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Aziridine-1-propanoic acid, 2,2,3,3,4,4,4-heptafluorobutyl ester

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Identification
Molecular formula
C7H7F7NO2
CAS number
62211-93-0
IUPAC name
2,2,3,3,4,4,4-heptafluorobutyl 3-(aziridin-1-yl)propanoate
State
State

The compound is a liquid at room temperature, exhibiting a clear and colorless appearance. Its liquid state is evident due to its boiling point being significantly above room temperature.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
158.00
Boiling point (Kelvin)
431.15
General information
Molecular weight
281.14g/mol
Molar mass
281.1440g/mol
Density
1.5550g/cm3
Appearence
This compound typically presents as a clear liquid. Its appearance is characterized by a lack of color, akin to water or other similar transparent, colorless liquids.
Comment on solubility

Solubility of 2,2,3,3,4,4,4-heptafluorobutyl 3-(aziridin-1-yl)propanoate

The solubility of 2,2,3,3,4,4,4-heptafluorobutyl 3-(aziridin-1-yl)propanoate is quite intriguing due to its unique structure and functional groups. This compound contains both fluoroalkyl and aziridine functionalities, leading to distinct interactions with solvents:

  • Polarity: The presence of multiple fluorine atoms enhances the compound's polarity, which can significantly affect its solubility in different solvents.
  • Hydrophobic Characteristics: The heptafluorobutyl group tends to be hydrophobic, suggesting poor solubility in water yet potentially better solubility in organic solvents.
  • Solvent Compatibility: It is likely to be soluble in low-polarity solvents, such as chloroform or ethyl acetate, while showing negligible solubility in highly polar solvents.

In practical terms, it is crucial to consider the solvent environment when assessing the solubility of this compound. As stated, "like dissolves like," meaning that nonpolar solvents will better accommodate this compound compared to polar solvents.

Overall, the chemical's solubility properties make it a subject of interest for various applications, especially in fields requiring specific solvent interactions. Further studies may clarify its solubility behaviors in more complex media.

Interesting facts

Interesting Facts about 2,2,3,3,4,4,4-heptafluorobutyl 3-(aziridin-1-yl)propanoate

This intriguing compound is a fascinating example of how fluorinated molecules can significantly alter the properties and reactivity of organic compounds. Here are some compelling highlights:

  • Fluorination Paradigm: The presence of fluorine atoms in its structure provides unique characteristics, such as enhanced stability and special interactions with biological systems.
  • Aziridine Moiety: The compound includes an aziridine ring, a three-membered cyclic amine that is known for its strain and reactivity. This makes it a building block for various synthetic applications.
  • Medicinal Chemistry: Compounds like this one are often investigated for their potential use in medicinal applications, especially in designing drug candidates that might interact with biological molecules in innovative ways.
  • Synthetic Utility: The structural components allow for versatile synthetic transformations, making it a valuable intermediate in chemical synthesis.
  • Environmental Considerations: Fluorinated compounds are of interest not just for their chemical properties but also for their environmental impact. Understanding the fate and transport of such compounds is crucial for environmental chemistry.

Overall, 2,2,3,3,4,4,4-heptafluorobutyl 3-(aziridin-1-yl)propanoate serves as a prime example of the intersection between organic chemistry and practical applications in materials science and medicinal development. Its study could yield valuable insights into both fundamental chemistry and real-world applications.

Synonyms
24160-20-1
1-AZIRIDINEPROPIONIC ACID, 2,2,3,3,4,4,4-HEPTAFLUOROBUTYL ESTER
1-Aziridinepropanoic acid, 2,2,3,3,4,4,4-heptafluorobutyl ester
DTXSID60178870
RefChem:227740
DTXCID20101361
NS00110859