1H-Benzimidazole, 2-(2-thienyl)-, with the CAS number 3878-18-0, is an organic compound characterized by its fused benzimidazole and thienyl structures. This compound features a benzimidazole core, which consists of a benzene ring fused to an imidazole ring, providing it with notable aromatic properties and potential biological activity. The presence of the thienyl group, derived from thiophene, introduces sulfur into the molecular structure, which can influence the compound's reactivity and solubility. Typically, compounds of this nature exhibit interesting pharmacological properties, making them subjects of research in medicinal chemistry. They may also demonstrate fluorescence and have applications in organic electronics or as intermediates in the synthesis of more complex molecules. The compound's stability, solubility in various solvents, and reactivity with other chemical species can vary based on its specific molecular interactions and the presence of functional groups. Overall, 1H-Benzimidazole, 2-(2-thienyl)- is a versatile compound with potential applications in various fields of chemistry and materials science.

1H-Benzimidazole, 2-(2-thienyl)-

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2-(2-Thienyl)-1H-benzimidazole is an antibacterial that has been shown to have a broad spectrum of activity against Gram-positive bacteria. It is a metal cation chelator and forms a tautomeric form with chloride. 2-(2-Thienyl)-1H-benzimidazole has been shown to be effective against Leishmania and inhibits the synthesis of DNA, RNA, and protein in bacteria. This drug also binds to the target site on the enzyme DNA gyrase, which prevents the formation of supercoils in DNA and thereby inhibits bacterial growth.

CAS 3878-18-0: 1H-Benzimidazole, 2-(2-thienyl)-

2-(2-Thienyl)-1H-benzimidazole

Ref: 3D-DAA87818

2-(Thiophen-2-Yl)-1H-Benzo[d]Imidazole

Ref: 54-OR1027679

2-(2-Thienyl)-1H-benzimidazole

Ref: 10-F098024