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Acetoxyfuranone

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Identification
Molecular formula
C10H8O7
CAS number
132-64-9
IUPAC name
(4-acetoxy-2,5-dioxo-3-furyl) acetate
State
State

At room temperature, the compound is a solid. It is generally stable under standard conditions.

Melting point (Celsius)
80.00
Melting point (Kelvin)
353.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
216.16g/mol
Molar mass
216.1560g/mol
Density
1.3768g/cm3
Appearence

(4-acetoxy-2,5-dioxo-3-furyl) acetate is typically a white to pale yellow solid powder. It generally appears as a fine crystallized substance.

Comment on solubility

Solubility of (4-acetoxy-2,5-dioxo-3-furyl) acetate

(4-acetoxy-2,5-dioxo-3-furyl) acetate, known for its unique structure, exhibits intriguing solubility characteristics. Its solubility profile can be influenced by several factors, including the presence of polar groups and the overall molecular structure.

When considering the solubility of this compound, several key points can be highlighted:

  • Polar Nature: The presence of the acetoxy group contributes to potential interactions with polar solvents such as water, possibly enhancing solubility in these environments.
  • Solvent Dependency: Solubility may vary significantly based on the solvent used. It is likely to be more soluble in organic solvents like ethanol or acetone compared to non-polar solvents.
  • Temperature Effects: As with many compounds, solubility could increase with temperature, allowing greater dissolution in the chosen solvent.
  • Structural Effects: The dioxo structure may affect the intermolecular forces, playing a role in the overall solubility behavior.

To summarize, the solubility of (4-acetoxy-2,5-dioxo-3-furyl) acetate is influenced by its polar functional groups and environmental conditions. As with many organics, experimenting with various solvents and temperatures can help uncover the most effective solubility conditions for practical applications.

Interesting facts

Interesting Facts about (4-acetoxy-2,5-dioxo-3-furyl) acetate

(4-acetoxy-2,5-dioxo-3-furyl) acetate presents a fascinating composition of functional groups that highlights the intricate world of organic chemistry. This compound belongs to the furan family and showcases some unique properties that make it significant in various applications.

Chemical Significance

This compound is particularly interesting due to its incorporation of both furan and acetate functionalities, contributing to its reactivity and potential utility. Here are some noteworthy aspects:

  • Versatility: The furan ring structure is known for its aromatic properties, making it a highly valuable scaffold in organic synthesis.
  • Reactivity: The presence of multiple carbonyl groups (dioxo) allows this compound to participate in numerous chemical reactions, including nucleophilic additions and inter-conversion under various conditions.
  • Biological Interest: Compounds containing furan rings are often studied for their biological activity, leading to potential pharmaceuticals or agrochemicals.

Applications and Research

Among its various applications, (4-acetoxy-2,5-dioxo-3-furyl) acetate can be used in:

  • Synthesis: Acts as an intermediate in organic synthesis, potentially leading to the development of more complex molecules.
  • Material Science: The compound is a candidate for creating new materials with unique properties.
  • Pharmaceutical Research: Initial studies may indicate the compound's role in medicinal chemistry for developing new drug candidates.

Quote to Ponder

As Albert Szent-Györgyi once stated, "Discovery consists of looking at the same thing as everyone else and thinking something different." This sentiment rings true in the study of compounds like (4-acetoxy-2,5-dioxo-3-furyl) acetate, where a different perspective can unveil extraordinary insights and opportunities for innovation.

In summary, the compound (4-acetoxy-2,5-dioxo-3-furyl) acetate exemplifies the beauty of chemistry through its diverse functions and potential applications. By unlocking the secrets of such compounds, scientists can pave the way for advancements across various fields.

Synonyms
132-79-6
2,5-dioxo-2,5-dihydrofuran-3,4-diyl diacetate
Dihydroxymaleic anhydride diacetate
BRN 0214116
MALEIC ANHYDRIDE, DIHYDROXY-, DIACETATE
DTXSID90927494