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Mauvaniline

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Identification
Molecular formula
C22H23ClIN3OS
CAS number
137-29-5
IUPAC name
2-(7-chloro-4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl-trimethyl-ammonium;iodide
State
State

At room temperature, Mauvaniline exists as a solid.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
364.00
Boiling point (Kelvin)
637.15
General information
Molecular weight
482.85g/mol
Molar mass
482.8510g/mol
Density
1.4400g/cm3
Appearence

Mauvaniline is typically a pale yellow solid.

Comment on solubility

Solubility of 2-(7-chloro-4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl-trimethyl-ammonium iodide

The solubility of 2-(7-chloro-4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl-trimethyl-ammonium iodide can be influenced by various factors, including its ionic nature and the presence of different solvents. That being said, here are some key points to consider regarding its solubility:

  • Solvent Composition: This compound is likely to be more soluble in polar solvents due to its quaternary ammonium structure, which promotes interaction with the solvent molecules.
  • Temperature Dependence: Like many ionic compounds, its solubility may increase with temperature, making higher temperatures favorable for dissolving.
  • Iodide Ion Influence: The presence of iodide ions from the compound's salt form can enhance solubility in water compared to other halides, due to the relatively large ionic radius of iodide which can stabilize solvation.
  • pH Considerations: The solubility might also be affected by the pH of the solution; in general, cationic compounds tend to be more soluble in acidic conditions.

In conclusion, while 2-(7-chloro-4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl-trimethyl-ammonium iodide shows potential for solubility in various solvents, empirical testing is essential for determining precise solubility characteristics. Factors such as solvent polarity, temperature variations, and solution pH are key to achieving the desired solubility.

Interesting facts

Interesting Facts about 2-(7-Chloro-4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl-trimethyl-ammonium;iodide

This fascinating compound showcases the intricate interplay between medicinal chemistry and organic synthesis. As a quaternary ammonium salt, it binds to its surroundings through ionic interactions, fundamentally influencing its applications in pharmacology.

Key Insights:

  • Antimicrobial Properties: Compounds similar to quaternary ammonium salts have been noted for their effective antimicrobial activity. This property makes them potentially useful in the development of antiseptics and disinfectants.
  • Quinazoline Framework: The quinazoline moiety, known for its presence in many bioactive molecules, highlights the compound’s potential to serve as a scaffold for drug development. Quinazoline derivatives are often explored for their anticancer and antiviral activities.
  • Iodide Influence: The presence of iodide can enhance the compound's ability to engage in various chemical transformations, making it a valuable precursor in organic synthesis pathways.
  • Versatility in Applications: Beyond pharmaceuticals, this compound could find applications in materials science, particularly in the development of coatings and surfactants due to its unique structure.

As a synthesis pathway, the formation of this compound might involve several crucial steps, allowing chemists to explore diverse reaction conditions and catalysts. It serves not only as a topic of interest for medicinal chemists but also represents a platform for educational exploration in advanced organic chemistry.

In the words of chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” This compound embodies that essence: integrating multiple chemical functionalities, it provides a gateway to a realm of discoveries and innovations.

Synonyms
Ammonium, (2-((3,4-dihydro-7-chloro-4-oxo-3-phenyl-2-quinazolinyl)thio)propyl)trimethyl-, iodide
15589-18-1
DTXSID60935304
2-[(7-chloro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)sulfanyl]-N,N,N-trimethylpropan-1-aminium iodide