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Trimethyl-(2-((4-oxo-3-phenylquinazolin-2(4H)-yl)thio)propyl)ammonium

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Identification
Molecular formula
C22H27N3OS
CAS number
142269-48-9
IUPAC name
trimethyl-[2-(4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl]ammonium
State
State

At room temperature, it is in a solid state, typically forming crystalline structures. The stability of the compound increases in dry and cool storage conditions.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.15
Boiling point (Celsius)
390.70
Boiling point (Kelvin)
663.85
General information
Molecular weight
359.48g/mol
Molar mass
359.4840g/mol
Density
1.3263g/cm3
Appearence

The compound is typically a white to off-white crystalline solid. It possesses a fine powdery texture and may exhibit a faint odor characteristic of organic compounds.

Comment on solubility

Solubility of Trimethyl-[2-(4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl]ammonium

When discussing the solubility of the compound Trimethyl-[2-(4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl]ammonium, several factors come into play that can influence its behavior in different solvents. Here are key points to consider:

  • Polar vs. Non-Polar Solvents: This compound is likely to exhibit different solubility characteristics depending on the nature of the solvent. Generally, compounds that contain polar functional groups tend to be more soluble in polar solvents.
  • Hydrophilic and Hydrophobic Regions: The presence of the -NH3+ group increases the hydrophilicity, while the quinazolin moiety and phenyl group contribute to a more hydrophobic character, potentially complicating its solubility profile.
  • Temperature Effects: Solubility can significantly increase with temperature. Thus, determining the solubility of this compound at varying temperatures helps in understanding its practical applications.
  • Salt Forms: If the compound is presented as a salt, its ionic nature may enhance its solubility in water compared to its free base form.
  • Interaction with Other Solutes: The solubility may also be affected by the presence of other solutes in solution, which can lead to complex formation or competition for solvation.

In conclusion, while specific solubility data for Trimethyl-[2-(4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl]ammonium may not be readily available, its solubility can be anticipated to be influenced by several important factors, which should be rigorously studied for practical applications.

Interesting facts

Exploring Trimethyl-[2-(4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl]ammonium

Trimethyl-[2-(4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl]ammonium is a fascinating compound that draws attention in the fields of medicinal chemistry and organic synthesis. Its complex structure makes it an intriguing subject for research and application. Here are some notable facts about this compound:

  • Biological Significance: This compound features a quinazoline backbone, which has been studied for its potential biological activities, including anticancer, anti-inflammatory, and antimicrobial properties.
  • Functional Group Diversity: The presence of both a sulfanyl group and a quaternary ammonium functionality provides opportunities for unique reactivity and interaction with other biomolecules.
  • Drug Development Potential: Compounds like this one can serve as lead structures in drug discovery, particularly for developing novel therapeutics targeting specific enzymes or receptors.
  • Role in Diagnostics: Due to its unique properties, modifications of similar compounds are sometimes utilized in imaging agents and diagnostic tools within biomedical applications.

In the words of chemist Dr. Alicia Harper, "The beauty of these complex compounds lies not just in their structure but in the endless possibilities they present for innovation in medicine and technology."

Given its diverse applications and the rich chemistry associated with its structure, studying trimethyl-[2-(4-oxo-3-phenyl-quinazolin-2-yl)sulfanylpropyl]ammonium can lead to exciting discoveries and advancements in drug development and materials science.