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Methyl aziridine-1-carboxylate

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Identification
Molecular formula
C4H7NO2
CAS number
13433-10-8
IUPAC name
methyl aziridine-1-carboxylate
State
State

At room temperature, methyl aziridine-1-carboxylate is in a liquid state. It is known to be quite reactive due to the presence of the strained aziridine ring.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
124.00
Boiling point (Kelvin)
397.15
General information
Molecular weight
99.12g/mol
Molar mass
99.1150g/mol
Density
1.0900g/cm3
Appearence

Methyl aziridine-1-carboxylate typically appears as a clear, colorless to pale yellow liquid. It is often characterized by its pungent odor.

Comment on solubility

Solubility of Methyl Aziridine-1-Carboxylate

Methyl aziridine-1-carboxylate, with its unique structure, exhibits a distinct solubility profile that is influenced by its functional groups and the cyclic aziridine moiety. Generally, solubility can be categorized based on the solvent used:

  • Polar Solvents: Methyl aziridine-1-carboxylate is likely to be more soluble in polar solvents such as water and methanol. This is due to the presence of the carboxylate group, which can form hydrogen bonds, enhancing its ability to dissolve.
  • Non-Polar Solvents: In contrast, its solubility in non-polar solvents like hexane is expected to be quite low. The aziridine structure and carboxylate may not effectively interact with non-polar substances.

In summary, the solubility of methyl aziridine-1-carboxylate is:

  1. **Higher in polar solvents** due to hydrogen bonding capabilities.
  2. **Lower in non-polar solvents** where interactions are limited.

This solubility behaviour highlights the importance of solvent choice in applications involving this compound. As the saying goes, "like dissolves like," and understanding this principle is key to effectively utilizing methyl aziridine-1-carboxylate in various chemical environments.

Interesting facts

Interesting Facts about Methyl Aziridine-1-Carboxylate

Methyl aziridine-1-carboxylate is a fascinating compound that presents a variety of intriguing aspects for chemists and researchers. Here are some key points of interest:

  • Reactivity: The aziridine ring in methyl aziridine-1-carboxylate is known for its high reactivity, allowing it to participate in various chemical reactions. This makes it valuable in synthetic organic chemistry.
  • Versatile Building Block: It serves as a versatile building block for synthesizing other compounds, including pharmaceuticals and agrochemicals, owing to its ability to undergo ring-opening reactions.
  • Biological Significance: Compounds containing aziridine rings often exhibit biological activity. Methyl aziridine-1-carboxylate may play a role in the development of new medicinal agents, highlighting its potential as a candidate for drug discovery.
  • Applications in Polymer Science: This compound is also explored in the area of polymer science, where it can contribute to the development of new polymeric materials with unique properties.
  • Research Opportunities: The study of methyl aziridine-1-carboxylate can lead to numerous research opportunities, inviting chemists to explore its properties and reactivity mechanisms further.

In summary, methyl aziridine-1-carboxylate is more than just a simple chemical compound; it is a gateway to understanding complex chemical behaviors and applications within various scientific fields. Its unique structural characteristics and reactivity promise exciting possibilities in both theoretical and applied chemistry.

Synonyms
AZIRIDINECARBOXYLIC ACID, METHYL ESTER
671-50-1
N-Carbomethoxyaziridine
Methyl aziridinylformate
Methyl ethylenecarbamate
BRN 1341682
Carbamic acid, N,N-ethylene-, methyl ester
methoxycarbonylaziridine
SCHEMBL8603867
DTXSID50217404
METHYL 1-AZIRIDINECARBOXYLATE
AKOS024436693