2-(Phenylsulfinyl)ethanamine, identified by its CAS number 60523-52-6, is an organic compound characterized by the presence of both an amine and a sulfinyl functional group. This compound features a two-carbon ethyl chain attached to a phenylsulfinyl group, which contributes to its unique chemical properties. The sulfinyl group (–S(=O)–) enhances the compound's reactivity and polarity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The amine functional group (–NH2) imparts basicity and can participate in hydrogen bonding, influencing its solubility in polar solvents. Additionally, the presence of the phenyl ring can provide stability and influence the compound's electronic properties. Due to these characteristics, 2-(phenylsulfinyl)ethanamine may have applications in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals or as an intermediate in chemical reactions. Its specific reactivity and interactions would depend on the surrounding conditions and the presence of other functional groups in a given reaction context.

2-(phenylsulfinyl)ethanamine

60523-52-6: 2-(Phenylsulfinyl)ethanamine, identified by its CAS number 60523-52-6, is an organic compound characterized by the presence of both an amine and a sulfinyl functional group. This compound features a two-carbon ethyl chain attached to a phenylsulfinyl group, which contributes to its unique chemical properties. The sulfinyl group (–S(=O)–) enhances the compound's reactivity and polarity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The amine functional group (–NH2) imparts basicity and can participate in hydrogen bonding, influencing its solubility in polar solvents. Additionally, the presence of the phenyl ring can provide stability and influence the compound's electronic properties. Due to these characteristics, 2-(phenylsulfinyl)ethanamine may have applications in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals or as an intermediate in chemical reactions. Its specific reactivity and interactions would depend on the surrounding conditions and the presence of other functional groups in a given reaction context.

CAS 60523-52-6

2-(phenylsulfinyl)ethanamine

2-(Benzenesulfinyl)ethan-1-amine hydrochloride

Ref: 3D-KCA52352