7-Amino-9H-fluoren-2-ol

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Identification

Molecular formula
C13H11NO
CAS Number
4791-25-5
IUPAC Name
7-amino-9H-fluoren-2-ol
Molecular Weight
195.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.0000g/cm3
Synonyms
7-Amino-9H-fluoren-2-ol
Interesting facts

Interesting Facts about 7-amino-9H-fluoren-2-ol

This intriguing compound, 7-amino-9H-fluoren-2-ol, is notable for its unique structure and useful applications in various fields. As a derivative of fluorene, it features an amino group and a hydroxyl group that contribute to its distinctive properties. Here are some fascinating aspects:

  • Biomedical Significance: Due to its amino and hydroxyl functional groups, 7-amino-9H-fluoren-2-ol has potential applications in medicinal chemistry. It could act as a precursor for pharmaceuticals or biological probes.
  • Synthesis Versatility: The compound can be synthesized through various methods, showcasing the creativity of synthetic organic chemistry. Common pathways involve functionalization of the fluorene structure while retaining its aromatic character.
  • Fluorescent Properties: The fluorene backbone is known for its fluorescence, which makes 7-amino-9H-fluoren-2-ol interesting for applications in fluorescence microscopy and as a fluorescent marker in biological studies.
  • Research Applications: Researchers are investigating its potential to be used in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its electronic properties.
  • Historical Context: The study of fluorene derivatives has a rich history in organic chemistry. The compound highlights the evolution of studies focusing on polycyclic aromatic compounds, which have paved the way for many discoveries in the field.

As a chemist or student, delving into the study of 7-amino-9H-fluoren-2-ol offers a remarkable opportunity to explore the intersection of fundamental chemistry and practical applications. Its versatility and potential make it a fascinating compound worthy of further research.

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