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Vinyl phthalimidoacetate

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Identification
Molecular formula
C12H9NO4
CAS number
55715-79-0
IUPAC name
vinyl 2-(1,3-dioxoisoindolin-2-yl)acetate
State
State

The compound is typically a solid at room temperature.

Melting point (Celsius)
60.00
Melting point (Kelvin)
333.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
231.22g/mol
Molar mass
231.2170g/mol
Density
1.2500g/cm3
Appearence

Vinyl phthalimidoacetate typically appears as a solid crystal or powder. Its color can range from white to off-white, depending on the specific purity and conditions of the compound.

Comment on solubility

Solubility of Vinyl 2-(1,3-Dioxoisoindolin-2-yl)acetate

Understanding the solubility of vinyl 2-(1,3-dioxoisoindolin-2-yl)acetate is essential for various applications, especially in synthetic organic chemistry. This compound presents an intriguing profile when it interacts with solvents due to its structural features.

General Solubility Characteristics:

  • Polar Solvents: The presence of functional groups may suggest some degree of solubility in polar solvents, such as water and ethanol.
  • Non-Polar Solvents: In contrast, non-polar solvents like hexane may show limited solubility due to the compound's functional characteristics.
  • pH Sensitivity: The solubility might vary with changes in pH, impacting the ionization of any acidic or basic groups present in the structure.

To summarize, the solubility of vinyl 2-(1,3-dioxoisoindolin-2-yl)acetate can be inferred as being generally moderate in polar solvents, while demonstrating limited solubility in non-polar environments. This behavior reflects the compound's unique chemical characteristics, making it essential to test solubility in specific conditions relevant to the intended application.

Interesting facts

Interesting Facts about Vinyl 2-(1,3-Dioxoisoindolin-2-yl)acetate

Vinyl 2-(1,3-dioxoisoindolin-2-yl)acetate is a fascinating compound with interesting properties and applications. Here are some key points to consider:

  • Structural Complexity: This compound contains a unique isoindoline core, which is notable for its presence in various natural products and pharmaceuticals. The combination of a vinyl group with dioxoisoindoline makes it potentially valuable in synthetic chemistry.
  • Potential Applications: Due to its structural composition, this compound may be explored for use in:
    • Organic synthesis, where building blocks are needed for complex molecules
    • Pharmaceuticals, particularly in the development of drugs targeting certain biological pathways
    • Material science, where compounds can serve as precursors for polymers or functional materials
  • Reaction Mechanisms: The vinyl group makes this compound a participant in numerous reactions such as polymerization and cross-coupling reactions, expanding its utility in the lab.
  • Research Interest: Scientists are investigating variations of isoindoline derivatives, inspiring ongoing research into their medicinal properties. Many studies cite their potential antitumor and antimicrobial activities.
  • Historical Significance: Isoindoline derivatives have been known and studied for decades, contributing to our understanding of heterocyclic chemistry.

In summary, vinyl 2-(1,3-dioxoisoindolin-2-yl)acetate presents a rich platform for scientific exploration. Its chemical architecture offers intriguing avenues for research in both practical and theoretical realms.

Synonyms
2756-76-5
1,3-Dioxo-2-isoindolineacetic acid vinyl ester
2-ISOINDOLINEACETIC ACID, 1,3-DIOXO-, VINYL ESTER
4L55VYA8S2
N-Phthaloylglycine vinyl ester
BRN 0211739
UNII-4L55VYA8S2
5-21-10-00432 (Beilstein Handbook Reference)
DTXSID20181961