CAS 4371-23-7

[1,1'-Biphenyl]-4-sulfonamide

Description:

[1,1'-Biphenyl]-4-sulfonamide, with the CAS number 4371-23-7, is an organic compound characterized by the presence of a biphenyl structure substituted with a sulfonamide group at the para position. This compound typically exhibits a solid state at room temperature and is known for its stability under standard conditions. It is generally soluble in polar organic solvents, while its solubility in water is limited due to the hydrophobic nature of the biphenyl moiety. The sulfonamide functional group imparts certain chemical reactivity, making it useful in various applications, including pharmaceuticals and agrochemicals. The compound may exhibit biological activity, potentially acting as an inhibitor or modulator in biochemical pathways. Its properties, such as melting point, boiling point, and specific reactivity, can vary based on purity and environmental conditions. As with many sulfonamides, it is important to handle this compound with care, considering potential health and safety implications associated with sulfonamide derivatives.

Formula: C₁₂H₁₁NO₂S

[1,1′-Biphenyl]-4-sulfonamide

CAS: 4371-23-7

Formula: C₁₂H₁₁NO₂S

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 233.29

Ref: 10-F458601

4-Phenylbenzene-1-sulfonamide

CAS: 4371-23-7

4-Phenylbenzenesulfonamide (4PBSA) is a phenoxy compound that binds to the active site of histone deacetylase and inhibits its activity. It has been shown that 4PBSA can inhibit acetylation at nanomolar concentrations and it may be an effective treatment for cancer. The effects of 4PBSA were studied in two different assays, one using cisplatin and the other using nitro. Nitro was found to have a more potent effect than cisplatin, but both compounds had similar results in the assays. 4PBSA has also been shown to be an estrogen receptor antagonist, which may explain some of its anticancer properties. This drug may also inhibit DNA replication by binding to human estrogen receptors and preventing transcriptional activation.

Formula: C₁₂H₁₁NO₂S

Purity: Min. 95%

Molecular weight: 233.29 g/mol

Ref: 3D-EAA37123