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N-Vinylsuccinimide

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Identification
Molecular formula
C6H7NO2
CAS number
6308-22-5
IUPAC name
1-vinylpyrrole-2,5-dione
State
State

At room temperature, N-Vinylsuccinimide is generally solid and can sometimes appear as a crystalline powder.

Melting point (Celsius)
74.50
Melting point (Kelvin)
347.65
Boiling point (Celsius)
228.00
Boiling point (Kelvin)
501.15
General information
Molecular weight
111.13g/mol
Molar mass
111.1130g/mol
Density
1.2430g/cm3
Appearence

N-Vinylsuccinimide appears as a colorless to pale yellow crystalline solid. It may also be found as a powder and can be hygroscopic, meaning it may absorb moisture from the air.

Comment on solubility

Solubility of 1-vinylpyrrole-2,5-dione

1-vinylpyrrole-2,5-dione, known for its unique structural features, presents interesting characteristics regarding its solubility. Understanding the solubility of this compound is essential for its applications in various fields.

Key Points on Solubility:

  • Solvents: 1-vinylpyrrole-2,5-dione is generally soluble in polar solvents such as water, methanol, and ethanol due to its ability to form hydrogen bonds.
  • Temperature Effects: Its solubility can increase at elevated temperatures. As with many organic compounds, heat can enhance interaction with the solvent.
  • pH Dependence: The solubility may also vary with changes in pH, as certain functional groups can become protonated or deprotonated, affecting solubility.

Overall, the solubility of 1-vinylpyrrole-2,5-dione reflects its chemical nature, making it a vital compound for researchers and industry professionals alike. As one source aptly notes, "the solubility behavior of compounds can dictate their usefulness in practical applications."

In summary, the solubility profile of 1-vinylpyrrole-2,5-dione highlights the interplay between molecular structure and solvent environment, underscoring the importance of solvent selection in chemical processes.

Interesting facts

Interesting Facts about 1-vinylpyrrole-2,5-dione

1-vinylpyrrole-2,5-dione is a fascinating compound within the realm of organic chemistry, particularly notable for its role in various synthetic applications. Here are some intriguing insights:

  • Versatile Reactivity: This compound can act as a versatile building block in organic synthesis, enabling chemists to create complex molecules through various reactions, including polymerization.
  • Electrophilic Substitution: Its unique structure allows for electrophilic substitution reactions, making it a valuable intermediate in producing more complex structures.
  • Biocompatibility: Research has shown that it can potentially be used in biocompatible materials, leading to applications in biomedical fields.
  • Research Applications: It is extensively studied in the field of materials science, especially for its properties in creating conductive polymers.
  • Quinonoid Character: As a quinonoid compound, 1-vinylpyrrole-2,5-dione exhibits interesting electronic properties that can be manipulated for various applications.

Overall, 1-vinylpyrrole-2,5-dione not only stands as an important compound in academic research but also opens doors for innovative applications across chemistry and material science. As the field evolves, it is likely that new uses of this compound will continue to emerge, highlighting its significance in contemporary chemical research.

Synonyms
1-ethenylpyrrole-2,5-dione
7685-94-1
MALEIMIDE, N-VINYL-
1H-Pyrrole-2,5-dione, 1-ethenyl-
1-ethenyl-2,5-dihydro-1h-pyrrole-2,5-dione
N-Vinylmaleimide
1-Vinyl-1H-pyrrole-2,5-dione
SCHEMBL1664700
DTXSID10227660
KZCSJWFLPQFDNW-UHFFFAOYSA-N
1-Vinyl-1H-pyrrole-2,5-dione #
G50126
EN300-6759199
Z2375614796