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Quinazoline-2,4-diamine

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Identification
Molecular formula
C8H10N2
CAS number
492-12-2
IUPAC name
3,4-dihydro-1H-isoquinoline-2-carboximidoylammonium
State
State

The compound is typically a solid at room temperature.

Melting point (Celsius)
187.00
Melting point (Kelvin)
460.00
Boiling point (Celsius)
368.00
Boiling point (Kelvin)
641.00
General information
Molecular weight
146.18g/mol
Molar mass
146.1620g/mol
Density
1.0309g/cm3
Appearence

The compound typically appears as a colorless to slightly yellow solid.

Comment on solubility

Solubility of 3,4-dihydro-1H-isoquinoline-2-carboximidoylammonium

The solubility of 3,4-dihydro-1H-isoquinoline-2-carboximidoylammonium (C8H10N2) can be quite intriguing, as the presence of both an isoquinoline structure and a carboximidoyl group plays a significant role in its solubility characteristics.

Here are some key points regarding its solubility:

  • Polar Characteristics: The amine and carboximidoyl substituents introduce considerable polarity, suggesting that this compound may exhibit better solubility in polar solvents, such as water and methanol.
  • Solvent Dependency: Depending on the pH of the solution, the solubility can vary. For instance, in an acidic environment, the ammonium group can be protonated, potentially enhancing solubility.
  • Comparison to Similar Compounds: Similar compounds often show higher solubility in alcoholic solvents compared to non-polar solvents, indicating that this compound may display similar behavior.
  • Temperature Influence: As is common with many organic compounds, an increase in temperature might improve solubility, which can be particularly useful in applications involving heating.

Overall, understanding the solubility of 3,4-dihydro-1H-isoquinoline-2-carboximidoylammonium is essential for optimizing its practical applications in various chemical processes and research scenarios.

Interesting facts

Exploring 3,4-Dihydro-1H-Isoquinoline-2-Carboximidoylammonium

3,4-Dihydro-1H-isoquinoline-2-carboximidoylammonium is a fascinating compound with a variety of intriguing properties and potential applications in different fields of chemistry and medicine. Here are some key highlights that make this compound noteworthy:

  • Structural Significance: The compound features an isoquinoline backbone, which is a pivotal structural motif in many biologically active molecules and pharmaceuticals. Isoquinolines are known for their diverse biological activities and potential therapeutic applications.
  • Potential in Medicinal Chemistry: Due to its unique structure, 3,4-dihydro-1H-isoquinoline-2-carboximidoylammonium may exhibit interesting pharmacological properties. Compounds possessing carboximidoyl functional groups can engage in hydrogen bonding, potentially enhancing their interaction with biological targets.
  • Variability in Isoforms: This compound showcases geometric variability, specifically in its dihydro form. The saturation of the cyclized structure may lead to changes in moisture sensitivity and intermolecular interactions, causing variations in its physical and chemical behavior compared to its unsaturated counterparts.
  • Synthesis Challenges: Synthesizing this compound can be complex due to the need to create the isoquinoline structure while introducing specific functional groups such as the carboximidoyl and ammonium moieties. This opens up avenues for innovation in synthesis methodologies.
  • Research Potential: As a subject of ongoing research, compounds like 3,4-dihydro-1H-isoquinoline-2-carboximidoylammonium contribute to the understanding of related chemical reactions, mechanisms, and possibly the development of novel therapeutic agents.

Overall, the study of 3,4-dihydro-1H-isoquinoline-2-carboximidoylammonium not only highlights the intricacy of organic compounds but also underscores their potential impact on future scientific discoveries and applications in medicine. With further research, we may unveil additional properties and functionalities that lie within this intriguing molecule.