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
Molecular Weight
314.79g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
2.0600g/cm3
Synonyms
SCHEMBL368221
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.
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