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1,2,3,5-tetrabromobenzene

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Identification
Molecular formula
C6H2Br4
CAS number
634-91-3
IUPAC name
1,2,3,5-tetrabromobenzene
State
State

At room temperature, 1,2,3,5-tetrabromobenzene is found in a solid state. The compound's high bromine content contributes to its relatively high density and crystalline structure.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
393.70g/mol
Molar mass
393.6970g/mol
Density
2.3920g/cm3
Appearence

1,2,3,5-Tetrabromobenzene is a white or off-white crystalline powder. It is characterized by its symmetrical bromine substitution pattern around the benzene ring, lending it a high degree of stability and halogenated aromatic nature.

Comment on solubility

Solubility of 1,2,3,5-Tetrabromobenzene

1,2,3,5-tetrabromobenzene (C6H2Br4) is an organic compound characterized by its extensive bromination. The solubility of this compound can be influenced by various factors, most notably its structure and the presence of bromine substituents.

Factors Affecting Solubility

  • **Polarity**: The presence of multiple bromine atoms increases the polarity of the molecule. However, due to the overall symmetry and stability of the benzene ring, it retains significant nonpolar characteristics.
  • **Solvent Interactions**: 1,2,3,5-tetrabromobenzene is more soluble in nonpolar organic solvents such as hexane and toluene. It has limited solubility in polar solvents like water.
  • **Hydrophobicity**: The brominated structure contributes to a hydrophobic nature, which decreases its solubility in aqueous environments.

Overall, the solubility profile of 1,2,3,5-tetrabromobenzene emphasizes the classic rule of solubility: "like dissolves like." Therefore, it is likely to dissolve well in nonpolar solvents while exhibiting low solubility in polar mediums such as water. This characteristic influences its applications in organic chemistry and materials science significantly.

Interesting facts

Interesting Facts about 1,2,3,5-Tetrabromobenzene

1,2,3,5-Tetrabromobenzene is a fascinating halogenated aromatic compound with numerous intriguing characteristics and applications. Here are some notable points:

  • Structure and Substitution: This compound is a derivative of benzene where four hydrogen atoms are replaced by bromine atoms at the 1st, 2nd, 3rd, and 5th positions. The presence of multiple bromine substituents significantly alters its properties compared to non-brominated benzene.
  • Applications in Chemistry: 1,2,3,5-Tetrabromobenzene is often utilized as a versatile building block in the synthesis of more complex organic molecules. Its unique reactivity is leveraged in various chemical reactions, making it a valuable compound in organic synthesis.
  • Environmental Considerations: Due to the presence of bromine, this compound may exhibit interesting environmental behavior. Some brominated compounds can be persistent in the environment, leading to vital discussions on the implications of their use in industrial settings.
  • Research Interest: Scientists are continually exploring the properties of halogenated compounds like 1,2,3,5-tetrabromobenzene in materials science and pharmacology. Their ability to act as flame retardants and potential uses in drug formulation makes them a subject of extensive research.
  • Toxicity and Safety: As with many halogenated compounds, it is crucial to handle 1,2,3,5-tetrabromobenzene with caution due to potential toxicity. Proper safety protocols must be followed when working with this compound in laboratory settings.

In summary, 1,2,3,5-tetrabromobenzene serves as an excellent example of how modified aromatic compounds can lead to new functionalities and uses in both industry and research. As we continue to explore the world of chemical compounds, understanding their properties and implications remains a critical component of scientific investigation.

Synonyms
1,2,3,5-TETRABROMOBENZENE
Benzene, 1,2,3,5-tetrabromo-
UNII-DJ06522EF4
DJ06522EF4
DTXSID8073924
DTXCID1043833
622-156-4
634-89-9
SCHEMBL6660944
AKOS024263323
G83648
Q27276419