Trimethyl-[[(2S,5S)-2-methyl-1,3-oxathiolan-5-yl]methyl]ammonium iodide is a quaternary ammonium compound characterized by its unique oxathiolane structure, which incorporates a sulfur atom within a five-membered ring containing oxygen. This compound features a trimethylammonium group, contributing to its cationic nature, and is typically soluble in polar solvents due to its ionic character. The presence of the iodide ion enhances its solubility and stability in various applications. The stereochemistry indicated by the (2S,5S) configuration suggests specific spatial arrangements that can influence the compound's reactivity and interactions with biological systems. Such compounds are often studied for their potential applications in pharmaceuticals, as surfactants, or in ionic liquids. Additionally, the oxathiolane moiety may impart unique properties, such as enhanced stability or specific biological activity, making it of interest in medicinal chemistry and material science. Overall, this compound exemplifies the diverse functionalities that can arise from the combination of nitrogen, sulfur, and oxygen in organic chemistry.

trimethyl-[[(2S,5S)-2-methyl-1,3-oxathiolan-5-yl]methyl]ammonium iodide

76541-57-6: Trimethyl-[[(2S,5S)-2-methyl-1,3-oxathiolan-5-yl]methyl]ammonium iodide is a quaternary ammonium compound characterized by its unique oxathiolane structure, which incorporates a sulfur atom within a five-membered ring containing oxygen. This compound features a trimethylammonium group, contributing to its cationic nature, and is typically soluble in polar solvents due to its ionic character. The presence of the iodide ion enhances its solubility and stability in various applications. The stereochemistry indicated by the (2S,5S) configuration suggests specific spatial arrangements that can influence the compound's reactivity and interactions with biological systems. Such compounds are often studied for their potential applications in pharmaceuticals, as surfactants, or in ionic liquids. Additionally, the oxathiolane moiety may impart unique properties, such as enhanced stability or specific biological activity, making it of interest in medicinal chemistry and material science. Overall, this compound exemplifies the diverse functionalities that can arise from the combination of nitrogen, sulfur, and oxygen in organic chemistry.

CAS 76541-57-6

trimethyl-[[(2S,5S)-2-methyl-1,3-oxathiolan-5-yl]methyl]ammonium iodide

cis-2-Methyl-5-trimethylammoniummethyl-1,3-oxathiolane iodide

Ref: IN-DA003OY2

cis-2-Methyl-5-trimethylammoniummethyl-1,3-oxathiolane iodide

Ref: 7W-GL9455