76883-69-7

Basic information

• Product Name: Benzenesulfonamide, N-(4-acetylphenyl)-
• CAS NO: 76883-69-7
• Molecular Formula: C14H13NO3S
• Molecular Weight: 275.328
• Mol File: 76883-69-7.mol
• Article Data: 27

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-(4-acetylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-(4-acetylphenyl)-(76883-69-7)
• EPA Substance Registry System: Benzenesulfonamide, N-(4-acetylphenyl)-(76883-69-7)

Safety Data

• Hazardous Substances Data: 76883-69-7(Hazardous Substances Data)

Upstream product

• 100-19-6 (4-nitrophenyl)ethanone 
• 98-80-6 phenylboronic acid 
• 873-55-2 sodium benzenesulfonate 
• 99-92-3 p-aminobenzophenone 
• 98-10-2 benzenesulfonamide 
• 99-90-1 para-bromoacetophenone 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 109171-57-5 N-[4-(3-phenyl-acryloyl)-phenyl]-benzenesulfonamide 
• 139571-30-5 N-{4-[(E)-3-(3-Nitro-phenyl)-acryloyl]-phenyl}-benzenesulfonamide 
• 139571-31-6 N-(4-(3-(2-chlorophenyl)acryloyl)phenyl)benzenesulfonamide 
• 109171-58-6 N-[4-(3-(4-chlorophenyl)-acryloyl)-phenyl]-benzenesulfonamide 
• 139571-24-7 N-{4-[(E)-3-(4-Amino-phenyl)-acryloyl]-phenyl}-benzenesulfonamide 
• 63421-73-8 4-Benzolsulfonamido-1-benzoylchlorid 

Relevant articles and documents

The discrete role of chlorine substitutions in the conformation and supra-molecular architecture of aryl-sulfonamides

Two aryl-sulfonamide derivatives, N-(4-acetyl-phen-yl)benzene-sulfonamide, C14H13NO3S, and N-(4-acetyl-phen-yl)-2,5-di- chloro-benzene-sulfonamide, C14H11Cl2NO 3S, differing by t

Sequential C-S and S-N Coupling Approach to Sulfonamides

A one-pot three-component reaction involving nitroarenes, (hetero)arylboronic acids, and potassium pyrosulfite leading to sulfonamides was described. A broad range of sulfonamides bearing different reactive functional groups were obtained in good to excellent yields through sequential C-S and S-N coupling that does not require metal catalysts.

Synthesis of N-arylsulfonamides through a Pd-catalyzed reduction coupling reaction of nitroarenes with sodium arylsulfinates

A novel one-step direct reductive coupling reaction between nitroarenes and sodium arylsulfinates was realized in the presence of an inexpensive Pd/C catalyst. In this procedure, readily available nitroarenes are employed as the nitrogen sources, and sodium arylsulfinates serve as both coupling partners and reductants. The method features high efficiency by using cheap Pd/C with low catalyst loading and good functional group tolerance in the absence of any additional reductants or ligands. This facile and mild synthetic method enables the high efficiency synthesis of functionalized N-arylsulfonamides from readily available substrates.