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Fumaric acid dimethyl ester

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Identification
Molecular formula
C8H10O4
CAS number
624-49-7
IUPAC name
but-2-enoyl but-2-enoate
State
State
Solid at room temperature; it transitions into a liquid when heated close to its melting point.
Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
194.20
Boiling point (Kelvin)
467.35
General information
Molecular weight
172.17g/mol
Molar mass
172.1500g/mol
Density
1.1800g/cm3
Appearence

Fumaric acid dimethyl ester is typically a colorless, crystalline solid. It is a diester derived from fumaric acid, and its crystalline nature leads to a clear, glass-like appearance.

Comment on solubility

Solubility of But-2-enoyl but-2-enoate

But-2-enoyl but-2-enoate, also known as a type of unsaturated ester, exhibits unique solubility characteristics due to its molecular structure. Its solubility is influenced by several factors, including the presence of the butenyl groups and the polar character of the ester functional group.

Solubility Characteristics:

  • Solvent Preference: But-2-enoyl but-2-enoate is generally more soluble in organic solvents such as ethanol, methanol, and other polar organic solutions than in water.
  • Temperature Influence: Increased temperatures can enhance solubility, promoting better dissolution in solvents. This is typical for many organic compounds.
  • Concentration Effects: At higher concentrations, the solubility may lead to significant solvation interactions, which can alter the viscosity of the solution.
  • Structural Roles: The double bonds present in but-2-enoyl but-2-enoate can help increase intermolecular interactions with other organic compounds, potentially forming more soluble complexes.

Overall, understanding the solubility of but-2-enoyl but-2-enoate is crucial for its applications in various fields, such as polymer chemistry and pharmaceuticals. It is essential to consider these factors when selecting solvents for reactions or formulations involving this compound.

Interesting facts

Interesting Facts about But-2-enoyl but-2-enoate

But-2-enoyl but-2-enoate, also known as a type of ester, is a fascinating compound with a variety of applications and unique properties that make it a worthy subject of study within the realm of organic chemistry. Here are some interesting aspects to consider:

  • Application in Synthetic Chemistry: This compound can be used as an intermediate in the synthesis of larger, more complex molecules. Its functional groups provide a reactive building block in various organic reactions.
  • Role in Polymers: Esters, including but-2-enoyl but-2-enoate, are significant in the production of polymers. They can be incorporated into synthetic pathways to create materials with specific characteristics.
  • Potential in Food Chemistry: Compounds resembling but-2-enoyl but-2-enoate can mimick flavor profiles in food chemistry, leading to interest in how they can enhance or replace synthetic flavors, making them suitable for food applications.
  • Environmental Considerations: Understanding the degradation pathways of esters contributes to better pollution management strategies, as these compounds can release harmful products under certain conditions.
  • Research Frontier: Ongoing studies focus on the role of similar compounds in various fields such as material sciences and medicinal chemistry, exemplifying how esters can bridge multiple disciplines.

As noted by renowned chemists, “The complexity of organic compounds is often an outward reflection of the intricate environments in which they found their place.” This sentiment resonates strongly with but-2-enoyl but-2-enoate, highlighting its significance beyond mere molecular structure.

Overall, but-2-enoyl but-2-enoate represents a compelling intersection of practicality and chemical intricacy, serving as a reminder of the diverse roles organic compounds play in both nature and technology.

Synonyms
But-2-enoic anhydride
but-2-enoyl but-2-enoate
2-Butenoic acid anhydride
Butensaureanhydrid
2-Butenoic acid, anhydride, (2E,2'E)-
SCHEMBL3259515
DTXSID10870711
VJDDQSBNUHLBTD-UHFFFAOYSA-N
AKOS025244034
DB-054144
NS00043849