885517-59-9

Basic information

• Product Name: Butanamide, 2-[bis(butylthio)methylene]-N-(2-methylphenyl)-3-oxo-
• CAS NO: 885517-59-9
• Molecular Formula: C20H29NO2S2
• Molecular Weight: 379.588
• Mol File: 885517-59-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Butanamide, 2-[bis(butylthio)methylene]-N-(2-methylphenyl)-3-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanamide, 2-[bis(butylthio)methylene]-N-(2-methylphenyl)-3-oxo-(885517-59-9)
• EPA Substance Registry System: Butanamide, 2-[bis(butylthio)methylene]-N-(2-methylphenyl)-3-oxo-(885517-59-9)

Safety Data

• Hazardous Substances Data: 885517-59-9(Hazardous Substances Data)

Upstream product

• 109-65-9 1-bromo-butane 
• 75-15-0 carbon disulfide 
• 93-68-5 3-oxo-N-o-tolylbutanamide 
• 885517-60-2 2-acetyl-3,3-bis-allylsulfanyl-N-o-tolyl-acrylamide 
• 145508-26-5 2-(bis(methylthio)methylene)-3-oxo-N-(o-tolyl)butanamide 
• 875778-80-6 2-[bis(benzylthio)methylene]-3-oxo-N-o-tolylbutanamide 
• 850998-07-1 2-acetyl-3,3-bis-ethylsulfanyl-N-o-tolyl-acrylamide 

Downstream Products

• 850998-07-1 2-acetyl-3,3-bis-ethylsulfanyl-N-o-tolyl-acrylamide 
• 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 
• 52264-86-5 2-(benzylsulfanyl)-1-(4-methylphenyl)ethanone 
• 1373267-91-4 (4?tert?butylbenzyl)benzyl sulfide 
• 2408-88-0 2-benzylsulfanyl-1-phenylethanone 
• 6306-17-8 butyl phenacyl sulfide 
• 93-68-5 3-oxo-N-o-tolylbutanamide 
• 22598-79-4 trans-(2-hydroxycyclohexyl)-n-butyl sulfide 
• 138842-20-3 1-(1-phenyl-2-hydroxy) ethyl-n-butyl sulfide 
• 53408-89-2 2-(butylthio)-1-methylethan-1-ol 
• 21205-11-8 1,3-diphenyl-3-(butylthio)propan-1-one 

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