7744-25-4

Basic information

• Product Name: 1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one
• Synonyms: 1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one
• CAS NO: 7744-25-4
• Molecular Weight: 239.295
• Mol File: 7744-25-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one(7744-25-4)
• EPA Substance Registry System: 1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one(7744-25-4)

Safety Data

• Hazardous Substances Data: 7744-25-4(Hazardous Substances Data)

Upstream product

• 675-20-7 piperidin-2-one 
• 98-09-9 benzenesulfonyl chloride 
• 5693-62-9 2,3,4,5-tetrahydro-6-methoxypyridine 

Downstream Products

• 152297-90-0 N-benzenesulfonyl-3-phenylthio-2-piperidone 
• 5033-23-8 1-(phenylsulfonyl)piperidine 
• 221526-47-2 1,1-dimethylethyl (4S)-4-[(RS)-[(3RS)-3-benzenesulfonyl-2-oxopiperidin-3-yl]hydroxymethyl]-2,2-dimethyloxazolidine-3-carboxylate 
• 221526-71-2 (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one 
• 1283601-22-8 methyl 1-(benzensulfonyl)-2-oxo-1,2,5,6-tetrahydropyridine-3-carboxylate 
• 1394833-76-1 diphenyl (1-(phenylsulfonyl)-1,4,5,6-tetrahydropyridin-2-yl)phosphate 

Relevant articles and documents

Reactivity and stereoselectivity of the Diels-Alder reaction using cyclic dienophiles and siloxyaminobutadienes

Several bicyclic compounds were synthesized by the Diels-Alder reaction using aminodiene and a cyclic dienophile. The stereochemistries of the obtained adducts were determined by X-ray crystallography or NMR analysis. The stereoselectivity of this Diels-A

EFFICIENT MICHAEL ADDITION REACTIONS OF THE N-ARYLSULFONYL-3-PHENYLTHIOPIPERIDONES. SYNTHESIS OF 3-SUBSTITUTED DIHYDROPYRIDINONES

Efficient methods for the Michael addition reactions of N-arylsulfonyl-3-phenylthiopiperidones (1) with both the protected amidoacrylates (4, 9) and the simple acrylates (12) have been developed.These reactions offer an efficient route to the 3-alkyl-substituted dihydropyridinones (3, 11), the dienophiles employed in the natural product synthesis.