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5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one

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Identification
Molecular formula
C12H19N3O
CAS number
.
IUPAC name
5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one
State
State
5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one is in a solid state under ambient conditions. It is relatively stable and typically found in a powdered or crystalline form.
Melting point (Celsius)
152.00
Melting point (Kelvin)
425.15
Boiling point (Celsius)
412.50
Boiling point (Kelvin)
685.65
General information
Molecular weight
222.30g/mol
Molar mass
222.3000g/mol
Density
1.1300g/cm3
Appearence

5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one typically appears as a crystalline solid. The color can range from white to an off-white, depending on the purity of the sample. It is generally a stable compound when stored in a cool, dry place, away from direct light.

Comment on solubility

Solubility of 5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one

The solubility of 5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one can be influenced by various factors, including its molecular structure and the nature of its substituents. In general, the solubility of a compound can be summarized through the following key points:

  • Polarity: The presence of polar functional groups often increases solubility in polar solvents, such as water, while non-polar components favor solubility in organic solvents.
  • Hydrogen Bonding: Compounds capable of forming hydrogen bonds with solvents tend to have higher solubility; the ethylamino group may facilitate this interaction.
  • Molecular Size: Larger molecules may exhibit lower solubility due to steric hindrance, while smaller fragments often enhance dissolution.
  • Temperature: An increase in temperature typically improves solubility, facilitating dissolution processes.

As for 5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one, while precise solubility data is essential, one might expect moderate solubility in polar solvents due to the presence of the ethylamino substituent, which could enhance interaction with water. In contrast, its butyl tail may detract from solubility in strictly aqueous environments. Thus, solubility testing in varying solvents remains crucial to understand its behavior comprehensively.

Interesting facts

Interesting Facts about 5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one

5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one is a fascinating compound in the realm of organic chemistry. As a pyrimidine derivative, it exhibits a variety of intriguing properties and applications. Here are some key points that highlight its significance:

  • Pharmacological Potential: This compound is part of a larger class of molecules that has been explored for their potential therapeutic effects. Pyrimidine derivatives are often associated with diverse biological activities, making them valuable in drug design.
  • Structure-Activity Relationship (SAR): The specific substitutions on the pyrimidine ring can greatly influence the biological activity of the compound. For instance, the presence of the butyl and ethylamino groups can modulate its interaction with biological targets.
  • Research Applications: Compounds like this one are often employed in chemical biology studies to probe nucleotide signaling pathways, shedding light on cellular processes and disease mechanisms.
  • Analytical Techniques: The study of this compound, like many others, typically involves various analytical techniques such as NMR, IR, and mass spectrometry, which help to elucidate its structure and functional groups.
  • Synthetic Challenges: The synthesis of 5-butyl-2-(ethylamino)-6-methyl-1H-pyrimidin-4-one can present challenges due to the need for specific reaction conditions and purification steps to achieve the desired purity and yield.

As students and scientists delve into the properties and reactions of pyrimidine derivatives like this one, they uncover not just a compound, but a whole landscape of chemical reactivity and biological significance. As expressed by many chemists, “The beauty of chemistry lies in the complexity and diversity of compounds that, despite their simplicity, can lead to profound discoveries.”