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N-Methylaziridine-1-carboxamide

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Identification
Molecular formula
C4H8N2O
CAS number
765-13-1
IUPAC name
N-methylaziridine-1-carboxamide
State
State

At room temperature, N-methylaziridine-1-carboxamide is in a liquid state. Due to its relatively low viscosity, it is readily pourable and can be handled under standard laboratory conditions.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
108.50
Boiling point (Kelvin)
381.65
General information
Molecular weight
86.12g/mol
Molar mass
86.1210g/mol
Density
0.9734g/cm3
Appearence

N-Methylaziridine-1-carboxamide appears as a colorless liquid. It is often characterized by its clear consistency and may have a slight amine odor due to its chemical nature.

Comment on solubility

Solubility of N-methylaziridine-1-carboxamide

N-methylaziridine-1-carboxamide, with the chemical formula C4H8N2O, displays intriguing solubility characteristics that are essential for its applications in various chemical environments. Understanding its solubility can provide insights into its behavior in solutions, which is crucial for both theoretical and practical applications.

Aqueous Solubility

This compound is known to be relatively soluble in water, attributed to the presence of the carboxamide group. The factors affecting its solubility include:

  • Polarity: The amide functional group introduces polarity, enhancing its interaction with water molecules.
  • Hydrogen Bonding: N-methylaziridine-1-carboxamide can form hydrogen bonds with water, significantly increasing its solubility.
  • Molecular Size: Its relatively small molecular size facilitates easier dispersal in an aqueous environment.

Solvent Versatility

Besides water, N-methylaziridine-1-carboxamide is also expected to be soluble in a variety of organic solvents, including:

  • Alcohols: Due to their polar nature, alcohols can effectively dissolve this compound.
  • Amines: Similar to alcohols, amines can interact favorably with the amide functional group.
  • Aromatics: Certain aromatic solvents can also dissolve this compound, though to a lesser extent.

Practical Implications

Understanding the solubility of N-methylaziridine-1-carboxamide is vital for its applications in various fields, such as:

  • Synthesis: Its solubility can affect reaction rates and product yields.
  • Formulations: Knowledge of solubility is crucial in developing effective pharmaceuticals and agrochemicals.

In conclusion, the solubility of N-methylaziridine-1-carboxamide is a key property that influences its utility across many disciplines, making it an exciting compound to study.

Interesting facts

Interesting Facts about N-methylaziridine-1-carboxamide

N-methylaziridine-1-carboxamide is a fascinating compound with a range of intriguing characteristics that make it a subject of interest in the fields of organic chemistry and pharmacology. Here are some key points to consider:

  • Unique Structure: This compound features a three-membered aziridine ring, which contributes to its unique reactivity and functional properties. The nitrogen atom in the ring adds to its chemical versatility.
  • Biological Significance: Compounds similar to N-methylaziridine-1-carboxamide have been studied for their potential applications in medicinal chemistry, notably in the development of antiviral and antitumor agents.
  • Reactivity: As an aziridine derivative, this compound exhibits interesting reactivity profiles including ring-opening reactions, which can lead to the formation of various synthetic intermediates. This property makes it valuable in synthetic organic chemistry.
  • Research Potential: The incorporation of the carboxamide group enhances its ability to form hydrogen bonds, potentially influencing its solubility and interaction with biological macromolecules. This makes it an interesting candidate for further research.
  • Employing in Material Science: Investigations into polymers and materials that incorporate aziridine derivatives suggest the potential for innovative material applications, which could lead to advancements in polymer science.

In summary, N-methylaziridine-1-carboxamide stands out as a compound of significant interest due to its unique structural configurations and potential applications in various experimental fields. As scientists continue to explore its properties, we may unlock new and exciting uses for this versatile compound.

Synonyms
N-Methylethyleneurea
N-Methyl-1-aziridinecarboxamide
1-AZIRIDINECARBOXAMIDE, N-METHYL-
N,N-Ethylene-N'-methylurea
13279-24-8
BRN 0108541
DTXSID00157801
4-20-00-00017 (Beilstein Handbook Reference)
DTXCID0080292
N-methylaziridine-1-carboxamide
N-methylcarbamoylaziridine
AKOS006355885