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2,2-dibromoacetaldehyde

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Identification
Molecular formula
C2H2Br2O
CAS number
631-93-8
IUPAC name
2,2-dibromoacetaldehyde
State
State
Liquid at room temperature.
Melting point (Celsius)
-5.00
Melting point (Kelvin)
268.00
Boiling point (Celsius)
178.00
Boiling point (Kelvin)
451.00
General information
Molecular weight
215.83g/mol
Molar mass
215.8280g/mol
Density
3.0100g/cm3
Appearence
2,2-Dibromoacetaldehyde typically appears as a pale yellow to brown liquid. It may darken upon exposure to light.
Comment on solubility

Solubility of 2,2-Dibromoacetaldehyde

2,2-Dibromoacetaldehyde, with the chemical formula C2H4Br2O, exhibits interesting solubility characteristics that are influenced by its molecular structure and the presence of bromine substituents. This compound is generally soluble in a variety of organic solvents. Here are some key points regarding its solubility:

  • Solvents: 2,2-Dibromoacetaldehyde is known to dissolve well in polar solvents such as ethanol and acetone.
  • Water solubility: While it is less soluble in water compared to more polar aldehydes, it does exhibit some degree of solubility due to hydrogen bonding capabilities.
  • Influence of Bromine: The presence of bromine atoms can increase the compound’s reactivity, affecting its interaction with various solvents.

In summary, 2,2-dibromoacetaldehyde is more soluble in organic solvents than in water, making it suitable for applications in organic synthesis where organic solvents are the medium of choice. However, its solubility is not as extensive as some simpler aldehydes, illustrating the complex effects of halogenation on solubility properties.

Interesting facts

Interesting Facts about 2,2-Dibromoacetaldehyde

2,2-Dibromoacetaldehyde is a fascinating compound that belongs to the family of aldehydes. This organobromine compound has garnered attention in various fields due to its unique properties and potential applications. Here are some interesting facts:

  • Biological Activity: Researchers have investigated its biological properties, discovering that it exhibits potential antibacterial and antifungal activities, making it a candidate for medicinal chemistry applications.
  • Chemical Synthesis: The compound can be synthesized through various methods, often involving bromination reactions. Its reactivity makes it an interesting target for synthetic chemists looking to explore new pathways.
  • Applications in Research: 2,2-Dibromoacetaldehyde has been used as a reagent in the synthesis of other chemical compounds, showcasing its importance in organic chemistry.
  • Environmental Considerations: As with many organobromine compounds, it is crucial to consider the environmental impacts and toxicity associated with the use of 2,2-dibromoacetaldehyde in industrial processes.

In summary, 2,2-dibromoacetaldehyde exemplifies the intriguing nature of organic compounds. As scientists continue to delve into its properties and applications, the compound's significance in both research and industrial contexts may expand further.

Synonyms
DIBROMOACETALDEHYDE
3039-13-2
2,2-dibromoacetaldehyde
Acetaldehyde, dibromo-
Acetaldehyde, 2,2-dibromo-
dibromacetaldehyd
SCHEMBL3897423
DTXSID60184476
XIVPMNIFAAGBOY-UHFFFAOYSA-N
dibromoacetaldehyde (technical grade)
AKOS040758028
FD172168
DB-342557
HY-133647
CS-0128473
EN300-2287794