participate in a *variety of chemical reactions*, including nucleophilic substitutions and couplings. This versatility makes it a valuable precursor in organic synthesis.
  • Applications in Material Science: Due to its distinct electronic properties, 9H-fluoren-2-amine is often utilized in the development of **organic light-emitting diodes (OLEDs)** and other optoelectronic materials, showcasing its relevance in modern technology.
  • Role in Medicinal Chemistry: This compound has garnered attention for its potential agrochemical and pharmaceutical applications. It can serve as a starting material for the synthesis of bioactive compounds with *medicinal properties*.
  • Historical Importance: The study of fluorenes dates back to the early 20th century, contributing significantly to the development of synthetic methodologies in organic chemistry.

In conclusion, 9H-fluoren-2-amine exemplifies the interplay between structure and function in organic compounds. Its applications span from electronics to pharmaceuticals, paving the way for innovations in multiple scientific fields.

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