175178-88-8

Upstream product

• 3405-88-7 (4-chlorophenylthio)acetic acid 
• 14752-66-0 sodium p-chlorobenzenesulphinate 
• 3405-89-8 2-(4-chloro-phenylsulfonyl)acetic acid 
• 637-39-8 triethanolamine hydrochloride 
• 95153-86-9 sodium salt of the 4-chloro-benzenesulfonyl-acetic acid 
• 102-71-6 triethanolamine 

Relevant academic research and scientific papers

New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium

Physiologically and pharmacologically active het(aryl)chalcogenylacetates of tris(2-hydroxyethyl)ammonium of pharmacopeial purity have been synthesized by the reaction of het(aryl)chalcogenylacetic acids with sodium (potassium) hydroxide and triethanolami

Synthesis and Pharmacological Activity of Tris(2-hydroxyethyl)ammonium 4-Chlorophenylsulfonylacetate

Methods for the synthesis of 4-chlorophenylsulfonylacetic acid and its tris(2-hydroxyethyl)ammonium salt (“sulfacetamine”) were studied. The results of in vitro and in vivo experiments showed that sulfacetamine possesses high antithrombotic, antioxidant, hypocholesterolemic, immunostimulating, and protective-adaptive activities.

Tris(2-hydroxyethyl)ammonium arylchalcogenylacetates, growth stimulants of alcohol yeast Saccharomyces cerevisiae

A number of tris(2-hydroxyethyl)ammonium arylchalcogenylacetates ArYCH2CO2 –? ?HN+(CH2CH2OH)3 (1—4) (Ar = aryl; Y = O, S, SO2) were synthesized. Their structure was es