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1-(Aziridin-1-yl)allyl acetate

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Identification
Molecular formula
C7H11NO2
CAS number
35223-80-4
IUPAC name
1-(aziridin-1-yl)allyl acetate
State
State

This compound is in a liquid state at room temperature.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
188.00
Boiling point (Kelvin)
461.15
General information
Molecular weight
141.18g/mol
Molar mass
141.1840g/mol
Density
1.0124g/cm3
Appearence

The compound is typically a colorless to pale-yellow liquid with a distinct chemical odor. It is transparent and can be slightly viscous.

Comment on solubility

Solubility of 1-(aziridin-1-yl)allyl acetate

The solubility of 1-(aziridin-1-yl)allyl acetate can be characterized by several key factors that highlight its behavior in various solvents.

  • Polarity: The presence of the acetate group contributes significantly to the overall polarity of the compound, which may enhance its solubility in polar solvents like water and alcohol.
  • Organic Solvents: This compound is likely to exhibit higher solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and acetone, owing to its non-polar aziridine ring.
  • Temperature Dependence: As with many chemical compounds, solubility may increase with temperature, making it essential to consider temperature control when working with this substance.

Users often report, "The solubility of 1-(aziridin-1-yl)allyl acetate in diverse environments varies, reflecting its unique chemical structure." Therefore, it is advisable to perform solubility tests in various solvents under different conditions to precisely determine the optimal solvent for specific applications.

In summary: To ensure successful application and handling of 1-(aziridin-1-yl)allyl acetate, one should explore its solubility in both polar and non-polar solvents while considering factors such as temperature and solvent composition.

Interesting facts

Interesting Facts about 1-(Aziridin-1-yl)allyl Acetate

1-(Aziridin-1-yl)allyl acetate is a fascinating compound that showcases the unique properties and reactivity associated with aziridine derivatives. Aziridine, a three-membered nitrogen-containing heterocycle, often contributes to the intriguing behavior of compounds in the realm of organic chemistry.

Key Features

  • Reactivity: The aziridine ring provides a strain that makes compounds like 1-(aziridin-1-yl)allyl acetate particularly reactive. This reactivity is beneficial in synthetic chemistry, allowing for various transformations.
  • Synthesis: The compound can be synthesized through nucleophilic substitutions or through the reaction of aziridines with allyl acetates. This contributes to its importance in developing new organic compounds.
  • Biological Activity: Many aziridine-containing compounds have demonstrated interesting biological properties, which can include antimicrobial and anti-cancer activities, making them potential candidates for drug development.
  • Applications: Beyond biological applications, it can also serve as an important building block in the synthesis of complex organic molecules, particularly in the pharmaceutical industry.

Fun Fact

Due to the unique structure of aziridine, the reactivity of 1-(aziridin-1-yl)allyl acetate can lead to the formation of various new compounds via ring-opening reactions, making it a valuable intermediate in organic synthesis. This compound reminds us of the beauty and complexity found in chemical structures and their transformations!

Synonyms
1-(aziridin-1-yl)prop-2-enyl acetate
22204-42-8
DTXSID10274912