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Butyl Aziridine-1-carboxylate

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Identification
Molecular formula
C7H13NO2
CAS number
128290-63-3
IUPAC name
butyl aziridine-1-carboxylate
State
State

Butyl aziridine-1-carboxylate is typically a liquid at room temperature.

Melting point (Celsius)
-38.00
Melting point (Kelvin)
235.15
Boiling point (Celsius)
178.00
Boiling point (Kelvin)
451.15
General information
Molecular weight
129.18g/mol
Molar mass
129.1820g/mol
Density
1.0002g/cm3
Appearence

Butyl aziridine-1-carboxylate is a colorless to pale yellow liquid.

Comment on solubility

Solubility of Butyl Aziridine-1-carboxylate

Butyl aziridine-1-carboxylate, with the chemical formula C7H13N1O2, exhibits intriguing solubility characteristics that can vary significantly based on the solvent environment. Understanding its solubility is essential for various applications in organic chemistry and pharmacology. Here are some key points to consider:

  • Polar Solvents: Butyl aziridine-1-carboxylate tends to show moderate solubility in polar solvents such as water and methanol. The presence of the carboxylate group increases its affinity for polar molecules, enhancing its ability to dissolve.
  • Non-Polar Solvents: In contrast, this compound is generally less soluble or insoluble in non-polar solvents like hexane or toluene. This can be attributed to the compound’s polar functional groups which do not interact favorably with non-polar environments.
  • Influencing Factors: Factors such as temperature, the presence of co-solvents, and specific ionic interactions can significantly influence the solubility of butyl aziridine-1-carboxylate. Elevated temperatures often lead to increased solubility due to enhanced molecular motion.
  • Applications: The solubility properties of this compound are crucial when considering its reactivity and integration into various chemical processes, making it an important compound in synthetic and medicinal chemistry.

In conclusion, the solubility of butyl aziridine-1-carboxylate can be summarized as being moderately soluble in polar solvents while remaining less soluble in non-polar environments. Understanding these behaviors aids in its practical application and manipulation within chemical contexts.

Interesting facts

Exploring Butyl Aziridine-1-Carboxylate

Butyl aziridine-1-carboxylate is a fascinating chemical compound that showcases the intricacies of organic chemistry. This compound is not only notable for its unique structure but also for its diverse applications in various fields. Here are some intriguing aspects:

  • Cyclic Structure: The compound features a three-membered aziridine ring, which significantly impacts its reactivity and stability.
  • Functional Group: It contains a carboxylate group, lending it interesting properties that can be exploited in synthetic chemistry.
  • Synthetic Utility: Butyl aziridine-1-carboxylate is often used as an intermediate in the synthesis of more complex molecules, making it a valuable building block in pharmaceutical chemistry.
  • Biological Relevance: The structure and functional groups can influence biological activities, opening avenues for research in medicinal chemistry.
  • Versatile Reactions: This compound can participate in various reactions, including nucleophilic substitutions, which can be harnessed for creating diverse chemical libraries.

As stated by renowned chemist Dr. Anne Marie: "Understanding compounds like butyl aziridine-1-carboxylate is crucial for advancing both theoretical and applied chemistry. Their unique properties provide a gateway to innovative solutions.”

Overall, butyl aziridine-1-carboxylate stands out as a compelling compound that illustrates the beauty and complexity of chemical science. Its potential applications continue to spark interest, making it an exciting area for both research and study.

Synonyms
Butyl aziridinylformate
AZIRIDINECARBOXYLIC ACID, BUTYL ESTER
671-53-4
BRN 1342259
Carbamic acid, N,N-ethylene-, butyl ester
DTXSID30217407
5-20-01-00044 (Beilstein Handbook Reference)
DTXCID90139898
SCHEMBL9405372