Skip to main content

4-Nitrobenzoyl aziridine

ADVERTISEMENT
Identification
Molecular formula
C9H8N2O3
CAS number
2497-23-6
IUPAC name
aziridin-1-yl-(4-nitrophenyl)methanone
State
State

At room temperature, aziridin-1-yl-(4-nitrophenyl)methanone exists as a solid. The compound remains stable under normal conditions and does not readily sublimate or melt until heated above its melting point.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
192.17g/mol
Molar mass
192.1710g/mol
Density
1.3410g/cm3
Appearence

Aziridin-1-yl-(4-nitrophenyl)methanone is typically a crystalline solid ranging in color from pale yellow to yellow-orange. Its appearance can vary slightly based on purity and environmental conditions such as humidity and temperature.

Comment on solubility

Solubility of Aziridin-1-yl-(4-nitrophenyl)methanone

The solubility of aziridin-1-yl-(4-nitrophenyl)methanone can be described as follows:

  • Polarity: The presence of the nitrophenyl group increases the polarity of the compound, which can affect its solubility profile.
  • Solvents: This compound may show varying solubility in different solvents:
    • Polar solvents, such as water and methanol, could provide enhanced solubility due to interactions between the solvent molecules and the polar nitro group.
    • Non-polar solvents, on the other hand, might result in reduced solubility due to a lack of favorable interactions.
  • Temperature Effects: Generally, increasing temperature tends to increase the solubility of organic compounds. Therefore, experimenting at different temperatures may provide insights into optimal solubility conditions.
  • pH Influence: The solubility may also be affected by the pH of the solution, particularly if the compound can ionize under various pH conditions.

In conclusion, the solubility of aziridin-1-yl-(4-nitrophenyl)methanone is influenced by several factors including polarity, solvent choice, temperature, and pH. Conducting systematic solubility experiments can help to ascertain the most effective conditions for dissolving this compound.

Interesting facts

Interesting Facts About Aziridin-1-yl-(4-nitrophenyl)methanone

Aziridin-1-yl-(4-nitrophenyl)methanone is a fascinating compound that presents unique characteristics and applications in the field of chemistry. Here are some key points that highlight its importance:

  • Structural Features: This compound contains a 5-membered aziridine ring, which is pivotal in organic synthesis due to its reactivity. The presence of a nitrophenyl moiety adds significant polarity, enhancing the compound's versatility in different chemical reactions.
  • Role in Medicinal Chemistry: Compounds that contain aziridine rings are often investigated for their potential in drug development. Aziridinyl derivatives have been noted for acting as *antitumor agents*, contributing to their importance in pharmacology.
  • Synthetic Utility: The compound serves as a valuable intermediate in organic synthesis. Its structure makes it a useful building block for larger, more complex molecules, providing synthetic chemists with a strategic entry point into functionalized compounds.
  • Reactive Behavior: Due to the strain in the aziridine ring, this compound can participate in nucleophilic attacks, making it useful in various reactions such as ring-opening or substitution reactions.
  • Environmental Impact: Understanding the properties and reactions of such compounds is crucial in assessing their environmental safety and toxicity, ensuring that they can be managed appropriately in practical applications.

As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." This resonates particularly well in the context of studying molecules like aziridin-1-yl-(4-nitrophenyl)methanone, which can lead to innovative discoveries across various fields.

In summary, this compound is not just notable for its structure but also for its applications, making it an exciting subject for further research and exploration in the realm of organic chemistry.

Synonyms
1-(p-Nitrobenzoyl)aziridine
N-(p-Nitrobenzoyl)aziridine
p-Nitrobenzoylethyleneimine
Aziridine, 1-(4-nitrobenzoyl)-
1-(4-Nitrobenzoyl)aziridine
AZIRIDINE, 1-(p-NITROBENZOYL)-
19614-29-0
AI3-50751
NSC 50704
BRN 0168173
Y72XXE9V6P
UNII-Y72XXE9V6P
aziridin-1-yl-(4-nitrophenyl)methanone
DTXSID30173276
NSC-50704
NSC50704
SCHEMBL9152022
DTXCID9095767
1-Aziridinyl(4-nitrophenyl)methanone
Aziridine, 1-(4-nitrobenzoyl)-(9CI)
Methanone, 1-aziridinyl(4-nitrophenyl)-