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bromophenyl maleate

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Identification
Molecular formula
C11H8BrNaO4
CAS number
63932-82-7
IUPAC name
sodium;3-bromo-4-(4-methoxyphenyl)-4-oxo-but-2-enoate
State
State

At room temperature, bromophenyl maleate is a solid.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
320.13g/mol
Molar mass
320.1320g/mol
Density
1.5000g/cm3
Appearence

Bromophenyl maleate appears as a white crystalline powder.

Comment on solubility

Solubility of Sodium 3-Bromo-4-(4-Methoxyphenyl)-4-Oxo-But-2-Enoate

Sodium 3-bromo-4-(4-methoxyphenyl)-4-oxo-but-2-enoate, a complex organic compound, exhibits specific solubility characteristics that are vital for its applications. When discussing the solubility of this compound, various factors come into play:

  • Polarity: The presence of sodium ions contributes to the ionic nature of this compound, enhancing its solubility in polar solvents such as water.
  • Functional Groups: The presence of the bromo and methoxy groups can influence **intermolecular interactions**, impacting how well the compound dissolves.
  • Solvent Compatibility: It is typically more soluble in solvents like DMSO or ethanol due to the ability of these solvents to stabilize ionic species.
  • Temperature Dependence: Like many compounds, its solubility may increase with temperature, making it easier to dissolve in heated solvents.

To summarize, the solubility profile of sodium 3-bromo-4-(4-methoxyphenyl)-4-oxo-but-2-enoate can be described as generally favorable in polar solvents, influenced by its **chemical structure** and the nature of the solvent used. As always, practical solubility may require further empirical evaluation to determine optimal conditions for specific uses.

Interesting facts

Interesting Facts About 3-Bromo-4-(4-Methoxyphenyl)-4-Oxo-But-2-Enoate

3-Bromo-4-(4-methoxyphenyl)-4-oxo-but-2-enoate is a fascinating compound with various implications in the fields of organic chemistry and medicinal research. Here are some notable points:

  • Synthetic Utility: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those that require selective bromination and functionalization of aromatic rings.
  • Mechanism of Action: Structurally, it exhibits a unique bifunctional moiety that enables it to potentially act as both an electrophile and a nucleophile in chemical reactions, making it a versatile reagent.
  • Research Potential: Ongoing research is exploring its antitumor and antimicrobial properties, marking it as a compound to watch in drug development. Preliminary studies suggest that compounds with similar structures may inhibit cell proliferation in certain cancer types.
  • Functional Groups: The presence of both a bromine atom and a methoxy group introduces interesting electronic effects, enhancing its reactivity and potentially influencing its biological activity.
  • Canonical Forms: Researchers have discovered multiple tautomeric forms of this compound, which may lead to variations in its properties and interactions with biological targets.

In conclusion, 3-Bromo-4-(4-methoxyphenyl)-4-oxo-but-2-enoate showcases the beautiful complexity of chemical compounds. As noted by chemists, “The beauty of chemistry lies in the intricate dance of atoms and molecules, each with unique stories told through their structures.” It stands as a testament to the potential of organic synthesis in creating novel therapeutics.