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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
State
State
At room temperature, 7-Amino-9H-fluoren-2-ol is a solid. It typically forms a stable crystalline structure which is common for many fluorene derivatives.
Melting point (Celsius)
251.00
Melting point (Kelvin)
524.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
195.22g/mol
Molar mass
195.2210g/mol
Density
0.0000g/cm3
Appearence
7-Amino-9H-fluoren-2-ol typically appears as a crystalline powder. The color can vary due to purity and specific preparation methods. As a compound based on the fluorene structure, it may exhibit luminescence under UV light.
Comment on solubility

Solubility of 7-amino-9H-fluoren-2-ol

The solubility of 7-amino-9H-fluoren-2-ol can be quite intriguing due to its unique structure and functional groups. This compound features both an amino group and a hydroxyl group, contributing to its solubility properties in various solvents.


Key Points on Solubility:

  • Polar Nature: The presence of the hydroxyl group (-OH) increases the polarity of the compound, enhancing its ability to dissolve in polar solvents such as water.
  • Hydrogen Bonding: The -NH2 group can also engage in hydrogen bonding, further promoting solubility in aqueous environments.
  • Non-Polar Solvents: Conversely, the aromatic moiety of the fluorenol structure may impart some solubility in non-polar organic solvents, but this is typically limited.

In summary, while 7-amino-9H-fluoren-2-ol is expected to exhibit good solubility in water due to its polar functional groups, it may show reduced solubility in purely non-polar solvents. Understanding these solubility traits is crucial for applications involving this compound in chemical processes.

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.

Synonyms
7-Amino-9H-fluoren-2-ol
2-Hydroxy-7-aminofluorene
FLUOREN-2-OL, 7-AMINO-
9H-Fluoren-2-ol, 7-amino-
1953-38-4
7-Hydroxy-2-aminofluorene
7-Hydroxyaminofluorene
7-Aminofluoren-2-ol
CC522ZQ8VP
NSC 408373
BRN 2805051
NSC-408373
DTXSID40173186
DTXCID0095677
9H-Fluoren-2-ol, 7-amino-(9CI)
963-750-6
9H-Fluoren-2-ol,7-amino-
NSC408373
UNII-CC522ZQ8VP
fluorene, 2-amino-7-hydroxy-
AKOS006280167
DS-009375