Methyl 3-(aziridin-1-yl)prop-2-enoate

Identification

Molecular formula

C₇H₁₁NO₂

CAS number

7150-76-3

IUPAC name

methyl 3-(aziridin-1-yl)prop-2-enoate

State

This compound is in a liquid state at room temperature. It retains its liquid form due to its relatively low melting point and moderate boiling point, allowing it to be used in various chemical reactions and applications.

Melting point (Celsius)

-48.00

Melting point (Kelvin)

225.15

Boiling point (Celsius)

98.00

Boiling point (Kelvin)

371.15

General information

Molecular weight

141.16g/mol

Molar mass

141.1640g/mol

Density

1.0650g/cm³

Appearence

This compound is typically a colorless to pale yellow liquid. It may have a faint characteristic odor depending on its purity and storage conditions. The liquid is slightly viscous, allowing it to be easily manipulated for various chemical applications.

Comment on solubility

Solubility of Methyl 3-(aziridin-1-yl)prop-2-enoate

Methyl 3-(aziridin-1-yl)prop-2-enoate is a unique organic compound that exhibits variable solubility characteristics. When examining solubility, it is important to consider several factors that can affect the behavior of this compound in different solvents:

Polarity: The presence of the aziridine moiety contributes to the compound's overall polarity, which can enhance its solubility in polar solvents like water and alcohols.
Hydrophobic interactions: The prop-2-enoate part of the molecule has relatively hydrophobic properties, making it less soluble in non-polar solvents.
Temperature effects: Solubility may increase with temperature; thus, heating the solvent could lead to improved solvation of the methyl 3-(aziridin-1-yl)prop-2-enoate.
Concentration: At higher concentrations, precipitation may occur, indicating a saturation point where the solute no longer dissolves.

As a general guideline, this compound is expected to be moderately soluble in polar organic solvents and may show low solubility in non-polar solvents.
Understanding these solubility characteristics contributes to its practical applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about Methyl 3-(aziridin-1-yl)prop-2-enoate

Methyl 3-(aziridin-1-yl)prop-2-enoate is a fascinating compound with various applications in the field of organic chemistry and medicinal research.

Key Highlights

Unique Structural Features: This compound contains an aziridine ring, which is a three-membered nitrogen-containing heterocycle. Aziridines are known for their high reactivity due to ring strain, making them valuable intermediates in organic synthesis.
Versatile Reactivity: The presence of both the aziridine and the prop-2-enoate functional groups allows for diverse chemical reactivity. This enables the compound to participate in various reactions, such as cycloadditions and nucleophilic substitutions.
Potential Biological Activities: Many aziridine derivatives have been explored for their biological properties, including antimicrobial and anticancer activities. The unique structure of methyl 3-(aziridin-1-yl)prop-2-enoate could lead to novel therapeutic agents.

Research Implications

Due to its interesting properties and potential applications, methyl 3-(aziridin-1-yl)prop-2-enoate provides a rich area for research. Scientists explore:

Methods of synthesis that are efficient and eco-friendly.
Modification of its structure to enhance biological activity.
Applications in polymer chemistry, particularly in creating functional materials.

In summary, methyl 3-(aziridin-1-yl)prop-2-enoate stands out in the realm of organic compounds, showcasing how a simple modification can lead to significant advancements in chemical research and potential applications in medicine.

Synonyms

NCI60_022019