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3,5-Dibromophenol

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Identification
Molecular formula
C6H4Br2O
CAS number
626-41-5
IUPAC name
3,5-dibromophenol
State
State

At room temperature, 3,5-Dibromophenol is typically found in a solid state, characterized by its crystalline nature.

Melting point (Celsius)
66.00
Melting point (Kelvin)
339.15
Boiling point (Celsius)
268.00
Boiling point (Kelvin)
541.15
General information
Molecular weight
265.90g/mol
Molar mass
265.9040g/mol
Density
2.2240g/cm3
Appearence

3,5-Dibromophenol appears as a white to slightly off-white crystalline solid. It is a brominated derivative of phenol and has a distinctly phenolic and slightly pungent odor.

Comment on solubility

Solubility of 3,5-dibromophenol

3,5-dibromophenol, with the chemical formula C6H4Br2O, exhibits interesting solubility properties due to its unique structure. This compound contains both bromine atoms and a hydroxyl group, which significantly influences its interaction with solvents.

Solubility Insights

When considering the solubility of 3,5-dibromophenol, it's important to note:

  • Solvent Polarities: 3,5-dibromophenol is more soluble in polar solvents such as water and ethanol due to hydrogen bonding facilitated by the -OH group.
  • Hydrophobic Character: The presence of bromine atoms adds to its hydrophobic character, making it less soluble in non-polar solvents like hexane.
  • Concentration Dependency: Solubility may be affected by concentration; at higher concentrations, the solubility might decrease due to intermolecular interactions.

Overall, while 3,5-dibromophenol can dissolve in polar solvents, care must be taken regarding the choice of solvent and the concentration of the solution. Understanding these solubility characteristics is crucial for practical applications in diverse fields.

Interesting facts

Interesting Facts about 3,5-dibromophenol

3,5-dibromophenol is a fascinating compound that occupies a significant position in the field of organic chemistry. Here are some notable aspects of this intriguing chemical:

  • Structural Importance: As a brominated phenolic compound, 3,5-dibromophenol features two bromine substituents in the meta positions of the phenol ring, which alters its reactivity and physical properties compared to unsubstituted phenol.
  • Biological Activity: Studies have shown that 3,5-dibromophenol exhibits antimicrobial properties, making it of interest for potential applications in pharmaceuticals and agriculture.
  • Applications: This compound is often utilized in the synthesis of other chemical products and as an intermediate in the production of dyes and other organic chemicals.
  • Environmental Considerations: Like many brominated compounds, 3,5-dibromophenol has raised environmental concerns due to its potential persistence and bioaccumulation. It is important to study the ecological impact of such chemicals.
  • Analytical Methods: The detection and quantification of 3,5-dibromophenol in various matrices can be performed using techniques such as gas chromatography and mass spectrometry, showcasing its role in analytical chemistry.

Beyond its chemical properties, 3,5-dibromophenol serves as a reminder of the intricate relationships between structure and function in organic molecules. As Linus Pauling once said, "The best way to have a good idea is to have lots of ideas," and compounds like 3,5-dibromophenol inspire further exploration of chemical interactions and applications.

In conclusion, 3,5-dibromophenol is not just a simple chemical; it represents the vast potential of organic chemistry to impact various fields, from medicine to environmental science.

Synonyms
3,5-DIBROMOPHENOL
Phenol, 3,5-dibromo-
DTXSID70211646
DTXCID00134137
629-188-8
626-41-5
3,5-Dibromphenol
MFCD06411376
3,5-Dibromo-phenol
3, 5-dibromophenol
3-,5-dibromophenol
3,5-Dibromophenol, 97%
SCHEMBL309955
CHEMBL450082
BCP05888
TD1260
AKOS005068134
CS-W007905
GS-3389
HY-W007905
AC-28709
SY012996
DB-002493
D3820
EN300-113704
Q223012