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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
State
State

The compound is typically found in a solid state at room temperature.

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
408.83g/mol
Molar mass
408.3200g/mol
Density
1.3000g/cm3
Appearence

The compound typically appears as an off-white to pale yellow powder. When dissolved, it forms a clear or slightly yellow solution.

Comment on solubility

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

The solubility of 2-(benzo[c]acridin-7-ylammonio)ethyl-(2-chloroethyl)-ethyl-ammonium;dichloride is an intriguing aspect of this compound. Understanding its solubility can help predict its behavior in various environments. Here are some key points:

  • Water Solubility: This compound is generally expected to be moderately soluble in water due to the presence of charged ammonium groups.
  • Solvent Effects: Polarity of the solvent plays a significant role, with more polar solvents likely to enhance solubility.
  • Cation-Interaction: The dichloride part of the formula suggests interactions with anion species may also influence solubility.
  • Acid-Base Behavior: As a quaternary ammonium compound, its solubility may also change with pH levels, where the protonation state could affect solubility dynamics.

To summarize, "the solubility of a compound is not merely a property; it's a reflection of its interactions and affinities with solvents and impurities." Analyzing solubility can provide insights into the functional applications of this compound in fields ranging from pharmacology to materials science.

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.

Synonyms
ICR 311
NSC 133480
4310-69-4
BENZ(c)ACRIDINE, 7-(2-(2-CHLOROETHYLETHYLAMINO)ETHYLAMINO)-, DIHYDROCHLORIDE
7-(2-(Ethyl-2-chloroethyl)aminoethylamino)benz(c)acridine dihydrochloride
1,2-Ethanediamine, N'-benz(c)acridin-7-yl-N-(2-chloroethyl)-N-ethyl-, dihydrochloride
1,2-Ethanediamine, N'-benz(c)acridin-7-yl-N-(2-chloroethyl)-N-ethyl-, dihydrochloride (9CI)