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1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone

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Identification
Molecular formula
C12H13N3O3
CAS number
1068-90-2
IUPAC name
1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone
State
State

At room temperature, 1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone is typically a solid.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
365.15
Boiling point (Kelvin)
638.30
General information
Molecular weight
233.26g/mol
Molar mass
233.2630g/mol
Density
1.3446g/cm3
Appearence

The compound appears as a crystalline solid with a yellowish to light brown color.

Comment on solubility

Solubility of 1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone

The solubility of 1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone in various solvents is an area of particular interest due to its potential applications in pharmacology and organic synthesis.

When assessing the solubility characteristics of this compound, several factors should be considered:

  • Polarity: The presence of both the nitrophenyl and pyrrolidine groups in the structure often influences solubility, especially in polar solvents like water and alcohols.
  • Solvent Interactions: 1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone may have limited solubility in non-polar solvents due to the relatively polar nature of the functional groups.
  • Temperature Dependence: Like many organic compounds, solubility can improve with increased temperature, making higher temperatures potentially beneficial for dissolving this compound.

In general, it is essential to conduct experimental assessments to determine its precise solubility profile. Understanding these solubility properties is crucial for effective formulation in various applications.

Interesting facts

Exploring 1-(4-Nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone

1-(4-Nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone is a fascinating compound that can be appreciated for its unique structural characteristics and potential applications in science.

Key Features

  • Structural Diversity: The compound features a pyrrolidine ring, which is a five-membered ring containing nitrogen. This type of structure is known for its presence in various alkaloids and pharmaceuticals.
  • Nitrophenyl Group: The presence of a nitrophenyl group introduces electron-withdrawing characteristics that can influence reactivity and solubility, paving the way for interesting reaction pathways.

Applications & Significance

The intriguing properties of 1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone make it noteworthy in various fields:

  • Pharmaceutical Chemistry: Due to its unique functional groups, there is potential for this compound to act as a lead or intermediate in drug development. Compounds featuring similar motifs are often explored for their biological activity.
  • Research in Organic Synthesis: As a nitrogen-containing compound, it can be of interest in synthetic organic chemistry, particularly in the synthesis of more complex molecules.

Research Potential

This compound’s reactivity highlights its potential as a subject for research in:

  • Catalysis: It might serve as a catalyst or a precursor in various chemical reactions.
  • Material Science: Its derivatives could be investigated for their utility in developing innovative materials like polymers or advanced coatings.

As we broaden our understanding of such compounds, we can unlock not only their chemical potential but also their contributions to technology and medicine. In the words of chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Exploring compounds like 1-(4-nitrophenyl)-2-pyrrolidin-1-ylimino-ethanone contributes to this wealth of ideas in the field of chemistry.