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Ametantrone

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Identification
Molecular formula
C9H16N6O
CAS number
7681-28-1
IUPAC name
2-(ethylamino)-6-(isopropylamino)-1H-1,3,5-triazin-4-one
State
State
This compound is usually a solid at room temperature.
Melting point (Celsius)
174.50
Melting point (Kelvin)
447.65
Boiling point (Celsius)
287.50
Boiling point (Kelvin)
560.65
General information
Molecular weight
225.27g/mol
Molar mass
225.2740g/mol
Density
0.9195g/cm3
Appearence

The compound typically appears as a colorless to pale yellow crystalline solid.

Comment on solubility

Solubility of 2-(ethylamino)-6-(isopropylamino)-1H-1,3,5-triazin-4-one

The solubility of 2-(ethylamino)-6-(isopropylamino)-1H-1,3,5-triazin-4-one can be described as follows:

  • Polar vs. Non-Polar: Due to the presence of both ethylamino and isopropylamino functional groups, this compound exhibits a mix of polar and non-polar characteristics, which can influence its solubility in various solvents.
  • Water Solubility: Generally, compounds containing amino groups tend to be more soluble in water; however, the overall hydrophobic nature imparted by the isopropyl group can reduce this solubility to some extent.
  • Organic Solvents: This compound may show increased solubility in organic solvents such as ethanol or methanol, which can better accommodate the hydrophobic isopropyl moiety.
  • Temperature Effects: As with many organic compounds, solubility can vary significantly with temperature. Increased temperatures typically enhance solubility due to greater molecular motion.

In summary, while 2-(ethylamino)-6-(isopropylamino)-1H-1,3,5-triazin-4-one displays potential for solubility in polar solvents due to its amino groups, the hydrophobic influences from its isopropyl group must be considered. Thus, the solubility can be characterized as moderate and depends on the solvent choice and environmental conditions.

Interesting facts

Interesting Facts about 2-(ethylamino)-6-(isopropylamino)-1H-1,3,5-triazin-4-one

This compound is a fascinating member of the triazine family, known for its versatility in various chemical applications. Triazines, particularly those with amino substitutions, exhibit a wide range of biological and chemical activities, making them a significant topic of study in both organic chemistry and pharmacology.

Key Properties and Applications:

  • Amino Functionality: The presence of both ethylamino and isopropylamino functional groups introduces striking reactivity and potential for hydrogen bonding, which may influence the compound's biological efficacy.
  • Research Significance: Compounds with triazine structures have been recognized for their applications in agrochemicals, particularly as herbicides and fungicides, due to their ability to interact with specific biological pathways.
  • Biological Activity: There has been increasing interest in the pharmacological properties of triazines, with some derivatives showing antibacterial, antifungal, and even anticancer activities.
  • Stability and Reactivity: The stability of triazines under various conditions makes them suitable for various applications, particularly in environments that challenge other compounds.

Moreover, the synthesis of this compound typically involves multistep reactions, which can be both challenging and insightful. Chemists often highlight the operational methodologies and utilization of reagents in the preparation, showcasing how small changes in the chemical structure can dramatically affect the compound's properties and potential applications.

As stated by a prominent chemist in the field, "Understanding the subtleties of structure-activity relationships in triazines can open the door to groundbreaking discoveries in pharmacology and agriculture." Thus, 2-(ethylamino)-6-(isopropylamino)-1H-1,3,5-triazin-4-one is not merely an academic curiosity; it represents the intersection of chemistry and practical application, paving the way for future innovations.