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1,3,5-tribromobenzene

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Identification
Molecular formula
C6H3Br3
CAS number
626-39-1
IUPAC name
1,2,3-tribromobenzene;1,2,4-tribromobenzene;1,3,5-tribromobenzene
State
State

At room temperature, 1,3,5-Tribromobenzene is in a solid state.

Melting point (Celsius)
86.00
Melting point (Kelvin)
359.15
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
314.79g/mol
Molar mass
314.8280g/mol
Density
2.0600g/cm3
Appearence

1,3,5-Tribromobenzene is a white to off-white crystalline solid. It is usually found in purity suitable for laboratory and industrial applications.

Comment on solubility

Solubility of Tribromobenzenes

The solubility of tribromobenzene compounds varies significantly depending on their specific structural arrangement. Here’s a look at the solubility characteristics of:

  • 1,2,3-Tribromobenzene: This compound typically exhibits low solubility in water due to its hydrophobic nature. However, it is more soluble in organic solvents like ethanol and acetone.
  • 1,2,4-Tribromobenzene: Similar to its isomers, this variant displays low aqueous solubility. It is also better suited for solubilization in non-polar solvents, reflecting its non-polar characteristics.
  • 1,3,5-Tribromobenzene: Like the others, this compound is practically insoluble in water yet shows a good affinity for organic solvents, indicating its reliance on non-polar environments for solvation.

In general, **the tribromobenzenes can be summarized by the following characteristics**:

  • All three isomers are insoluble in water.
  • They demonstrate greater solubility in various organic solvents.
  • The substitution pattern of bromine atoms affects their physical properties but not significantly their solubility.

In summary, tribromobenzenes, with their distinct branched bromine arrangements, make a captivating study in solubility characteristics. As a class, they underscore the fundamental principle that the non-polar nature often dictates solubility behaviors, particularly in organic solvents, reinforcing the old adage: "Like dissolves like."

Interesting facts

Interesting Facts about 1,2,3-Tribromobenzene

1,2,3-Tribromobenzene is one of the isomeric forms of tribromobenzene, distinguished by its specific arrangement of bromine atoms on the benzene ring. Here are some intriguing points about this compound:

  • Isomeric Diversity: This compound is part of a larger group of tribromobenzenes, each varying in the positioning of bromine substituents. Its unique isomer configuration impacts its reactivity and applications.
  • Applications: 1,2,3-Tribromobenzene is utilized in organic synthesis, serving as an effective building block in the creation of more complex organic molecules.
  • Adverse Effects: Like many brominated compounds, it can pose environmental hazards, given that brominated hydrocarbons are known to have persistent effects on aquatic ecosystems.

Interesting Facts about 1,2,4-Tribromobenzene

This isomer of tribromobenzene features bromine atoms at the 1, 2, and 4 positions on the benzene ring. Here are some noteworthy aspects:

  • Utilization in Research: 1,2,4-Tribromobenzene is often mentioned in studies related to halogenated organic compounds, especially concerning their behavior in biological systems.
  • Spectroscopic Studies: This compound exhibits unique spectroscopic characteristics that make it interesting for researchers trying to explore interactions at the molecular level.
  • Challenging Chemistry: The substitution pattern influences reactivity in nucleophilic aromatic substitution reactions, which are pivotal in organic synthesis.

Interesting Facts about 1,3,5-Tribromobenzene

1,3,5-Tribromobenzene represents another unique isomer of tribromobenzene. It is known for several interesting properties:

  • Symmetrical Structure: Its symmetrical arrangement allows it to have distinctive physical and chemical properties compared to its ortho and para counterparts.
  • Role in Material Science: This compound has application potential in the field of material science, especially in the development of polymers and other advanced materials.
  • Toxicology Studies: As with other brominated compounds, it is frequently studied for its toxicity and environmental impact, particularly in the context of bioaccumulation and long-term ecological effects.
Synonyms
SCHEMBL368221