3-Bromo-1-hydroxy-2,2,5,5-tetramethyl-4-(methylsulfonylsulfanylmethyl)pyrrole is a complex organic compound characterized by its unique structural features, including a pyrrole ring, multiple methyl groups, and a bromine atom. The presence of the hydroxyl group contributes to its potential as a reactive intermediate in various chemical reactions. The methylsulfonylsulfanylmethyl substituent enhances its solubility in polar solvents and may influence its reactivity and biological activity. This compound is likely to exhibit interesting properties due to the steric hindrance from the tetramethyl groups, which can affect its interaction with other molecules. Additionally, the bromine atom may impart specific reactivity patterns, making it useful in synthetic organic chemistry. Its potential applications could span across pharmaceuticals, agrochemicals, or materials science, depending on its reactivity and functional properties. As with many organic compounds, safety and handling precautions should be observed due to the presence of halogens and potential biological activity.

3-bromo-1-hydroxy-2,2,5,5-tetramethyl-4-(methylsulfonylsulfanylmethyl)pyrrole

215956-55-1: 3-Bromo-1-hydroxy-2,2,5,5-tetramethyl-4-(methylsulfonylsulfanylmethyl)pyrrole is a complex organic compound characterized by its unique structural features, including a pyrrole ring, multiple methyl groups, and a bromine atom. The presence of the hydroxyl group contributes to its potential as a reactive intermediate in various chemical reactions. The methylsulfonylsulfanylmethyl substituent enhances its solubility in polar solvents and may influence its reactivity and biological activity. This compound is likely to exhibit interesting properties due to the steric hindrance from the tetramethyl groups, which can affect its interaction with other molecules. Additionally, the bromine atom may impart specific reactivity patterns, making it useful in synthetic organic chemistry. Its potential applications could span across pharmaceuticals, agrochemicals, or materials science, depending on its reactivity and functional properties. As with many organic compounds, safety and handling precautions should be observed due to the presence of halogens and potential biological activity.

<p>Applications The Bromo-analogue of MTSL, a highly reactive thiol-specific spin-label. A specific conformational probe of thiol site structure by virtue of its minimal rotational freedom and distance from the covalent disulfide linkage to the macromolecule under study.<br>References Berliner, L.J., et al.: Analytical Biochemistry, 119, 450 (1982)<br></p>

CAS 215956-55-1

3-bromo-1-hydroxy-2,2,5,5-tetramethyl-4-(methylsulfonylsulfanylmethyl)pyrrole

4-Bromo-(1-oxyl-2,2,5,5-tetramethyl-∆3-pyrroline-3-methyl) Methanethiosulfonate

Ref: TR-B686290