850998-07-1

Basic information

• Product Name: Butanamide, 2-[bis(ethylthio)methylene]-N-(2-methylphenyl)-3-oxo-
• CAS NO: 850998-07-1
• Molecular Formula: C16H21NO2S2
• Molecular Weight: 323.48
• Mol File: 850998-07-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Butanamide, 2-[bis(ethylthio)methylene]-N-(2-methylphenyl)-3-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanamide, 2-[bis(ethylthio)methylene]-N-(2-methylphenyl)-3-oxo-(850998-07-1)
• EPA Substance Registry System: Butanamide, 2-[bis(ethylthio)methylene]-N-(2-methylphenyl)-3-oxo-(850998-07-1)

Safety Data

• Hazardous Substances Data: 850998-07-1(Hazardous Substances Data)

Upstream product

• 75-15-0 carbon disulfide 
• 93-68-5 3-oxo-N-o-tolylbutanamide 
• 885517-59-9 2-[bis(butylthio)methylene]-3-oxo-N-o-tolylbutanamide 
• 885517-60-2 2-acetyl-3,3-bis-allylsulfanyl-N-o-tolyl-acrylamide 
• 875778-80-6 2-[bis(benzylthio)methylene]-3-oxo-N-o-tolylbutanamide 
• 74-96-4 ethyl bromide 

Downstream Products

• 10271-55-3 2-(ethylthio)-1-phenylethanone 
• 16621-37-7 2-ethylmercapto-1-methyl-ethanol 
• 23451-56-1 2-(ethylthio)-1-phenylethanol 
• 23451-57-2 2-(ethylthio)-2-phenylethanol 
• 875778-80-6 2-[bis(benzylthio)methylene]-3-oxo-N-o-tolylbutanamide 
• 885517-60-2 2-acetyl-3,3-bis-allylsulfanyl-N-o-tolyl-acrylamide 
• 885517-59-9 2-[bis(butylthio)methylene]-3-oxo-N-o-tolylbutanamide 
• 52264-86-5 2-(benzylsulfanyl)-1-(4-methylphenyl)ethanone 
• 1373267-91-4 (4?tert?butylbenzyl)benzyl sulfide 
• 2408-88-0 2-benzylsulfanyl-1-phenylethanone 
• 31593-31-4 2-(benzylthio)-1-(4-phenylphenyl)ethanone 
• 5184-47-4 benzyl butyl sulfide 
• 22336-59-0 benzyl propyl sulfide 
• 101561-50-6 benzyl 2-methylprop-2-en-1-yl sulfide 

Relevant articles and documents

An efficient and odorless synthesis of thioethers using 2-[Bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides as thiol equivalents

Using 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides 1 as odorless thiol equivalents, an efficient and odorless synthesis of thioethers has been developed. Promoted by NaOH in EtOH, the cleavage of 1 commences to generate thiolate anions, and the generated thiolate anions then react with halides to give various thioethers in good yield. It is noteworthy that only a very faint odor of thiols can be perceived during both the reaction and the workup. Using 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides as odorless thiol equivalents, an efficient and odorless synthesis of thioethers has been developed. Promoted by NaOH in EtOH, the cleavage of 2-[bis(alkylthio)methylene] -3-oxo-N-o-tolylbutanamides commences to generate thiolate anions, and the generated thiolate anions then react with halides to give various thioethers in good yield. Copyright

[5 + 1] Annulation: A synthetic strategy for highly substituted phenols and cyclohexenones

A novel [5 + 1] annulation strategy is developed for the synthesis of highly substituted phenols and cyclohexenones from α-alkenoyl ketenedithioacetals and nitroalkanes. Copyright