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Dibromoquinone

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Identification
Molecular formula
C14H8Br2O4
CAS number
1105-24-0
IUPAC name
1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione
State
State

At room temperature, dibromoquinone is a solid.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.00
Boiling point (Celsius)
395.00
Boiling point (Kelvin)
668.00
General information
Molecular weight
381.99g/mol
Molar mass
381.9940g/mol
Density
2.3400g/cm3
Appearence

Dibromoquinone is a yellow to light-brown crystalline solid.

Comment on solubility

Solubility of 1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione

The solubility of 1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione can be quite intricate due to its unique molecular structure and functional groups. A few key points regarding its solubility are as follows:

  • Polarity: The presence of bromine and hydroxyl groups contributes to its overall polarity, which can affect its interactions with solvents.
  • Solvent Compatibility: This compound may exhibit good solubility in organic solvents such as:
    • Dimethyl sulfoxide (DMSO)
    • Ethyl acetate
    • Acetone
  • Water Solubility: Due to its organic functional groups, 1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione may have limited solubility in water.

As with many complex organic compounds, it’s essential to consider environmental conditions and ionic interactions, as they can significantly influence solubility behavior. Always refer to empirical data for precise information and conduct solubility tests to confirm theoretical predictions.

Interesting facts

Interesting Facts about 1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione

This compound is a notable example of an organobromine compound, showcasing the intricate relationship between halogen chemistry and the biological activity of various organic molecules. Here are some interesting insights:

  • 1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione contains both bromine and hydroxyl functional groups, which significantly contribute to its chemical reactivity and potential biological applications.
  • The presence of bromine makes this compound of interest in medicinal chemistry, as brominated compounds can show enhanced therapeutic effects compared to their non-brominated counterparts.
  • This compound belongs to a class known for their **antioxidant** properties, potentially acting as a scavenger of free radicals in biological systems, which is vital for preventing cellular damage.

Applications in Research

Researchers have been investigating compounds like 1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione for their potential roles in:

  • Pharmaceutical Development: The structure may serve as a starting point for the design of new drugs with better efficacy and safety.
  • Organic Synthesis: Due to its unique functional groups, it could be utilized as an intermediate in the synthesis of more complex organic molecules.
  • Biological Studies: Its properties may provide insight into the molecular mechanisms underlying oxidative stress in cells.

Overall, the study of 1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione not only enriches our understanding of organic chemistry but also opens avenues toward innovative applications in medicine and material science. As scientists continue to explore such compounds, they often say, “The key to unlocking new discoveries lies in the unexpected behavior of molecules.”

Synonyms
Dibromsalicil
Dibromosalicil
523-88-6
5,5'-Dibromosalicil
Dibromosalicyl
Degermon
Dibrosal
Dibrosil
Respectol
Bis(5-bromo-2-hydroxyphenyl)ethanedione
1,2-bis(5-bromo-2-hydroxyphenyl)ethane-1,2-dione
Z2V3FF4B7F
MLS002638309
Ethanedione, bis(5-bromo-2-hydroxyphenyl)-
NSC-13235
Fungotox (VAN)
EINECS 208-351-3
NSC 13235
5,5'-Dibromo-2,2'-dihydroxybenzil
UNII-Z2V3FF4B7F
Salicil, 5,5'-dibromo-
5,5'-Dibromo-2,2'-dihydroxybibenzoyl
BRN 3384611
Fungotox
5,5'-Dibrom-2,2'-dioxybenzil [German]
5,5'-Dibrom-2,2'-dioxybenzil
5,2'-dioxybenzil
Salicil,5'-dibromo-
5,2'-dihydroxybenzil
5,2'-dihydroxybibenzoyl
DIBROMSALICIL [MI]
Benzil-based compound, 31
cid_10662
CHEMBL366205
SCHEMBL2156880
WLN: QR DE BVVR BQ EE
BDBM22753
DTXSID20200328
AAOYLOCWJSLLJU-UHFFFAOYSA-N
HMS3086D19
NSC13235
AKOS027382229
Bis-(5-brom-2-hydroxyphenyl)ethandion
PD129618
SMR001547796
NS00032499
1,2-bis(5-bromo-2-hydroxyphenyl)-1,2-ethanedione
1,2-bis(5-bromo-2-hydroxy-phenyl)ethane-1,2-dione
Q27294920