16761-19-6

Upstream product

• 121-60-8 p-acetylaminobenzenesulfonyl chloride 
• 71905-93-6 acetylaminobenzenesulfonylchloride 

Downstream Products

• 39234-94-1 4-acetylamino-3-nitro-benzenesulfonic acid amide 
• 631911-38-1 4-(4-amino-3-nitro-benzenesulfonyl)-5-methylsulfanyl-thiophene-2-carboxylic acid methyl ester 
• 39234-96-3 4-amino-3-bromo-5-nitrobenzenesulfonamide 
• 93534-94-2 3-amino-4-hydroxy-N-pyridin-2-yl-benzenesulfonamide 
• 145764-14-3 4-amino-3-nitro-benzenesulfonic acid-[2]pyridylamide 
• 92316-16-0 4-hydroxy-3-nitro-N-pyridin-2-yl-benzenesulfonamide 
• 2360-19-2 4-amino-3-nitrobenzenesulfonamide 
• 24855-58-1 4-hydroxy-3-nitrobenzenesulfonamide 

Relevant academic research and scientific papers

ORGANIC COMPOUND, CRYSTAL DIELECTRIC LAYER AND CAPACITOR BACKGROUND

The present disclosure provides an organic compound characterized by electronic polarizability and having a following general structural formula: where Core is an aromatic polycyclic conjugated molecule, R1 is group providing solubility of the

The Preparation of Sodium 4-Amino-3-nitrobenzenesulfonate and Some Related Compounds

The sodium salt of 4-amino-3-nitrobenzenesulfonic acid (o-nitroaniline-p-sulfonic acid) has been prepared by the action of dilute sodium hydroxide solution on ethyl carbamate.Central to this synthesis is the finding that the N-ethoxycarbonyl group, when located ortho to a nitro group (but not to a bromo group), is readily removed by dilute sodium hydroxide solution.

Substituted benzenesulfonamides as anthelmintics

This invention relates to a novel method for the treatment of parasitic diseases and the compositions used in said treatment. More specifically this invention relates to benzenesulfonamides substituted at the 3, 4, and 5 positions of the benzene ring and to the use of such compounds for the treatment of mature and immature liver fluke infections.