Skip to main content

2,3-Dibromophenol

ADVERTISEMENT
Identification
Molecular formula
C6H4Br2O
CAS number
612-83-9
IUPAC name
2,3-dibromophenol
State
State

At room temperature, 2,3-dibromophenol is in a solid state. It is typically found in its crystalline form.

Melting point (Celsius)
53.00
Melting point (Kelvin)
326.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
251.90g/mol
Molar mass
251.9030g/mol
Density
2.2200g/cm3
Appearence

2,3-Dibromophenol is a white to off-white crystalline solid. It may appear slightly yellow due to impurities. It is often encountered as a powder or fine crystalline material.

Comment on solubility

Solubility of 2,3-dibromophenol

2,3-dibromophenol (C6H4Br2O) is known for its unique solubility characteristics. Its solubility can be described as follows:

  • Water Solubility: 2,3-dibromophenol exhibits limited solubility in water. This is primarily due to the presence of the bulky bromine atoms, which interfere with the ability of the molecules to engage in hydrogen bonding with water.
  • Solubility in Organic Solvents: It is notably more soluble in organic solvents, such as:
    • Alcohols
    • Aromatics
    • Chloroform
  • Temperature Dependency: The solubility can also be influenced by temperature. Generally, increased temperature leads to increased solubility in organic solvents, which is a common trend in many organic compounds.

Overall, understanding the solubility profile of 2,3-dibromophenol is crucial for its applications in various chemical processes, as it determines how this compound interacts in different environments.

Interesting facts

Interesting Facts about 2,3-Dibromophenol

2,3-Dibromophenol is a fascinating compound that plays a crucial role in various chemical applications. Here are some intriguing aspects of this compound:

  • Structural Significance: The 2 and 3 positions on the benzene ring are substituted with bromine atoms, making it a member of the bromophenol family, which are recognized for their diverse chemical properties.
  • Reactivity: 2,3-Dibromophenol is known for its activity as a precursor in the synthesis of other brominated compounds, demonstrating its versatility in organic synthesis.
  • Applications: This compound serves as a reagent in various chemical reactions, including the synthesis of dyes and pharmaceuticals. Its bromine substituents enhance its reactivity, making it a valuable intermediate in synthetic pathways.
  • Biological Impact: Interestingly, some studies have suggested that bromophenol derivatives can exhibit antimicrobial properties, paving the way for potential applications in medicine and agriculture.
  • Toxicity Consideration: While it has useful applications, safety is paramount. The compound must be handled with care, as brominated compounds can pose hazards to health and the environment.

In Summary

2,3-Dibromophenol is more than just a simple organic compound. Its unique structure and multifunctionality highlight its significance in the realm of chemistry. Regularly investigated in the laboratory, it exemplifies the balance of utility and caution in chemical research. As one researcher put it, “The exploration of compounds like 2,3-dibromophenol not only enriches our understanding of chemistry but also showcases the intricate dance of reactivity and structure.”

Synonyms
2,3-DIBROMOPHENOL
57383-80-9
DTXSID501334116
RefChem:1059326
DTXCID101379332
DIBROMOPHENOL
MFCD08166474
28514-45-6
dibromo-phenol
2,3-Dibromophenol, 95%
SCHEMBL386016
SCHEMBL1043235
SCHEMBL9732644
SCHEMBL9732647
FNAKEOXYWBWIRT-UHFFFAOYSA-N
AKOS024168482
MB05354
AS-33033
SY242055
CS-0111263
F459192
Q209166