929083-19-2

Upstream product

• 2142-68-9 1-(2-chlorophenyl)ethanone 
• 75-66-1 2-methylpropan-2-thiol 
• 2142-69-0 2-bromophenyl methyl ketone 
• 29364-29-2 sodium tert-butyl thiolate 

Downstream Products

• 1192716-61-2 (1-tert-butylsulfanyl)-2-(2,2-dichloro-1-methylvinyl)benzenethiol 
• 1402911-76-5 2-(3,4-dichlorophenyl)-4H-thiochromen-4-one 
• 1402911-77-6 2-(2,5-dimethoxyphenyl)thiochromen-4-one 
• 784-62-3 1-thioflavone 
• 1402911-70-9 3-(1,3-benzodioxol-5-yl)-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1-one 
• 1402911-71-0 1-[2-(1,1-dimethylethylsulfanyl)phenyl]-3-(naphthalen-1-yl)prop-2-en-1-one 
• 1402911-67-4 1-[2-(1,1-dimethylethylsulfanyl)phenyl]-3-phenylprop-2-en-1-one 
• 1402911-69-6 3-(2,5-dimethoxyphenyl)-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1-one 
• 1402911-68-5 3-(3,4-dichlorophenyl)-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1-one 
• 26824-02-2 1-(2-mercaptophenyl)ethan-1-one 

Relevant academic research and scientific papers

Metal-free visible light-promoted synthesis of isothiazoles: A catalytic approach for N-S bond formation from iminyl radicals under batch and flow conditions

A sustainable synthesis of isothiazoles has been developed using an α-amino-oxy acid auxiliary and applying photoredox catalysis. This simple strategy features mild conditions, broad scope and wide functional group tolerance representing a new enviromenta

Substituted Benzothietes: Synthesis and a Quantum Chemical Investigation of Their Cycloreversion Properties

A flexible synthesis for highly substituted benzothietes that does not require flash-vacuum pyrolysis was developed. This allows for the use of a number of functional groups and nonvaporizable molecules. Highly stabilized derivatives were isolated. The molecular orbital properties of various benzothietes were evaluated by density functional methods. The mechanism of the cycloreversion of the four-membered ring was compared to that of the oxygen-containing analogues.

A convenient synthesis of 2-arylthiochromen-4-ones (thioflavones) by iodine-mediated cyclization of 3-aryl-1-[2-(1,1-dimethylethylsulfanyl)phenyl] prop-2-en- 1-ones

A convenient two-step synthesis of 2-arylthiochromen-4-ones (thioflavones) beginning with 1-[2-(1,1-dimethylethylsulfanyl)phenyl]ethanones is described. Thus, 3-aryl-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1- ones were prepared by the condensation of 1-[2-(1,1- dimethylethylsulfanyl)phenyl] ethanones with aromatic aldehyde in the presence of sodium hydroxide, and were treated with iodine in refluxing N-methylpyrrolidin-2-one (NMP) or propanenitrile to afford the desired products in moderate to fair yields.