2-(1H-benzimidazol-2-yl)ethanethiol, with the CAS number 2242-96-8, is an organic compound characterized by the presence of a benzimidazole moiety and a thiol functional group. This compound typically appears as a solid or liquid, depending on its purity and specific conditions. It features a sulfur atom bonded to a two-carbon ethyl chain, which is further connected to a benzimidazole ring, a bicyclic structure known for its aromatic properties and nitrogen heteroatoms. The thiol group (-SH) imparts notable reactivity, allowing for potential applications in various chemical reactions, including nucleophilic substitutions and the formation of disulfides. Additionally, the benzimidazole component contributes to its biological activity, making it of interest in medicinal chemistry for potential therapeutic applications. The compound is generally soluble in polar solvents, and its properties can be influenced by factors such as pH and the presence of other functional groups. Safety data should be consulted for handling, as thiols can be malodorous and may pose health risks.

2-(1H-benzimidazol-2-yl)ethanethiol

2242-96-8: 1H-benzimidazole-2-ethanethiol,  2-(1H-Benzimidazol-2-yl)ethanethiol

2-(1H-Benzimidazol-2-yl)ethanethiol is a thioether that has been shown to exhibit anion activity. It can be synthesized by reacting 2-(1H-benzimidazol-2-yl)acetic acid with ethanethiol in the presence of copper, followed by hydrolysis. The compound displays potentials that range from -0.8 V to -0.9 V depending on the nature of the substituents and solvent. 2-(1H-Benzimidazol-2-yl)ethanethiol has also been shown to have spectra that are unsymmetrical and rhombic, which is due to its electronic properties. This compound is able to form crystal structures with chloride ions at potentials as high as 1.5 V, which are geometries that are not found for other thioethers.

CAS 2242-96-8: 2-(1H-benzimidazol-2-yl)ethanethiol

2-(1H-benzimidazol-2-yl)ethanethiol

Ref: 10-F496329

2-(1H-Benzimidazol-2-yl)ethanethiol

Ref: 3D-CAA24296