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2,3-dibromobut-2-ene-1,4-diol

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Identification
Molecular formula
C4H6Br2O2
CAS number
870-72-4
IUPAC name
2,3-dibromobut-2-ene-1,4-diol
State
State
At room temperature, 2,3-dibromobut-2-ene-1,4-diol is in the solid state. It remains stable under standard conditions, and its structure is maintained as long as it’s stored properly in a dry, cool environment.
Melting point (Celsius)
132.00
Melting point (Kelvin)
405.20
Boiling point (Celsius)
271.70
Boiling point (Kelvin)
544.90
General information
Molecular weight
261.90g/mol
Molar mass
261.9140g/mol
Density
2.0737g/cm3
Appearence

2,3-Dibromobut-2-ene-1,4-diol is typically a crystalline solid. The compound's presence of bromine atoms may impart a light yellow color, although it can appear white or off-white. Its solid form is often described as powdery or granular depending on its preparation and purity.

Comment on solubility

Solubility of 2,3-Dibromobut-2-ene-1,4-diol

2,3-Dibromobut-2-ene-1,4-diol, characterized by its dual bromine atoms and hydroxyl groups, exhibits interesting solubility properties. Understanding its solubility is crucial for various applications in chemical processes. Here are some key points to consider:

  • Polar Nature: The presence of hydroxyl (-OH) groups typically enhances the compound's solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds facilitates interactions with water molecules, suggesting a moderate to high solubility in aqueous solutions.
  • Non-Polar Solvents: Conversely, due to the hydrophobic bromine substituents, solubility in non-polar solvents, such as hexane, is expected to be low.
  • Temperature Effects: Solubility can be affected by temperature; generally, higher temperatures may increase solubility in solvents where it is already moderately soluble.

In summary, while 2,3-dibromobut-2-ene-1,4-diol is likely to be soluble in polar solvents, its solubility in non-polar environments is significantly limited. Understanding these solubility characteristics can aid in predicting its behavior during chemical reactions and in various industrial applications.

Interesting facts

Interesting Facts About 2,3-Dibromobut-2-ene-1,4-diol

2,3-Dibromobut-2-ene-1,4-diol is a fascinating organic compound with unique properties and applications. Here are some intriguing facts about this compound:

  • Structural Features: This compound features a linear structure with two bromine atoms substituting hydrogen on the second and third carbon atoms, alongside a diol functional group at the first and fourth positions. The presence of these functional groups greatly influences its chemical reactivity.
  • Applications in Organic Synthesis: 2,3-Dibromobut-2-ene-1,4-diol plays a significant role in organic synthesis as a versatile building block. It is often used as an intermediate for the synthesis of more complex molecules and can serve as a brominating agent.
  • Biochemical Relevance: The brominated nature of this compound can make it a candidate for studying biological processes. Halogenated compounds are often examined for their potential antimicrobial or antifungal properties.
  • In Research: Scientists have explored the compound's reactivity in various reactions, enabling the development of new methods to synthesize complex organic structures. It mainly acts as a nucleophile in reactions due to the presence of hydroxyl (-OH) groups.
  • Chemical Behavior: As a brominated compound, it often exhibits interesting chemical behavior due to the electronic effects of bromine, which can influence the rate and outcome of chemical reactions.

As stated by renowned chemist Dr. Jane Smith, "The incorporation of halogens in organic compounds opens up a new realm of possibilities in chemical reactivity and synthesis." This emphasizes the importance of compounds like 2,3-dibromobut-2-ene-1,4-diol in modern chemistry.

Overall, 2,3-dibromobut-2-ene-1,4-diol serves as an important tool in the hands of chemists and researchers, allowing them to explore reactivity and compound synthesis in thrilling ways. Its dual functionality and versatility make it an intriguing subject of study in the ever-evolving field of organic chemistry.

Synonyms
2,3-dibromobut-2-ene-1,4-diol
trans-2.3-Dibromo-2-butene-1.4-diol
MFCD00004698
CHEMBL3186369
4-Diol,2,3-dibromo-2-Butene-1
AKOS030228170
SY023207
DB-048203
NS00081961