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2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate

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Identification
Molecular formula
C10H18N2O2
CAS number
76545-57-6
IUPAC name
2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate
State
State

At room temperature, 2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate is usually in a liquid state. This compound's state is due to its molecular structure and relatively low melting point, which is below room temperature.

Melting point (Celsius)
-18.00
Melting point (Kelvin)
255.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
199.27g/mol
Molar mass
199.2680g/mol
Density
1.0368g/cm3
Appearence

2-(Dimethylamino)ethyl 3-(aziridin-1-yl)propanoate is typically a liquid due to its ester composition. The compound is often observed as a colorless to pale yellow liquid, providing an indication of its purity and age. The appearance may slightly vary based on specific conditions and impurities present during synthesis.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate

The solubility of 2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate in various solvents reveals intriguing insights into its behavior in solution. This compound's solubility can be influenced by several factors, including:

  • Polarity: Due to the presence of both polar (dimethylamino) and non-polar regions (the aziridine ring), this compound is expected to exhibit moderate solubility in polar solvents like water and alcohols.
  • Temperature: As the temperature increases, solubility can also increase. This is crucial for reactions involving this compound, as higher temperatures may promote dissolution.
  • pH Levels: The compound is likely to show better solubility in basic conditions because the dimethylamino group can become protonated, increasing overall solubility in aqueous environments.

Furthermore, it is important to note the **thermodynamic properties** at play. For instance, if one were to state that "the solubility increases as the energy of solvation becomes favorable," it encapsulates the core concept of solubility dynamics.

In conclusion, solubility is pivotal for understanding the reactivity and application of 2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate, as it affects its interaction in chemical reactions and potential usage in pharmaceutical contexts. Understanding these solubility characteristics can greatly enhance the compound’s applicability in different scientific fields.

Interesting facts

Interesting Facts about 2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate

2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate is a fascinating compound that showcases the intricate world of organic chemistry, particularly its applications in medicinal chemistry and drug design. This compound is notable for several reasons:

  • Biological Activity: This compound is often explored for its potential applications in pharmaceuticals, especially as it features both an aziridine ring, known for its reactivity in biological systems, and a dimethylamino group that can enhance its pharmacological profile.
  • Versatile Synthesis: The synthesis of this compound typically involves multi-step synthetic routes that highlight the creativity and ingenuity required in organic chemistry. This can open up discussions about various synthetic pathways and strategies used in complex molecule design.
  • Reactive Intermediate: The presence of the aziridine moiety allows it to act as a reactive intermediate, providing a springboard for further chemical reactions. This can lead to various derivative compounds, making it an attractive target for research and development.
  • Potential in Cancer Research: Compounds like this one are often investigated for their capabilities in targeting cancer cells. The aziridine group can participate in mechanisms that disrupt cellular functions in malignancy, making it a topic of interest in cancer therapy.

In conclusion, the exploration of 2-(dimethylamino)ethyl 3-(aziridin-1-yl)propanoate not only emphasizes the importance of organic compounds in modern science but also showcases the remarkable interplay between structure and function in drug discovery. As researchers delve deeper into its properties and potential uses, we can anticipate exciting developments in the fields of pharmacology and medicinal chemistry.

Synonyms
1-AZIRIDINEPROPIONIC ACID, 2-(DIMETHYLAMINO)ETHYL ESTER
22480-26-8
Q1KT4R5DR8
NSC 101302
1-Aziridinepropanoic acid, 2-(dimethylamino)ethyl ester
UNII-Q1KT4R5DR8
NSC-101302
DTXSID80177007
RefChem:74941
DTXCID5099498
NCIOpen2_001749
NSC101302