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3-Chloroacridin-9-amine

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Identification
Molecular formula
C13H9ClN2
CAS number
6635-84-3
IUPAC name
3-chloroacridin-9-amine
State
State

At room temperature, 3-chloroacridin-9-amine is typically a solid. It is stable under normal conditions, assuming a crystalline form.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
475.00
Boiling point (Kelvin)
748.15
General information
Molecular weight
230.68g/mol
Molar mass
230.6790g/mol
Density
1.3230g/cm3
Appearence

3-Chloroacridin-9-amine typically presents as a crystalline solid with a pale yellow to yellow-green color. The appearance may vary depending on purity and particle size. It tends to form well-defined crystal shapes.

Comment on solubility

Solubility of 3-chloroacridin-9-amine

The solubility of 3-chloroacridin-9-amine can be influenced by various factors, making its behavior in different solvents quite interesting. This compound, known for its unique structural features, generally exhibits:

  • Moderate Solubility: It shows a degree of solubility in polar solvents, but is less soluble in non-polar solvents.
  • Temperature Dependence: The solubility may increase with rising temperatures, a common trait seen in many organic compounds.
  • pH Sensitivity: Changes in pH can affect its ionization state, which in turn alters its solubility properties.

While the precise solubility data might vary, it is often important to consult specific experimental results for detailed insights. Overall, the solubility characteristics of 3-chloroacridin-9-amine not only enhance its practical applications but also contribute to its intriguing behavior in chemical reactions and processes.

Interesting facts

Interesting Facts about 3-Chloroacridin-9-amine

3-Chloroacridin-9-amine is a fascinating compound within the realm of organic chemistry, particularly known for its potential applications in pharmaceuticals and materials science. Here are some engaging insights:

  • Structural Significance: The unique structure of 3-chloroacridin-9-amine features an acridine ring system fused with a chlorine atom and an amine group. This structural arrangement contributes to its properties and functionality.
  • Biological Relevance: Compounds similar to 3-chloroacridin-9-amine have shown promise in medicinal chemistry. They are often investigated for their potential as antitumor agents and antimicrobial agents, making them of special interest in the drug development process.
  • Research Applications: This compound is commonly studied for its role in developing fluorescent probes. These probes can be utilized in biological imaging, offering a way to visualize and study cellular processes in real-time.
  • Synthetic Pathways: The synthesis of 3-chloroacridin-9-amine can involve various methodologies, allowing for the exploration of different reaction conditions and reagents. This adaptability makes it an intriguing subject for synthetic chemists.
  • Environmental Impact: Understanding and managing compounds like 3-chloroacridin-9-amine is crucial due to their environmental implications, especially concerning their stability and toxicity profiles. Studies are ongoing to evaluate how such compounds interact with biological systems and their ecological consequences.

In summary, the study of 3-chloroacridin-9-amine not only enhances our understanding of organic compounds but also opens avenues for future research in medicinal chemistry and environmental science. As scientists continue to explore its properties and applications, we can anticipate exciting developments that could influence various fields.

Synonyms
ACRIDINE, 9-AMINO-3-CHLORO-
TCMDC-141999
3407-98-5
CHEMBL146512
5-Amino-2-chloroacridine
BRN 0171910
SCHEMBL7795994
DTXSID30187671
BDBM50408800