3-(Ethyldithio)-2-methylfuran is an organic compound characterized by its unique structure, which includes a furan ring substituted with both an ethylthio group and a methyl group. The presence of the furan ring imparts aromatic properties, contributing to its potential reactivity and stability. This compound is typically a colorless to pale yellow liquid, exhibiting a distinctive odor. It is soluble in organic solvents, which makes it useful in various chemical applications, including synthesis and as an intermediate in organic chemistry. The ethylthio group enhances its nucleophilicity, making it a valuable building block in the synthesis of more complex molecules. Additionally, 3-(Ethyldithio)-2-methylfuran may exhibit biological activity, although specific studies on its pharmacological properties may be limited. As with many sulfur-containing compounds, it is important to handle it with care due to potential toxicity and reactivity. Proper safety measures should be observed when working with this substance in laboratory settings.

3-(Ethyldithio)-2-methylfuran

61197-07-7: 3-(Ethyldisulfanyl)-2-Methylfuran, Ethyl-2-methyl-3-furyl disulfide, Furan, 3-(ethyldithio)-2-methyl-, 3-(Ethyldithio)-2-methylfuran

3-(Ethyldithio)-2-methyl-fUran is an organofluorine compound that is used as a food additive. 3-(Ethyldithio)-2-methyl-fUran has been shown to be a potent inhibitor of bacterial growth and can be used to inhibit the growth of Gram positive bacteria, such as those that are resistant to antibiotics. 3-(Ethyldithio)-2-methyl-fUran inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV, which are enzymes that maintain the integrity of bacterial DNA. This binding prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division.

CAS 61197-07-7: 3-(Ethyldithio)-2-methylfuran

3-(Ethyldithio)-2-methyl-fUran

Ref: 3D-FE41570