929083-19-2

Basic information

• Product Name: Ethanone, 1-[2-[(1,1-dimethylethyl)thio]phenyl]-
• CAS NO: 929083-19-2
• Molecular Formula: C12H16OS
• Molecular Weight: 208.324
• Mol File: 929083-19-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-[(1,1-dimethylethyl)thio]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-[(1,1-dimethylethyl)thio]phenyl]-(929083-19-2)
• EPA Substance Registry System: Ethanone, 1-[2-[(1,1-dimethylethyl)thio]phenyl]-(929083-19-2)

Safety Data

• Hazardous Substances Data: 929083-19-2(Hazardous Substances Data)

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 articles and documents

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

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.