7749-05-5

Usage

Uses

Used in Pharmaceutical Industry:
(1,3,2-Dithiarsolan-2-ylthio)acetic acid is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure containing arsenic atoms and a carboxylic acid group may offer novel pharmacological activities and therapeutic benefits. Further research is required to explore its potential as a drug candidate and to optimize its efficacy and safety.
Used in Materials Science:
(1,3,2-Dithiarsolan-2-ylthio)acetic acid is used as a material in materials science for its unique chemical and physical properties. Its thioarsolan structure and arsenic content may provide new opportunities for the development of advanced materials with specific characteristics and applications. Further studies are needed to investigate its potential in materials science and to identify suitable applications for (1,3,2-Dithiarsolan-2-ylthio)acetic acid.

InChI:InChI=1/C4H7AsO2S3/c6-4(7)3-10-5-8-1-2-9-5/h1-3H2,(H,6,7)

Upstream product

• 68-11-1 mercaptoacetic acid 
• 3741-32-0 2-chloro-[1,3,2]dithiarsolane 

Relevant academic research and scientific papers

Synthesis, spectroscopic, structural characterization, and antimicrobial studies of 1,3-dithia-2-arsacyclopentane derivatives with oxygen and sulfur donor ligands

Some mixed 1,3-dithia-2-arsacyclopentane derivatives with oxygen and sulfur donor ligands have been synthesized by the reaction of 2-chloro-1,3-dithia-2- arsacyclopentane and oxygen and sulfur donor ligands (benzoic acid, thiobenzoic acid, sodium acetate, thioacetic acid, phenol, thiophenol, sodium salicylate, and thioglycolic acid) in equimolar ratio (1:1) in refluxing anhydrous benzene solution. These white or yellow solids/liquids derivatives have been characterized by melting points, molecular weights, elemental analyses (C, H, S, and As), and spectroscopic [UV, IR as well as NMR (1H and 13C)] studies. Tentative structures are proposed on the basis of the spectroscopic results. The free ligands and the corresponding arsenic compounds exhibited good activities as antibacterial and antifungal agents on some selected bacterial and fungal strains. Chloroamphenicol and terbinafin were used as standards for comparison. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. Copyright Taylor & Francis Group, LLC.