2524-78-9

Usage

Uses

Used in Research Applications:
3-Acetamidothioanisole is used as a chemical compound for research purposes, particularly in the field of organic chemistry. Its unique structure with a sulfur atom and an acetamido group makes it a valuable subject for studying chemical reactions and interactions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-Acetamidothioanisole is used as a potential precursor or intermediate in the synthesis of various drug molecules. Its specific role in drug development is still under investigation, but its presence in specialized databases and scientific literature indicates its importance in the field.
Used in Chemical Synthesis:
3-Acetamidothioanisole is employed as a reagent in the synthesis of other organic compounds. Its versatility in chemical reactions allows it to be a key component in the creation of new molecules with potential applications in various industries.

InChI:InChI=1/C9H11NOS/c1-7(11)10-8-4-3-5-9(6-8)12-2/h3-6H,1-2H3,(H,10,11)

Upstream product

• 23905-47-7 bis-(3-acetylamino-phenyl)-disulfide 
• 861377-83-5 acetic acid-(3-methanesulfinyl-anilide) 
• 1783-81-9 3-methylmercaptoaniline 
• 108-24-7 acetic anhydride 

Downstream Products

• 58202-85-0 acetic acid-(3-methanesulfonyl-anilide) 
• 861377-83-5 acetic acid-(3-methanesulfinyl-anilide) 
• 861613-19-6 acetic acid-(2,4-dichloro-5-trichloromethylsulfanyl-anilide) 
• 94855-95-5 3-methylsulfanyl-aniline; hydrochloride 
• 73568-30-6 2-chloro-7-methylsulfanyl-quinoline-3-carbaldehyde 
• 19185-64-9 3-Methylmercapto-4-sulfamoyl-acetanilid 
• 39082-89-8 3(R,S)-(methylsulphinyl)aniline 
• 80213-28-1 3-methylsulfonylaniline hydrochloride 
• 19185-65-0 3-Methylsulfonyl-4-sulfamoyl-acetanilid 

Relevant academic research and scientific papers

Synthesis and Herbicidal Activity of Triketone-Quinoline Hybrids as Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors

4-Hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27, HPPD) is one of the most important targets for herbicide discovery. In the search for new HPPD inhibitors with novel scaffolds, triketone-quinoline hybrids were designed and subsequently optimized on the basis of the structure-activity relationship (SAR) studies. Most of the synthesized compounds displayed potent inhibition of Arabidopsis thaliana HPPD (AtHPPD), and some of them exhibited broad-spectrum and promising herbicidal activity at the rate of 150 g ai/ha by postemergence application. Most promisingly, compound III-l, 3-hydroxy-2-(2-methoxy-7-(methylthio)quinoline-3-carbonyl)cyclohex-2-enone (Ki = 0.009 ～M, AtHPPD), had broader spectrum of weed control than mesotrione. Furthermore, compound III-l was much safer to maize at the rate of 150 g ai/ha than mesotrione, demonstrating its great potential as herbicide for weed control in maize fields. Therefore, triketone-quinoline hybrids may serve as new lead structures for novel herbicide discovery.

Hydrogenation of sulfoxides to sulfides under mild conditions using ruthenium nanoparticle catalysts

The first demonstration of the hydrogenation of sulfoxides under atmospheric H2 pressure is reported. The highly efficient reaction is facilitated by a heterogeneous Ru nanoparticle catalyst. The mild reaction conditions enable the selective hydrogenation of a wide range of functionalized sulfoxides to the corresponding sulfides. The high redox ability of RuO x nanoparticles plays a key role in the hydrogenation.