875778-80-6

Basic information

• Product Name: Butanamide, 2-[bis[(phenylmethyl)thio]methylene]-N-(2-methylphenyl)-3-oxo-
• CAS NO: 875778-80-6
• Molecular Formula: C26H25NO2S2
• Molecular Weight: 447.622
• Mol File: 875778-80-6.mol

Chemical Properties

• CAS DataBase Reference: Butanamide, 2-[bis[(phenylmethyl)thio]methylene]-N-(2-methylphenyl)-3-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanamide, 2-[bis[(phenylmethyl)thio]methylene]-N-(2-methylphenyl)-3-oxo-(875778-80-6)
• EPA Substance Registry System: Butanamide, 2-[bis[(phenylmethyl)thio]methylene]-N-(2-methylphenyl)-3-oxo-(875778-80-6)

Safety Data

• Hazardous Substances Data: 875778-80-6(Hazardous Substances Data)

Upstream product

• 75-15-0 carbon disulfide 
• 93-68-5 3-oxo-N-o-tolylbutanamide 
• 100-39-0 benzyl bromide 
• 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 
• 145508-26-5 2-(bis(methylthio)methylene)-3-oxo-N-(o-tolyl)butanamide 
• 850998-07-1 2-acetyl-3,3-bis-ethylsulfanyl-N-o-tolyl-acrylamide 

Downstream Products

• 5452-33-5 (+/-)-3-benzylsulfanyl-1,3-diphenylpropan-1-one 
• 2408-88-0 2-benzylsulfanyl-1-phenylethanone 
• 5877-10-1 (RS)-1-benzylthiopropan-2-ol 
• 838-67-5 2-benzylsulfanyl-1-phenylethan-1-ol 
• 117037-28-2 1-(1-phenyl-2-hydroxy) ethyl-benzyl sulfide 
• 56155-49-8 (+/-)-trans-1-benzylsulfanyl-cyclohexanol-⁽²⁾ 
• 850998-07-1 2-acetyl-3,3-bis-ethylsulfanyl-N-o-tolyl-acrylamide 
• 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 
• 93-68-5 3-oxo-N-o-tolylbutanamide 
• 104330-53-2 ethyl 3-(o-toluidino)-3-oxopropanoate 
• 1492-49-5 benzylthiolate anion 
• 5184-47-4 benzyl butyl 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

Thia-Michael addition reactions using 2-[bis(alkylthio)methylene]-3-oxo-N- o-tolylbutanamides as odorless and efficient thiol equivalents

A series of 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides 1 have been investigated as nonthiolic and odorless thiol equivalents in thia-Michael addition reactions. The cleavage of compounds 1 is initiated by NaOH in EtOH; the in situ generated th

A clean, facile and practical synthesis of α-oxoketene S,S-acetals in water

A clean, facile and practical synthesis of α-oxoketene S,S-acetals in water has been developed. Catalyzed by tetrabutylammonium bromide (TBAB) at room temperature in water, a range of β-dicarbonyl compounds have been converted to the corresponding α-oxoke