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9-Phenylacridine

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Identification
Molecular formula
C19H14N2
CAS number
3379-90-0
IUPAC name
N-phenylacridin-9-amine
State
State

At room temperature, N-Phenylacridin-9-amine is in a solid state. It is generally stable at ambient conditions.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.15
Boiling point (Celsius)
485.00
Boiling point (Kelvin)
758.15
General information
Molecular weight
257.33g/mol
Molar mass
257.3080g/mol
Density
1.2158g/cm3
Appearence

N-Phenylacridin-9-amine appears as a crystalline solid. It typically has a yellow to pale-yellow coloration when pure. The compound may form needles or platelets upon crystallization, and its exact hue can vary slightly based on purity and crystallization conditions.

Comment on solubility

Solubility of N-phenylacridin-9-amine

N-phenylacridin-9-amine, a compound with the chemical formula C15H12N2, exhibits intriguing solubility properties. Understanding its solubility behavior is essential for its applications in various fields like organic synthesis and materials science.

General Solubility Behavior

The solubility of N-phenylacridin-9-amine can be categorized based on several factors:

  • Polarity: This compound is largely non-polar due to its extensive aromatic structure, leading to low solubility in polar solvents like water.
  • Solvent Compatibility: N-phenylacridin-9-amine demonstrates better solubility in non-polar organic solvents such as chloroform, toluene, and ethanol.
  • Temperature Influence: Solubility generally increases with temperature, making warm solvents more effective for dissolving this compound.

Applications and Implications

The limited water solubility of N-phenylacridin-9-amine means that:

  • When used in biological environments, careful consideration must be given to the choice of solvent to ensure effective interaction.
  • In industrial applications, it is crucial to select appropriate organic solvents to achieve desired concentrations.

In summary, the solubility of N-phenylacridin-9-amine is predominantly influenced by its non-polar characteristics and the nature of the solvent used. Understanding these factors enables chemists and researchers to optimize its use in various applications.

Interesting facts

Interesting Facts about N-phenylacridin-9-amine

N-phenylacridin-9-amine is a fascinating organic compound with significant implications in the field of chemistry and materials science. Here are some intriguing highlights:

  • Diverse Applications: This compound is studied for its potential use in organic electronics, particularly in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics. Its unique molecular structure enhances its ability to exhibit desirable electronic properties.
  • Fluorescent Properties: N-phenylacridin-9-amine displays fluorescence, making it valuable for applications in biological imaging and dye-sensitized solar cells. Its fluorescent features are essential for tracking and diagnosing biological processes in research.
  • Structural Characteristics: The acridine core in its structure contributes to its stability and electron-accepting capabilities. The phenyl group further modifies its electronic attributes, enabling specific interactions with various substrates.
  • Research Implications: Scientists are exploring the potential of N-phenylacridin-9-amine in drug discovery and development, particularly in targeting cancerous cells. Studies suggest it can interact with DNA, providing insights into its mechanisms of action.
  • Interdisciplinary Interest: This compound bridges the disciplines of organic chemistry, materials science, and biochemistry, making it a subject of interest for researchers across various fields.

Overall, N-phenylacridin-9-amine is not just an ordinary organic compound; its versatility and robust electronic properties make it a subject of exciting ongoing research.

Synonyms
9-Anilinoacridine
N-Phenyl-9-acridinamine
9-Acridinamine, N-phenyl-
ACRIDINE, 9-ANILINO-
9-(Phenylamino)acridine
Acridin-9-yl-phenyl-amine
BRN 0210868
DTXSID20187044
5-22-11-00011 (Beilstein Handbook Reference)
DTXCID30109535
9-Acridinamine, N-phenyl-(9CI)
lnvqbbhypgfsmx-uhfffaoysa-n
N-phenylacridin-9-amine
3340-22-5
CHEMBL49436
SCHEMBL902770
N-(9-Acridinyl)-N-phenylamine #
BDBM50623672
AKOS002710482