2,2-Dichloro-N-[(1R)-3-chloro-1-hydroxy-1-(4-methylsulfonylphenyl)propan-2-yl]acetamide is a synthetic organic compound characterized by its complex structure, which includes multiple functional groups such as amides, chlorines, and a sulfonyl group. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of hydroxyl and amide functionalities. Its molecular structure suggests potential biological activity, possibly as a pharmaceutical agent, given the presence of the chiral center and the sulfonyl group, which can enhance interactions with biological targets. The dichloro substitution may influence its reactivity and stability, making it of interest in medicinal chemistry. Safety data and handling precautions should be observed, as compounds with halogenated groups can exhibit toxicity or environmental persistence. Overall, this compound's unique characteristics make it a subject of interest in research and development within the fields of chemistry and pharmacology.

2,2-dichloro-N-[(1R)-3-chloro-1-hydroxy-1-(4-methylsulfonylphenyl)propan-2-yl]acetamide

1322625-10-4: 2,2-Dichloro-N-[(1R)-3-chloro-1-hydroxy-1-(4-methylsulfonylphenyl)propan-2-yl]acetamide is a synthetic organic compound characterized by its complex structure, which includes multiple functional groups such as amides, chlorines, and a sulfonyl group. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of hydroxyl and amide functionalities. Its molecular structure suggests potential biological activity, possibly as a pharmaceutical agent, given the presence of the chiral center and the sulfonyl group, which can enhance interactions with biological targets. The dichloro substitution may influence its reactivity and stability, making it of interest in medicinal chemistry. Safety data and handling precautions should be observed, as compounds with halogenated groups can exhibit toxicity or environmental persistence. Overall, this compound's unique characteristics make it a subject of interest in research and development within the fields of chemistry and pharmacology.

<p>Applications An analog of Florfenicol (F405750).<br></p>

CAS 1322625-10-4

2,2-dichloro-N-[(1R)-3-chloro-1-hydroxy-1-(4-methylsulfonylphenyl)propan-2-yl]acetamide

Florfenicol Chloro Analogue

Ref: TR-F405775

Florfenicol Chloro Analogue

Ref: ST-EA-CP-F37004