4,6-Difluoro-2-(trifluoromethyl)-1H-benzimidazole is a chemical compound characterized by its unique structure, which includes a benzimidazole core substituted with fluorine atoms. The presence of two fluorine atoms at the 4 and 6 positions, along with a trifluoromethyl group at the 2 position, contributes to its distinct chemical properties. This compound is typically a solid at room temperature and exhibits high stability due to the strong C-F bonds. Its fluorinated nature often imparts increased lipophilicity and potential bioactivity, making it of interest in pharmaceutical and agrochemical research. The compound may exhibit specific reactivity patterns, including nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing effects of the fluorine substituents. Additionally, its solubility characteristics can vary based on the solvent used, and it may show interesting interactions in biological systems, which could be explored for various applications. Overall, 4,6-difluoro-2-(trifluoromethyl)-1H-benzimidazole is a notable compound in the field of synthetic chemistry and drug development.

4,6-difluoro-2-(trifluoromethyl)-1H-benzimidazole

89426-93-7: 4,6-Difluoro-2-(trifluoromethyl)-1H-benzimidazole is a chemical compound characterized by its unique structure, which includes a benzimidazole core substituted with fluorine atoms. The presence of two fluorine atoms at the 4 and 6 positions, along with a trifluoromethyl group at the 2 position, contributes to its distinct chemical properties. This compound is typically a solid at room temperature and exhibits high stability due to the strong C-F bonds. Its fluorinated nature often imparts increased lipophilicity and potential bioactivity, making it of interest in pharmaceutical and agrochemical research. The compound may exhibit specific reactivity patterns, including nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing effects of the fluorine substituents. Additionally, its solubility characteristics can vary based on the solvent used, and it may show interesting interactions in biological systems, which could be explored for various applications. Overall, 4,6-difluoro-2-(trifluoromethyl)-1H-benzimidazole is a notable compound in the field of synthetic chemistry and drug development.

4,6-Difluoro-2-(trifluoromethyl)-1H-benzimidazole

CAS 89426-93-7

4,6-difluoro-2-(trifluoromethyl)-1H-benzimidazole

4,6-Difluoro-2-(trifluoromethyl)-1H-benzimidazole

Ref: 54-PC502055

4,6-Difluoro-2-(trifluoromethyl)-1H-benzo[d]imidazole

Ref: 10-F778983