2-[(4-Chlorobenzyl)sulfanyl]aniline, with the CAS number 43092-84-8, is an organic compound characterized by the presence of both an aniline and a thioether functional group. This compound features a benzyl group substituted with a chlorine atom at the para position relative to the sulfur atom, which is linked to the aniline moiety. The presence of the sulfur atom introduces unique chemical properties, such as potential reactivity in nucleophilic substitution reactions and the ability to form various derivatives. The compound is likely to exhibit moderate solubility in organic solvents due to its hydrophobic aromatic components, while its aniline structure may impart some degree of basicity. Additionally, the chlorobenzyl group can influence the compound's electronic properties, potentially affecting its reactivity and interactions with biological systems. Overall, 2-[(4-chlorobenzyl)sulfanyl]aniline is of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in drug development and as a building block for more complex molecules.

2-[(4-chlorobenzyl)sulfanyl]aniline

43092-84-8: 2-[(4-Chlorobenzyl)sulfanyl]aniline, with the CAS number 43092-84-8, is an organic compound characterized by the presence of both an aniline and a thioether functional group. This compound features a benzyl group substituted with a chlorine atom at the para position relative to the sulfur atom, which is linked to the aniline moiety. The presence of the sulfur atom introduces unique chemical properties, such as potential reactivity in nucleophilic substitution reactions and the ability to form various derivatives. The compound is likely to exhibit moderate solubility in organic solvents due to its hydrophobic aromatic components, while its aniline structure may impart some degree of basicity. Additionally, the chlorobenzyl group can influence the compound's electronic properties, potentially affecting its reactivity and interactions with biological systems. Overall, 2-[(4-chlorobenzyl)sulfanyl]aniline is of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in drug development and as a building block for more complex molecules.

CAS 43092-84-8

2-[(4-chlorobenzyl)sulfanyl]aniline

2-[(4-chlorobenzyl)thio]aniline

Ref: 10-F314592