1-(4-Chlorophenyl)-2-mercaptoethanone, with the CAS number 23081-12-1, is an organic compound characterized by the presence of a chlorophenyl group and a thiol functional group. This compound features a ketone functional group adjacent to a thiol (-SH) group, which contributes to its reactivity and potential applications in organic synthesis. The chlorophenyl moiety enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The presence of the mercapto group allows for potential interactions with various biological targets, including enzymes and receptors. This compound may exhibit properties such as antimicrobial or antifungal activity, although specific biological effects would depend on the context of its use. Additionally, its chemical structure suggests it may participate in nucleophilic substitution reactions due to the thiol group, making it a versatile intermediate in synthetic organic chemistry. Safety data should be consulted for handling and usage, as compounds containing thiols can be sensitive to oxidation and may have specific toxicity profiles.

1-(4-chlorophenyl)-2-mercaptoethanone

23081-12-1: 1-(4-Chlorophenyl)-2-mercaptoethanone, with the CAS number 23081-12-1, is an organic compound characterized by the presence of a chlorophenyl group and a thiol functional group. This compound features a ketone functional group adjacent to a thiol (-SH) group, which contributes to its reactivity and potential applications in organic synthesis. The chlorophenyl moiety enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The presence of the mercapto group allows for potential interactions with various biological targets, including enzymes and receptors. This compound may exhibit properties such as antimicrobial or antifungal activity, although specific biological effects would depend on the context of its use. Additionally, its chemical structure suggests it may participate in nucleophilic substitution reactions due to the thiol group, making it a versatile intermediate in synthetic organic chemistry. Safety data should be consulted for handling and usage, as compounds containing thiols can be sensitive to oxidation and may have specific toxicity profiles.

CAS 23081-12-1

1-(4-chlorophenyl)-2-mercaptoethanone

1-(4-Chlorophenyl)-2-mercaptoethanone

Ref: TR-C377855