4-bromo-6-nitro-2-(trifluoromethyl)-1H-benzimidazole

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Identification

Molecular formula
C8H3BrF3N3O2
CAS Number
141920-92-9
IUPAC Name
4-bromo-6-nitro-2-(trifluoromethyl)-1H-benzimidazole
Molecular Weight
312.00g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.8000g/cm3
Synonyms
BENZIMIDAZOLE, 4-BROMO-6-NITRO-2-(TRIFLUOROMETHYL)-
Interesting facts

Interesting Facts about 4-bromo-6-nitro-2-(trifluoromethyl)-1H-benzimidazole

4-bromo-6-nitro-2-(trifluoromethyl)-1H-benzimidazole is a fascinating compound that integrates the properties of both halogens and nitro groups in its molecular structure. This compound is a derivative of benzimidazole, a class of compounds that has gained attention for their numerous biological activities.

Key Features

  • Pharmacological Potential: Compounds related to benzimidazole often exhibit a range of biological activities, including anti-inflammatory, anti-cancer, and anti-viral effects. The presence of both bromine and nitro substitutions could further enhance these biological properties.
  • Electrophilic Nature: The trifluoromethyl group is known for making compounds more electrophilic, influencing the reactivity of 4-bromo-6-nitro-2-(trifluoromethyl)-1H-benzimidazole in various chemical reactions.
  • Versatile Building Block: This compound serves as an important synthetic precursor in organic chemistry, allowing for the construction of more complex molecules through various reactions such as nucleophilic substitution.

In the scientific community, compounds like 4-bromo-6-nitro-2-(trifluoromethyl)-1H-benzimidazole are often explored for their potential applications in medicinal chemistry. As research continues, we may uncover even more exciting uses for this compound.

Quote from a Research Chemist: "Understanding the intricacies of compound substitutions not only allows us to predict reactivity but also opens the door to synthesizing new therapeutic agents."

In summary, the unique structure of 4-bromo-6-nitro-2-(trifluoromethyl)-1H-benzimidazole presents numerous opportunities for scientific exploration, enabling chemists to venture into new medicinal territories and uncover novel applications.

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