1419313-64-6

Basic information

• Product Name: (S)-4-methyl-N-(3-oxo-3,6-dihydro-2H-pyran-2-yl)benzenesulfonamide
• Synonyms: (S)-4-methyl-N-(3-oxo-3,6-dihydro-2H-pyran-2-yl)benzenesulfonamide
• CAS NO: 1419313-64-6
• Molecular Weight: 267.306
• Mol File: 1419313-64-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-4-methyl-N-(3-oxo-3,6-dihydro-2H-pyran-2-yl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-methyl-N-(3-oxo-3,6-dihydro-2H-pyran-2-yl)benzenesulfonamide(1419313-64-6)
• EPA Substance Registry System: (S)-4-methyl-N-(3-oxo-3,6-dihydro-2H-pyran-2-yl)benzenesulfonamide(1419313-64-6)

Safety Data

• Hazardous Substances Data: 1419313-64-6(Hazardous Substances Data)

Upstream product

• 62446-93-9 1,2,3,4-tetra-O-acetyl-D-xylopyranose 
• 87-72-9 D-Xylose 
• 14125-76-9 1,5-anhydro-2,3,4-tri-O-acetyl-D-threo-pent-1-enitol 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 1419313-76-0 C₁₈H₂₃NO₄S 

Relevant articles and documents

Ferrier-type N-glycosylation: Synthesis of N-glycosides of enone sugars

A mild and efficient protocol for the stereoselective synthesis of N-glycosides of enone sugars has been developed. The reaction proceeds to provide N-glycosides of enone sugars in moderate to good yields with preferential α-anomeric selectivity. Additionally, applications of the N-glycosides of enone sugar derivatives as precursor to assemble some biochemically functional derivatives have also been explored. This includes the use of N-glycosides of enone sugars as reactive dienophile in asymmetric synthesis of bicyclic adduct through Diels-Alder cycloaddition reaction.