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Sec-butyl 3-(aziridin-1-yl)propanoate

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Identification
Molecular formula
C9H17NO2
CAS number
. DNA0297444
IUPAC name
sec-butyl 3-(aziridin-1-yl)propanoate
State
State

At room temperature, the compound is typically a liquid. It is often handled under standard laboratory conditions.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
247.00
Boiling point (Kelvin)
520.15
General information
Molecular weight
185.27g/mol
Molar mass
185.2710g/mol
Density
1.0150g/cm3
Appearence

Sec-butyl 3-(aziridin-1-yl)propanoate appears as a colorless to pale yellow liquid. It may have a faint, characteristic odor.

Comment on solubility

Solubility of sec-butyl 3-(aziridin-1-yl)propanoate

Sec-butyl 3-(aziridin-1-yl)propanoate presents interesting solubility characteristics that emerge from its molecular structure. As an ester, it has the potential for varied solubility in different solvents based on its polarity and functional groups:

  • Nonpolar Solvents: Compounds with hydrocarbon chains, like sec-butyl, tend to be more soluble in nonpolar solvents such as hexane or toluene. This is due to the hydrophobic nature of the alkyl group.
  • Polar Solvents: Conversely, when in contact with polar solvents (like water), the solubility may decrease. This is a result of the weaker interactions between polar solvent molecules and the somewhat polar group from the aziridine moiety.
  • Temperature Effects: Solubility can also vary significantly with temperature. Higher temperatures often lead to increased solubility due to enhanced molecular movement.
  • pH Influence: The acidity or basicity of the solvent can further influence solubility, especially if the compound has functional groups that can ionize.

In summary, the solubility of sec-butyl 3-(aziridin-1-yl)propanoate is a complex interplay of various factors, including molecular structure, solvent characteristics, and environmental conditions. As such, understanding these influences can facilitate its practical applications in fields such as organic synthesis and medicinal chemistry.

Interesting facts

Interesting Facts about sec-butyl 3-(aziridin-1-yl)propanoate

sec-butyl 3-(aziridin-1-yl)propanoate is a fascinating compound with unique characteristics and applications. Here are some intriguing facts about it:

  • Structure and Reactivity: The presence of an aziridine ring, a three-membered nitrogen-containing heterocycle, lends this compound interesting reactivity patterns. Aziridines can easily undergo ring-opening reactions, which makes them valuable intermediates in organic synthesis.
  • Applications in Medicinal Chemistry: Compounds bearing aziridine functionalities are often explored for their potential pharmacological activities. They may act as building blocks for the development of novel therapeutic agents, particularly in cancer treatment.
  • Chirality: The presence of the sec-butyl group introduces a chiral center in the molecule, enhancing its importance in studies of stereochemistry and chiral synthesis. This property is crucial for its biological activities, as different enantiomers can exhibit different biological effects.
  • Polymer Chemistry: Due to its ability to participate in various polymerization processes, sec-butyl 3-(aziridin-1-yl)propanoate can be utilized in the creation of advanced materials, including adhesives and coatings. The diversity in its applications showcases its versatility.
  • Research Potential: As a compound with emerging importance, there is ongoing research aimed at exploring its characteristics and expanding its applications in fields such as nanotechnology and drug delivery systems.

In conclusion, sec-butyl 3-(aziridin-1-yl)propanoate represents a compelling subject of study in the realm of organic chemistry. Its structural features and potential applications make it a significant compound in both academic and industrial settings.

Synonyms
1-AZIRIDINEPROPIONIC ACID, sec-BUTYL ESTER
23693-84-7
RefChem:1054900
Aziridine propionic acid, sec-butyl ester
butan-2-yl 3-(aziridin-1-yl)propanoate
1-Aziridinepropanoic acid, sec-butyl ester
DTXSID20946496