612-31-7

Upstream product

• 88-21-1 2-amino-1-benzenesulfonic acid 
• 64-17-5 ethanol 
• 7664-93-9 sulfuric acid 

Downstream Products

• 58734-48-8 2-ethoxy-benzenesulfonic acid 
• 209863-91-2 (S)-N,N-1,2-benzenedisulfonyl-1-phenylethylamine 
• 199605-37-3 2-(chloroseleno)benzenesulfonyl chloride 
• 6461-76-3 1,2-benzenedisulfonyl dichloride 
• 609-46-1 phenol-2-sulfonic acid 
• 39201-85-9 1-(2-Sulfoxybenzol)-3,3-dimethyltriazen 
• 34256-00-3 4-methoxyphenyl-3-sulfonic acid 

Relevant academic research and scientific papers

N,N-1,2-benzenedisulfonylimide, a new cyclic leaving group for the stereoselective nucleophilic substitution of amines

We hereby report the preparation and nucleophilic substitutions of the N,N-1,2-benzenedisulfonylimide derivatives la and 2a of the chiral amines 1 and 2. The nucleophilic attack of KNO2 afforded the respective alcohols 3 and 4 with 84-90% inversion of configuration. Nucleophilic attack by the azide ion afforded the azide products 5 and 6 which were reduced to the corresponding inverted mines 1 and 2 (94-98.5% inversion). The improved leaving group ability of the N,N-1,2-benzenedisulfonylimides compared with previously reported N,N-disulfonylimides is discussed. Chiral GLC analysis of all products is summarized and the alternative chiral analysis of product 3 by 13C NMR using heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin as a chiral solvating agent (CSA) is discussed.

Bis(2-chlorosulfonylphenyl) diselenide - the substrate for organoselenium sulfonamides

Synthesis of bis(2-chlorosulfonylphenyl) diselenide (11) from 2-amino-benzenesulfonic acid was elaborated. It was shown that (11) is a good starting material for synthesis of the organoselenium sulfonamides, such as bis(2-sulfamoylphenyl) diselenides (3)

Waste-Free Quantitative Gas/Solid Diazotation Using Nitrogen Dioxide and Triazene Synthesis, Both Avoiding Liquid Phases

Solid diazonium nitrates (2a-j) are quantitatively obtained by reaction of crystalline anilines (1a-j) with gaseous nitrogen dioxide. Solid diazonium salts react quantitatively with dimethylamine to give the triazenes (4a-j). Wastes that are typical for the previous syntheses of these compounds in solution are avoided. Atomic force microscopic (AFM) investigations indicate long-range molecular movements due to phase rebuilding. The features thus formed are related to the known crystal structures of the starting anilines. The diazotations run to completion, because, after accumulation of product molecules, phase transformation to give the product lattices leads to crystal disintegration and thus to formation of fresh surface over and over.