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Benzyl 3-(aziridin-1-yl)propanoate

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Identification
Molecular formula
C13H15NO2
CAS number
105379-91-1
IUPAC name
benzyl 3-(aziridin-1-yl)propanoate
State
State

At room temperature, Benzyl 3-(aziridin-1-yl)propanoate is a liquid.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
205.27g/mol
Molar mass
205.2670g/mol
Density
1.0673g/cm3
Appearence

Benzyl 3-(aziridin-1-yl)propanoate typically appears as a colorless to slightly yellow liquid.

Comment on solubility

Solubility of Benzyl 3-(aziridin-1-yl)propanoate

Benzyl 3-(aziridin-1-yl)propanoate is an intriguing compound when it comes to solubility characteristics. The solubility of this compound can be influenced by a variety of factors:

  • Polarity: Due to the presence of the aziridine ring, which can enhance polar interactions, the solubility in polar solvents such as water may be limited.
  • Hydrophobic Character: The benzyl group typically contributes a hydrophobic character that can hinder solubility in polar environments.
  • Organic Solvents: It is generally expected to dissolve well in non-polar to moderately polar organic solvents such as dichloromethane, ethyl acetate, or toluene.
  • Temperature: As with many compounds, an increase in temperature might enhance solubility, particularly in organic solvents.

In summary, one might find that "Benzyl 3-(aziridin-1-yl)propanoate" presents varying solubility profiles depending on the solvent system used. The mixture of hydrophobic and polar functionalities can lead to unique behaviors, making it an interesting subject for further study in solubility dynamics.

Interesting facts

Interesting Facts About Benzyl 3-(aziridin-1-yl)propanoate

Benzyl 3-(aziridin-1-yl)propanoate is an intriguing compound that has garnered attention in various fields, particularly in medicinal chemistry and organic synthesis. Below are some fascinating aspects of this chemical:

  • Unique Structure: The presence of the aziridine ring, a three-membered nitrogen-containing heterocycle, imparts unique reactivity and properties to the compound. Aziridines are known for their strain and are often utilized in synthesizing complex molecules.
  • Synthetic Utility: Benzyl 3-(aziridin-1-yl)propanoate serves as a valuable intermediate in organic synthesis. Its ability to participate in various chemical reactions makes it a useful building block for generating diverse chemical entities.
  • Potential Biological Activity: Compounds like benzyl 3-(aziridin-1-yl)propanoate have been explored for their biological activities, which may include antimicrobial and anticancer properties. This opens avenues for research in drug discovery and development.
  • Research Applications: The compound has implications in studying reaction mechanisms, particularly in the field of aziridine chemistry. Its reactions can provide insight into the behavior of similar compounds, enhancing our understanding of chemical reactivity.

In summary, benzyl 3-(aziridin-1-yl)propanoate exemplifies the intersection of interesting structural features and potential applications. It holds promise not only for chemists seeking to innovate in organic synthesis but also for biochemists focusing on developing new therapeutic agents.

As the renowned chemist Robert H. Grubbs once said, “Chemistry is a science of change.” This compound highlights the dynamic nature of chemistry and its endless possibilities.

Synonyms
1-AZIRIDINEPROPIONIC ACID, BENZYL ESTER
1-Aziridinepropanoic acid, benzyl ester
24116-20-9
DTXSID00178839
RefChem:227744
DTXCID10101330