22437-44-1

Basic information

• Product Name: Propanamide, 2-methyl-3-(phenylthio)-
• CAS NO: 22437-44-1
• Molecular Formula: C10H13NOS
• Molecular Weight: 195.285
• Mol File: 22437-44-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Propanamide, 2-methyl-3-(phenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanamide, 2-methyl-3-(phenylthio)-(22437-44-1)
• EPA Substance Registry System: Propanamide, 2-methyl-3-(phenylthio)-(22437-44-1)

Safety Data

• Hazardous Substances Data: 22437-44-1(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 79-39-0 Methacrylamide 

Downstream Products

• 138428-89-4 N-benzyl-2-methyl-3-(phenylthio)propionamide 
• 125606-52-2 2-methyl-3-(phenylsulfinyl)propionamide 
• 125606-53-3 N-benzyl-2-methyl-3-(phenylsulfinyl)propionamide 
• 125606-61-3 cis-N-benzyl-3-methyl-4-(phenylthio)azetidin-2-one 
• 125606-61-3 trans-N-benzyl-3-methyl-4-(phenylthio)azetidin-2-one 
• 125606-60-2 cis-N-(tert-butyldimethylsilyl)-3-methyl-4-(phenylthio)azetidin-2-one 
• 125606-60-2 trans-N-(tert-butyldimethylsilyl)-3-methyl-4-(phenylthio)azetidin-2-one 

Relevant articles and documents

Thio-Michael addition of α,β-unsaturated amides catalyzed by Nmm-based ionic liquids

A simple and practical thio-Michael addition of α,β-unsaturated amides catalyzed by Nmm-based ionic liquids with a 1,2-propanediol group has been developed. All the α,β-unsaturated amides without substituents at the carbon end could smoothly react with su

Chemistry of O-silylated ketene acetals: A mild and convenient synthesis of β-lactam antibiotics

β-Amido sulfoxides (1) reacted with O-silylated ketene acetal (16) in dry acetonitrile in the presence of a catalytic amount of zinc iodide to give the 4-phenylthioazetidin-2-ones (17). Oxidation of 17 with m-chloroperbenzoic acid gave the corresponding s