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CAS 89457-10-3

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5-Bromo-7-chloro-2-(trifluoromethyl)-1H-benzimidazole

Description:
5-Bromo-7-chloro-2-(trifluoromethyl)-1H-benzimidazole is a heterocyclic organic compound characterized by its fused benzene and imidazole rings. The presence of bromine and chlorine substituents, along with a trifluoromethyl group, contributes to its unique chemical properties and reactivity. This compound typically exhibits moderate to high lipophilicity due to the halogen substituents, which can influence its solubility in organic solvents. The trifluoromethyl group is known for enhancing biological activity and stability, making this compound of interest in pharmaceutical research. Additionally, the halogen atoms can participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of antimicrobial or anticancer agents. Its specific interactions with biological targets would depend on the overall molecular conformation and electronic distribution influenced by the halogen substituents. As with many halogenated compounds, safety and environmental considerations are essential when handling and using this substance in research and industrial applications.
Formula:C8H3BrClF3N2
InChI:InChI=1S/C8H3BrClF3N2/c9-3-1-4(10)6-5(2-3)14-7(15-6)8(11,12)13/h1-2H,(H,14,15)
InChI key:InChIKey=GQUMVBCXDLOULU-UHFFFAOYSA-N
SMILES:ClC1=C2C(N=C(C(F)(F)F)N2)=CC(Br)=C1
Synonyms:
  • 1H-Benzimidazole, 6-bromo-4-chloro-2-(trifluoromethyl)-
  • 5-Bromo-7-chloro-2-(trifluoromethyl)-1H-benzimidazole
  • 1H-Benzimidazole, 5-bromo-7-chloro-2-(trifluoromethyl)-
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