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Glallycine

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Identification
Molecular formula
C14H22N2O4
CAS number
476-97-3
IUPAC name
5-allyl-5-(1-propoxyethyl)hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, Glallycine is a solid.

Melting point (Celsius)
181.00
Melting point (Kelvin)
454.15
Boiling point (Celsius)
334.00
Boiling point (Kelvin)
607.15
General information
Molecular weight
310.36g/mol
Molar mass
310.3590g/mol
Density
1.0810g/cm3
Appearence

Glallycine is typically a white crystalline solid. It may present as a powder or in crystalline form depending on how it is processed or purified.

Comment on solubility

Solubility of 5-allyl-5-(1-propoxyethyl)hexahydropyrimidine-2,4,6-trione

The solubility of 5-allyl-5-(1-propoxyethyl)hexahydropyrimidine-2,4,6-trione is an intriguing aspect to consider, especially given its complex structure. This compound features both aliphatic and aromatic elements, which can influence its interactions with solvents. Here are several key points regarding its solubility:

  • Polar vs. Nonpolar Solvents: The presence of the propoxy group may grant some level of polarity to the compound, making it more soluble in polar solvents like water or alcohols.
  • Temperature Dependence: Solubility can vary significantly with temperature. As a general rule, solubility tends to increase with temperature, which could play a role in practical applications.
  • Hydrogen Bonding: The hydroxyl group, if present, contributes to hydrogen bonding, potentially enhancing solubility in water.
  • Group Interactions: The allyl group may introduce steric hindrance, potentially affecting solubility in various solvents.

It is often observed that "like dissolves like," meaning that compounds with similar polarity and functional groups are likely to be more soluble in each other. Thus, understanding the balance of polar and nonpolar characteristics is essential for anticipating solubility outcomes. The detailed study of solubility behavior for this compound could provide insights into its utilization in different chemical processes and applications.

Interesting facts

Exploring 5-allyl-5-(1-propoxyethyl)hexahydropyrimidine-2,4,6-trione

5-allyl-5-(1-propoxyethyl)hexahydropyrimidine-2,4,6-trione is a fascinating compound that showcases the intricate world of organic chemistry. This unique structure belongs to the broader class of pyrimidines, which are characterized by their six-membered heterocyclic rings that contain nitrogen atoms.

Key Features

  • Multifunctional Properties: This compound is a derivative of hexahydropyrimidine, providing it with a diverse reactivity that can lead to various chemical transformations.
  • Biological Significance: Compounds similar to 5-allyl-5-(1-propoxyethyl)hexahydropyrimidine-2,4,6-trione have been studied for their potential therapeutic applications, including use as antifungal and antibacterial agents.
  • Synthetic Interest: The synthesis of this compound can offer insights into protocol development for the creation of complex nitrogen-containing heterocycles, which are of great interest in pharmaceuticals.
  • Versatile Substituents: The presence of both the allyl and propoxyethyl groups lends this compound potential reactivity under various conditions, allowing it to partake in open-chain and cyclic reactions.

Applications and Implications

This compound's versatility opens up a myriad of possibilities for research and application in fields such as medicinal chemistry and material science. As a chemistry student or scientist, one could investigate the following:

  • Potential pathways for the synthesis of other vital compounds.
  • Reaction mechanisms that may contribute to its biological activity.
  • Implications of its structure on its reactivity and interactions with biological systems.

Overall, 5-allyl-5-(1-propoxyethyl)hexahydropyrimidine-2,4,6-trione stands as a testament to the complexity and beauty of organic molecules, encouraging further exploration into its many potential domains of influence within chemical science.

Synonyms
25651-43-8
DTXSID60948535
4,6-Dihydroxy-5-(prop-2-en-1-yl)-5-(1-propoxyethyl)pyrimidin-2(5H)-one
RefChem:1069505
DTXCID501376766
5-Allyl-5-(1-propoxyethyl)barbituric acid
BRN 0249289
BARBITURIC ACID, 5-ALLYL-5-(1-PROPOXYETHYL)-