Interesting facts
Interesting Facts About 1,2,3,4-Tetrabromobenzene
1,2,3,4-Tetrabromobenzene is a fascinating compound that plays a significant role in various chemical reactions and applications. Here are some interesting aspects of this aromatic compound:
- Halogenated Aromatic Compound: 1,2,3,4-tetrabromobenzene contains four bromine atoms attached to a benzene ring, making it a member of the halogenated aromatic compounds.
- Environmental Impact: Due to its bromine content, this compound has been studied for its environmental effects, as brominated compounds can accumulate in living organisms and the environment.
- Applications: It serves as a versatile building block in organic synthesis, especially in creating other complex molecules, polymers, and materials. Chemists often utilize it in synthetic pathways to introduce bromine functionality.
- Research Interest: The study of 1,2,3,4-tetrabromobenzene is prevalent in material science and medicinal chemistry, where researchers explore its properties and potential therapeutic applications.
- Unique Reactivity: The presence of multiple bromine substituents affects the reactivity of the compound, making it a useful compound in electrophilic substitution reactions.
It's exciting to see how compounds like 1,2,3,4-tetrabromobenzene contribute to advancing our understanding of chemistry and its myriad applications. As we continue to explore their properties, researchers remain focused on potential innovations they may offer in various fields.
Synonyms
1,2,3,4-TETRABROMOBENZENE
Benzene, 1,2,3,4-tetrabromo-
UNII-LV347866P3
LV347866P3
DTXSID8074021
RefChem:196665
DTXCID7036662
22311-25-7
tetrabromobenzene
SCHEMBL149175
SCHEMBL358557
SCHEMBL4375071
SCHEMBL29646281
MFCD18399967
SY272435
Q27283198
Solubility of 1,2,3,4-Tetrabromobenzene
1,2,3,4-Tetrabromobenzene, with the chemical formula C6H2Br4, exhibits interesting solubility characteristics due to its complex structure. Here are some key points to consider:
In summary, 1,2,3,4-tetrabromobenzene highlights the general principle that halogenated aromatic compounds often exhibit low solubility in polar solvents such as water. Conversely, they prefer non-polar solvents, emphasizing the role of molecular structure in determining solubility behaviors.