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3-(4-bromophenyl)-3-chloroprop-2-enal

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Identification
Molecular formula
C9H6BrClO
CAS number
60712-54-5
IUPAC name
3-(4-bromophenyl)-3-chloro-prop-2-enal
State
State

At room temperature, 3-(4-bromophenyl)-3-chloroprop-2-enal is generally a solid, especially in a purified form. It can sublimate and emit odors characteristic of its aldehyde group at elevated temperatures.

Melting point (Celsius)
59.00
Melting point (Kelvin)
332.15
Boiling point (Celsius)
328.00
Boiling point (Kelvin)
601.15
General information
Molecular weight
247.49g/mol
Molar mass
247.4870g/mol
Density
1.5936g/cm3
Appearence

3-(4-bromophenyl)-3-chloroprop-2-enal typically appears as a pale yellow crystalline solid. It can be characterized by its distinct acrolein-like smell, common to aldehydes with aromatic and halogenated groups.

Comment on solubility

Solubility of 3-(4-bromophenyl)-3-chloro-prop-2-enal

The solubility of 3-(4-bromophenyl)-3-chloro-prop-2-enal is an intriguing subject, particularly due to its structural attributes and the presence of halogen substituents. Here are key points to consider:

  • Solvent Dependency: This compound is expected to exhibit variable solubility profiles depending on the solvent used. For example, it may be more soluble in organic solvents like ethanol or acetone than in water due to its hydrophobic character.
  • Halogen Effects: The presence of Br (bromine) and Cl (chlorine) atoms can influence solubility by impacting intermolecular interactions. Halogens often contribute to increased molecular weight, which can reduce solubility in polar solvents.
  • Temperature Influence: Like many organic compounds, the solubility of 3-(4-bromophenyl)-3-chloro-prop-2-enal may increase with temperature. Heating can disrupt solute-solvent interactions, enhancing dissolution.

Overall, this compound demonstrates that solubility is not just a simple property but a complex interplay of molecular interactions. It can be said that, in organic chemistry, "like dissolves like," meaning non-polar solvents will be more effective in dissolving this compound due to its non-polar characteristics.

Interesting facts

Interesting Facts about 3-(4-Bromophenyl)-3-Chloro-Prop-2-Enal

This compound, with its intriguing structure, is a notable member of the class of alpha, beta-unsaturated aldehydes. Its unique composition leads to a variety of compelling chemical properties and potential applications:

  • Reactivity: The presence of the electron-withdrawing chloro and bromo substituents enhances the reactivity of the molecule, making it an excellent candidate for nucleophilic addition reactions.
  • Potential Applications: Due to its structure, this compound can serve as a synthetic intermediate in the production of a range of biologically active molecules and pharmaceuticals.
  • Fluorescent Properties: When incorporated into materials, compounds like this may exhibit interesting photophysical properties, making them suitable for studies in materials science and photonics.
  • Significance in Research: As an intermediary in organic synthesis, it finds diverse applications in the development of functional materials and agrochemicals, drawing the attention of chemists globally.

In the words of a noted chemist, “The beauty of organic chemistry lies in the versatility of compounds like 3-(4-bromophenyl)-3-chloro-prop-2-enal, which open doors to innovative reactions and applications.”

This compound is not merely a collection of atoms; it represents a myriad of possibilities in research and industrial applications, making it a significant topic of study for both chemists and students alike.

Synonyms
DTXSID301285519
3-(4-Bromophenyl)-3-chloro-2-propenal
DTXCID301716203
3-(4-bromophenyl)-3-chloropropenal
3-(4-BROMOPHENYL)-3-CHLOROPROP-2-ENAL
SCHEMBL2559234