316354-21-9

Basic information

• Product Name: 2(1H)-Pyridinone, 3-hydroxy-1-[(4-methylphenyl)sulfonyl]-
• CAS NO: 316354-21-9
• Molecular Formula: C12H11NO4S
• Molecular Weight: 265.29
• Mol File: 316354-21-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2(1H)-Pyridinone, 3-hydroxy-1-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Pyridinone, 3-hydroxy-1-[(4-methylphenyl)sulfonyl]-(316354-21-9)
• EPA Substance Registry System: 2(1H)-Pyridinone, 3-hydroxy-1-[(4-methylphenyl)sulfonyl]-(316354-21-9)

Safety Data

• Hazardous Substances Data: 316354-21-9(Hazardous Substances Data)

Upstream product

• 141667-31-4 3-[(tert-butyl)dimethylsilyloxy]-1-[(4-methylphenyl)sulfonyl]-1H-pyridin-2-one 
• 141667-58-5 3-<(tert-butyldimethylsilyl)oxy>-2-pyridone 
• 98-59-9 p-toluenesulfonyl chloride 
• 84719-32-4 3-Hydroxy-2(1H)-pyridinone 
• 16867-04-2 dihydroxypyridine 

Downstream Products

• 691012-97-2 1-(4% Methylbenzenesulfonyl)-3-hydroxy-4-(pyrrolidin-1-ylmethyl)pyridin-2(1H)-one 
• 676566-77-1 (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl (1R,4S,5R)-4-(methoxymethoxy)-2-[(4-methylphenyl)sulfonyl]-3-oxo-2-azabicyclo[2.2.2]oct-7-ene-5-carboxylate 

Relevant articles and documents

A base-catalyzed Diels-Alder reaction of N-tosyl-3-hydroxy-2-pyridone

A Diels-Alder reaction of N-tosyl-3-hydroxy-2-pyridone with an electron deficient dienophile was catalyzed by base. The reactivity, stereoselectivity and mechanism of this reaction are described. (C) 2000 Elsevier Science Ltd.

N-sulfonyl-4-methyleneamino-3-hydroxy-2-pyridones

Compounds of Formula (I) are effective in the treatment of a microbial infection.

β-Glycosidase inhibitors mimicking the pyranoside boat conformation

Polyhydroxylated isoquinuclidines mimicking the boat conformation of pyranosides are strong and selective inhibitors of a retaining β-mannosidase.