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1-Aminofluorene

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Identification
Molecular formula
C13H11N
CAS number
153-04-4
IUPAC name
9H-fluoren-1-amine
State
State

At room temperature, 1-aminofluorene is a solid. It is usually in the form of crystals or powder.

Melting point (Celsius)
128.00
Melting point (Kelvin)
401.15
Boiling point (Celsius)
332.70
Boiling point (Kelvin)
605.85
General information
Molecular weight
167.24g/mol
Molar mass
167.2210g/mol
Density
1.1500g/cm3
Appearence

1-Aminofluorene is typically a white to pale yellow solid at room temperature. The appearance can vary slightly due to impurities, but it is generally perceived as a crystalline substance.

Comment on solubility

Solubility of 9H-fluoren-1-amine

9H-fluoren-1-amine, a compound featured prominently in organic chemistry, exhibits intriguing solubility characteristics that are pivotal for its applications. Generally, the solubility of 9H-fluoren-1-amine can be summarized as follows:

  • Solvent Compatibility: 9H-fluoren-1-amine tends to be soluble in polar organic solvents such as ethanol and methanol, while its solubility in water is quite limited.
  • Temperature Influence: Like many organic compounds, the solubility of 9H-fluoren-1-amine often increases with temperature—making it more soluble in warmer solvents.
  • pH Dependency: The solubility of 9H-fluoren-1-amine can also be affected by the pH of the solution; it may become more soluble in acidic conditions due to protonation.

To summarize, while 9H-fluoren-1-amine is not significantly soluble in water, its solubility in various organic solvents allows for versatile applications in synthesis and research. Understanding these nuances not only enhances its practical usage but also supports the exploration of its potential reactions and interactions.

Interesting facts

Interesting Facts about 9H-fluoren-1-amine

9H-fluoren-1-amine, a fascinating organic compound, belongs to the family of amines and is structurally related to the polycyclic aromatic hydrocarbon fluoren. This compound exhibits a unique combination of properties and applications:

  • Structure & Stability: The compound features a rigid bicyclic structure which contributes to its stability and makes it an interesting candidate for studying molecular interactions.
  • Applications: 9H-fluoren-1-amine is often utilized in the field of organic synthesis. It serves as a pivotal intermediate in the manufacturing of various dyes, pharmaceuticals, and agrochemicals.
  • Fluorescent Properties: This compound demonstrates luminescent behavior, making it valuable in the development of fluorescent probes for biological imaging applications.
  • Research Interest: The compound is a subject of extensive research, particularly in the areas of materials science and nanotechnology due to its electronic properties and potential in creating organic semiconductors.

Interestingly, 9H-fluoren-1-amine has also been explored for its potential use in photovoltaics. Scientists are intrigued by its possibilities in improving the efficiency of solar cells. As a part of ongoing research, it may lead to the development of more sustainable energy sources.

Due to its diverse functionalities and structural characteristics, 9H-fluoren-1-amine not only enriches the field of organic chemistry but also opens new avenues in material science, making it a valuable compound worth studying.

Synonyms
1-Aminofluorene
FLUOREN-1-AMINE
CCRIS 6997
NSC 51312
UNII-4106Q2NK4E
BRN 1949036
4106Q2NK4E
NSC-51312
DTXSID90212857
4-12-00-03369 (Beilstein Handbook Reference)
DTXCID20135348
633-192-5
cyspwcardhryjx-uhfffaoysa-n
6344-63-4
9H-Fluoren-1-amine
Fluorene, 1-amino-
fluorenamine
fluorene-amine
NSC51312
1-Aminofluorene, 99%
SCHEMBL221400
AKOS015894983
DB-054481
NS00120895
Q27258367