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Glycylurea

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Identification
Molecular formula
C4H9N3O2
CAS number
591-03-1
IUPAC name
2-amino-N-carbamoyl-acetamide
State
State

At room temperature, glycylurea is a solid. Its stability in solid form makes it suitable for various chemical applications and storage.

Melting point (Celsius)
151.00
Melting point (Kelvin)
424.15
Boiling point (Celsius)
263.15
Boiling point (Kelvin)
536.30
General information
Molecular weight
117.14g/mol
Molar mass
117.1050g/mol
Density
1.4602g/cm3
Appearence

Glycylurea typically appears as a white to off-white, crystalline powder. It is odourless and has a somewhat bitter taste. The crystals are usually well-formed and may exhibit various forms depending on the crystallization conditions.

Comment on solubility

Solubility of 2-amino-N-carbamoyl-acetamide (C4H9N3O2)

2-amino-N-carbamoyl-acetamide, commonly referred to as a derivative of acetamide, presents noteworthy solubility characteristics that can greatly influence its applications in various chemical processes. Generally, this compound is expected to exhibit:

  • High solubility in water: The presence of both amine and carbamoyl functional groups increases its ability to interact with water molecules, thus promoting dissolution.
  • Influence of pH: Changes in the pH of the solution can affect its ionization, which may further impact solubility. For instance, increased acidity can lead to protonation, enhancing solubility.
  • Temperature effects: As with many compounds, an increase in temperature typically results in increased solubility, allowing for better dissolution in solvent systems.

In summary, 2-amino-N-carbamoyl-acetamide is a compound displaying favorable solubility traits, attributed to its functional groups which enhance its interaction with aqueous environments. This solubility is essential for its use in pharmaceutical contexts and chemical reactions.

Interesting facts

Interesting Facts about 2-Amino-N-carbamoyl-acetamide

2-Amino-N-carbamoyl-acetamide, also known by its IUPAC name, is a fascinating compound within the realm of organic chemistry. Here are some compelling insights regarding its structure, properties, and applications:

  • Unique Structure: This compound features a combination of amino and carbonamide functional groups, which plays a crucial role in its reactivity and interactions with other molecules.
  • Biological Relevance: Compounds like 2-amino-N-carbamoyl-acetamide are often studied for their potential roles in biological systems, particularly in the context of metabolic pathways and enzyme regulation.
  • Synthesis Potential: The synthesis of this compound can be vital for the development of pharmaceuticals and agrochemicals, showcasing its importance in industrial applications.
  • Research Interest: With ongoing research, compounds such as this one are gaining attention for their potential therapeutic effects, especially in the field of medicine. As noted in various studies, “Exploring small molecules like 2-amino-N-carbamoyl-acetamide can lead to breakthroughs in drug discovery.”
  • Versatility: The presence of both amino and carbamoyl functional groups provides this compound with a variety of possible interactions, enabling it to be a versatile building block for more complex chemical structures.

In conclusion, 2-amino-N-carbamoyl-acetamide stands out not merely as a simple chemical entity but as a compound with possible implications in health sciences and material synthesis. Its study might pave the way for advancements in various fields, making it a compound worth exploring further.

Synonyms
2-amino-N-carbamoylacetamide
N-carbamylglycinamide
SCHEMBL163295
AKOS000247801
137023-85-9