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Isopropyl aziridine-1-carboxylate

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Identification
Molecular formula
C6H11NO2
CAS number
1193-20-6
IUPAC name
isopropyl aziridine-1-carboxylate
State
State

This compound is a liquid at room temperature.

Melting point (Celsius)
-72.00
Melting point (Kelvin)
201.15
Boiling point (Celsius)
154.00
Boiling point (Kelvin)
427.15
General information
Molecular weight
129.16g/mol
Molar mass
129.1560g/mol
Density
0.9938g/cm3
Appearence

Isopropyl aziridine-1-carboxylate appears as a colorless to pale yellow liquid. It may have a faintly sweet or ammonia-like odor, typical of ester compounds.

Comment on solubility

Solubility of Isopropyl Aziridine-1-Carboxylate

Isopropyl aziridine-1-carboxylate, a compound featuring the aziridine functional group, presents an intriguing profile when it comes to solubility. Understanding its solubility characteristics is essential for both practical applications and theoretical studies.

Key Points on Solubility:

  • Polarity: The presence of the carboxylate functional group suggests that isopropyl aziridine-1-carboxylate may exhibit moderate polarity, which often enhances its solubility in polar solvents.
  • Solvent Interaction: It is likely to be soluble in polar solvents such as water, ethanol, and acetone, due to the ability of the carboxylate group to engage in hydrogen bonding.
  • Lower Solubility in Non-Polar Solvents: Conversely, one might observe lower solubility levels in non-polar solvents such as hexane and benzene, reflecting its chemical structure and polarity.
  • Concentration Effects: The degree of solubility can vary based on concentration, temperature, and other environmental factors, highlighting an essential consideration in experimental setups.

In summary, the solubility behavior of isopropyl aziridine-1-carboxylate can be effectively summarized by its interaction with different solvents, particularly how structural features like the carboxylate group influence its affinity for polar versus non-polar media. Hence, it is crucial to consider these factors when handling this compound in various chemical contexts.

Interesting facts

Interesting Facts about Isopropyl Aziridine-1-Carboxylate

Isopropyl aziridine-1-carboxylate is a fascinating compound that belongs to the class of aziridine derivatives, which are small, three-membered nitrogen-containing heterocycles. These compounds are of significant interest in the realm of synthetic chemistry due to their unique structural properties and reactivity. Here are some engaging facts about this compound:

  • Versatile Building Blocks: Aziridines, including isopropyl aziridine-1-carboxylate, serve as important intermediates in the synthesis of various bioactive molecules and pharmaceuticals.
  • Chirality and Stereochemistry: The presence of a carboxylate group introduces chirality, allowing for the formation of enantiomerically pure compounds, which can exhibit different biological activities.
  • Applications in Drug Development: Compounds like isopropyl aziridine-1-carboxylate have potential applications in medicinal chemistry, particularly in the development of new drugs targeting specific diseases.
  • Ring Strain: The three-membered ring structure of aziridines imparts significant ring strain, making them highly reactive. This feature is often exploited in synthetic routes to facilitate ring-opening reactions.
  • Catalytic Reactions: Isopropyl aziridine-1-carboxylate can be used in various catalytic reactions, expanding its utility in organic synthesis and potentially leading to novel reaction pathways.

As a scientist or a chemistry student, exploring the reactivity and applications of isopropyl aziridine-1-carboxylate can unveil a world of possibilities in synthetic chemistry. Its intriguing structure and properties make it an exciting subject of study that continues to captivate researchers worldwide.

Synonyms
Isopropyl aziridinylformate
AZIRIDINECARBOXYLIC ACID, ISOPROPYL ESTER
671-52-3
Carbamic acid, N,N-ethylene-, isopropyl ester
1-Aziridinecarboxylic acid, 1-methylethyl ester
DTXSID70217406
DTXCID30139897
1-Aziridinecarboxylic acid, 1-methylethyl ester (9CI)
propan-2-yl aziridine-1-carboxylate