2-(Naphthalen-1-yl)-1H-benzimidazole, with the CAS number 2562-81-4, is an organic compound characterized by its fused aromatic ring structure, which includes a naphthalene moiety and a benzimidazole unit. This compound typically exhibits properties associated with both aromatic systems, such as stability and potential for π-π stacking interactions. It is generally insoluble in water but may dissolve in organic solvents, reflecting its hydrophobic nature. The presence of nitrogen in the benzimidazole ring contributes to its basicity and potential for forming hydrogen bonds, which can influence its reactivity and interactions with other molecules. This compound may be of interest in various fields, including organic electronics, pharmaceuticals, and materials science, due to its electronic properties and potential biological activity. Its synthesis often involves multi-step organic reactions, and it may serve as a precursor or building block for more complex chemical entities. Overall, 2-(naphthalen-1-yl)-1H-benzimidazole is a versatile compound with significant implications in research and application.

2-(naphthalen-1-yl)-1H-benzimidazole

2562-81-4: 2-(Naphthalen-1-yl)-1H-benzimidazole, with the CAS number 2562-81-4, is an organic compound characterized by its fused aromatic ring structure, which includes a naphthalene moiety and a benzimidazole unit. This compound typically exhibits properties associated with both aromatic systems, such as stability and potential for π-π stacking interactions. It is generally insoluble in water but may dissolve in organic solvents, reflecting its hydrophobic nature. The presence of nitrogen in the benzimidazole ring contributes to its basicity and potential for forming hydrogen bonds, which can influence its reactivity and interactions with other molecules. This compound may be of interest in various fields, including organic electronics, pharmaceuticals, and materials science, due to its electronic properties and potential biological activity. Its synthesis often involves multi-step organic reactions, and it may serve as a precursor or building block for more complex chemical entities. Overall, 2-(naphthalen-1-yl)-1H-benzimidazole is a versatile compound with significant implications in research and application.

CAS 2562-81-4

2-(naphthalen-1-yl)-1H-benzimidazole

2-(Naphthalen-1-yl)-1H-1,3-benzodiazole

Ref: 3D-CAA56281