Skip to main content

9-Aminophenanthrene

ADVERTISEMENT
Identification
Molecular formula
C14H11N
CAS number
226-52-2
IUPAC name
phenanthren-9-amine
State
State

At room temperature, 9-aminophenanthrene is in a solid state.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
394.00
Boiling point (Kelvin)
667.15
General information
Molecular weight
193.25g/mol
Molar mass
193.2470g/mol
Density
1.2610g/cm3
Appearence

9-Aminophenanthrene is a crystalline solid with pale yellow color. It has a distinct aromatic smell typical of substituted aromatic amines.

Comment on solubility

Solubility of Phenanthren-9-amine

Phenanthren-9-amine, known for its distinct structure and properties, showcases a unique solubility profile. The solubility of this compound can generally be described as:

  • Solvent Dependent: It is primarily soluble in organic solvents rather than in water. This is due to its hydrophobic phenanthrene skeleton.
  • Moderate Solubility: In organic solvents such as ethanol, acetone, or chloroform, phenanthren-9-amine exhibits moderate solubility, making it suitable for various organic reactions.
  • Variability: The solubility can vary significantly with changes in temperature and solvent polarity, which can lead to fluctuations in its efficacy in different experimental setups.

One must keep in mind that while it is not soluble in water, this characteristic can be advantageous in applications where water miscibility is not desirable. The solubility of phenanthren-9-amine is a key factor in its utility in organic synthesis and as a precursor in electronic materials.

Interesting facts

Interesting Facts About Phenanthren-9-amine

Phenanthren-9-amine is a fascinating organic compound that belongs to the class of polycyclic aromatic amines. Here are some intriguing points about this compound:

  • Structure and Arrangement: Phenanthren-9-amine features a unique structure consisting of three fused benzene rings with an amine group attached at the 9-position. This intricate arrangement contributes to its chemical behavior and reactivity.
  • Biological Relevance: This compound and similar polycyclic aromatic amines have been studied for their potential biological activity, including their roles in various biochemical processes. Their structural features often lead to interesting effects in biological systems.
  • Utility in Organic Synthesis: Phenanthren-9-amine can serve as an important intermediate in the synthesis of various other chemical compounds. Its reactive amine group makes it a valuable participant in chemical reactions, particularly in the creation of dyes and pharmaceuticals.
  • Environmental Considerations: Compounds in the same category as Phenanthren-9-amine are often monitored for environmental impact due to their persistence and potential toxicity. Understanding their behavior in the environment is key for eco-toxicological studies.
  • Historical Significance: The study of polycyclic aromatic compounds like this one has a long history in organic chemistry, contributing to foundational discoveries related to aromaticity and molecular structure.

In summary, Phenanthren-9-amine is not just an ordinary organic compound; it encapsulates a synergy of structure, reactivity, and biological significance. Researchers continue to explore its applications and implications in various fields, revealing the depth and complexity of this remarkable compound.

Synonyms
9-Aminophenanthrene
Phenanthren-9-amine
Phenanthren-9-Ylamine
CCRIS 7006
UNII-7M9M5KM2XY
EINECS 213-431-6
7M9M5KM2XY
BRN 2209422
CHEBI:50475
DTXSID60241573
9Phenanthrylamine
Phenanthren9amine
DTXCID90164064
4-12-00-03443 (beilstein handbook reference)
kihqwobuuipwan-uhfffaoysa-n
947-73-9
9-PHENANTHRYLAMINE
9-Phenanthrenamine
MFCD00001177
9AP
phenanthren-9-yl-amine
9-Aminophenanthrene, 96%
BIDD:GT0223
CHEMBL83088
SCHEMBL1148967
STR02251
AKOS015854888
DB03369
PD007045
SY353453
DB-057531
NS00042844
H10540
Q27094313