4'-Acetyl-4-biphenylsulfonyl chloride, with the CAS number 144006-69-9, is an organic compound characterized by its sulfonyl chloride functional group, which is known for its reactivity in various chemical transformations. This compound features a biphenyl structure, indicating the presence of two phenyl rings connected by a single bond, and an acetyl group, which contributes to its chemical properties. The sulfonyl chloride moiety makes it a potent electrophile, allowing it to participate in nucleophilic substitution reactions, often used in the synthesis of sulfonamides and other derivatives. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the acetyl group can influence its reactivity and stability, making it useful in various synthetic applications in organic chemistry. As with many sulfonyl chlorides, it should be handled with care due to its potential to release hydrochloric acid upon reaction and its reactivity towards moisture, which can lead to hydrolysis.

4'-Acetyl-4-biphenylsulfonyl chloride

144006-69-9: 4'-Acetylbiphenyl-4-sulfonyl chloride, [1,1'-Biphenyl]-4-sulfonyl chloride, 4'-acetyl-, 4-(4-Acetylphenyl)Benzenesulfonyl Chloride

CAS 144006-69-9: 4'-Acetyl-4-biphenylsulfonyl chloride

[1,1'-Biphenyl]-4-sulfonyl chloride, 4'-acetyl-

Ref: IN-DA001IRH

4'-Acetylbiphenyl-4-sulfonyl chloride

Ref: 10-F014905