296273-08-0

Basic information

• Product Name: Benzenesulfonamide, N-(2-iodophenyl)-4-nitro-
• CAS NO: 296273-08-0
• Molecular Formula: C12H9IN2O4S
• Molecular Weight: 404.185
• Mol File: 296273-08-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-(2-iodophenyl)-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-(2-iodophenyl)-4-nitro-(296273-08-0)
• EPA Substance Registry System: Benzenesulfonamide, N-(2-iodophenyl)-4-nitro-(296273-08-0)

Safety Data

• Hazardous Substances Data: 296273-08-0(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 62-53-3 aniline 

Downstream Products

• 900537-30-6 N-(2-iodophenyl)-N-methyl-4-nitrobenzenesulfonamide 
• 1433218-75-7 N-(2-bromoethyl)-N-(2-iodophenyl)-4-nitrobenzenesulfonamide 
• 22191-17-9 C₁₄H₁₂N₂O₄S₂ 
• 57056-93-6 N-methyl-2-iodoaniline 
• 3406-75-5 2-(4-nitrophenylthio)acetic acid 

Relevant articles and documents

Deacetylative Aryl Migration of Diaryliodonium Salts with C(sp2)-N Bond Formation toward ortho-Iodo N-Aryl Sulfonamides

An unprecedented approach of metal-free C(sp2)-N bond formation via deacetylation/intramolecular aryl migration is demonstrated with novel N-sulfonamide substituted diaryliodonium salts. The reaction provides a variety of ortho-iodo N-aryl sulf

Isothiourea-Catalyzed Atroposelective N-Acylation of Sulfonamides

We report herein an atroposelective N-acylation of sulfonamides using a commercially available isothiourea catalyst, (S)-HBTM, with a simple procedure. The N-sulfonyl anilide products can be obtained in good to high enantiopurity, which represents a new axially chiral scaffold. The application of the product as a chiral iodine catalyst is also demonstrated for the asymmetric α-oxytosylation of propiophenone.

Synthesis of 11a- N -Arylsulfonyl-5-carbapterocarpans (Tetrahydro-5 H -benzo[ a ]carbazoles) by Azaarylation of Dihydronaphthalenes with o -Iodo- N -(Arylsulfonyl)anilines in Poly(ethylene glycol)

11a-N-Arylsulfonyl-5-carbapterocarpans (tetrahydro-5H-benzo[a]carbazoles) were synthesized by palladium-catalyzed azaarylation of dihydronaphthalenes with o-iodo-N-(arylsulfonyl)anilines in poly(ethylene glycol) (PEG-400). Better chemical yields (moderate