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