Benzo[c]acridin-7-ium derivative

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Identification

Molecular formula
C23H24Cl3N3
CAS Number
123456-78-9
IUPAC Name
2-(benzo[c]acridin-7-ylammonio)ethyl-(2-chloroethyl)-ethyl-ammonium;dichloride
Molecular Weight
408.83g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3000g/cm3
Synonyms
ICR 311
Interesting facts

Exploring 2-(benzo[c]acridin-7-ylammonio)ethyl-(2-chloroethyl)-ethyl-ammonium; dichloride

This compound, with its complex structure, has fascinating characteristics and potential applications that intrigue chemists and researchers alike.

Key Features:

  • Dual Functionality: This compound contains both an ammonium group and a chloroethyl substituent, allowing it to participate in a variety of chemical reactions and interactions.
  • Biological Activity: Compounds with heterocyclic structures, such as benzo[c]acridine, are known for their interesting pharmacological properties. This compound could have potential in medicinal chemistry, targeting various biological pathways.
  • Charged Nature: The quaternary ammonium aspect of the molecule may enhance its solubility in polar solvents, increasing its bioavailability and effectiveness in potential drug formulations.
  • Research Applications: Given its complex structure, it serves as a valuable subject for studies in organic synthesis and materials science, potentially leading to innovative applications in drug development and materials engineering.

As noted by researchers in the field, "The potential of novel compounds like these lies not just in their structure but in their ability to interact with biological systems." This highlights the ongoing interest in such complex compounds, which may pave the way to new therapeutic agents or advanced materials.

In summary, 2-(benzo[c]acridin-7-ylammonio)ethyl-(2-chloroethyl)-ethyl-ammonium; dichloride exemplifies the intricate relationship between chemical structure and biological function, making it a noteworthy compound for further study.

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