Ethyl 2-(trifluoromethyl)-1H-benzimidazole-6-carboxylate is a chemical compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. The presence of a trifluoromethyl group (-CF3) at the 2-position enhances its lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry. The ethyl ester functional group contributes to its solubility and reactivity, allowing for potential applications in organic synthesis and pharmaceutical development. This compound may exhibit various properties, including specific melting and boiling points, solubility in organic solvents, and stability under certain conditions. Its unique structure suggests potential uses in agrochemicals or as a building block in the synthesis of more complex molecules. As with many fluorinated compounds, it may also exhibit distinct electronic properties due to the electronegative fluorine atoms, which can affect its interactions with biological targets. Safety and handling precautions should be observed, as with all chemical substances, particularly those with fluorinated groups.

ethyl 2-(trifluoromethyl)-1H-benzimidazole-6-carboxylate

89457-09-0: Ethyl 2-(trifluoromethyl)-1H-benzimidazole-6-carboxylate is a chemical compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. The presence of a trifluoromethyl group (-CF3) at the 2-position enhances its lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry. The ethyl ester functional group contributes to its solubility and reactivity, allowing for potential applications in organic synthesis and pharmaceutical development. This compound may exhibit various properties, including specific melting and boiling points, solubility in organic solvents, and stability under certain conditions. Its unique structure suggests potential uses in agrochemicals or as a building block in the synthesis of more complex molecules. As with many fluorinated compounds, it may also exhibit distinct electronic properties due to the electronegative fluorine atoms, which can affect its interactions with biological targets. Safety and handling precautions should be observed, as with all chemical substances, particularly those with fluorinated groups.

<p>Ethyl 2-(trifluoromethyl)-1H-1,3-benzodiazole-5-carboxylate</p>

CAS 89457-09-0

ethyl 2-(trifluoromethyl)-1H-benzimidazole-6-carboxylate

Ethyl 2-(trifluoromethyl)-1H-1,3-benzodiazole-5-carboxylate

Ref: 54-PC200376