667923-56-0

Basic information

• Product Name: 3-amino-5-O-benzoyl-3-C-cyano-3-deoxy-3-N-phenylmethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose
• Synonyms: 3-amino-5-O-benzoyl-3-C-cyano-3-deoxy-3-N-phenylmethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose
• CAS NO: 667923-56-0
• Molecular Weight: 472.519
• Mol File: 667923-56-0.mol

Chemical Properties

• CAS DataBase Reference: 3-amino-5-O-benzoyl-3-C-cyano-3-deoxy-3-N-phenylmethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-5-O-benzoyl-3-C-cyano-3-deoxy-3-N-phenylmethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose(667923-56-0)
• EPA Substance Registry System: 3-amino-5-O-benzoyl-3-C-cyano-3-deoxy-3-N-phenylmethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose(667923-56-0)

Safety Data

• Hazardous Substances Data: 667923-56-0(Hazardous Substances Data)

Upstream product

• 6698-46-0 5-O-benzoyl-1,2-O-isopropylidene-α-D-ribofuranos-3-ulose 
• 302582-11-2 3-amino-5-O-benzoyl-3-C-cyano-3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 
• 1939-99-7 benzenesulfonyl chloride 

Downstream Products

• 667923-36-6 3-amino-3-N-benzyl-5-O-benzoyl-3-C-cyano-3-deoxy-1,2-O-isopropylidene-3-N-phenylmethanesulfonyl-α-D-ribofuranose 
• 667923-90-2 1,2-O-isopropylidene-α-D-erythro-pentofuranose-3-spiro-3'-(4'-amino-2'-N-methyl-5'-phenyl-5'H-2',3'-dihydroisothiazole-1',1'-dioxide) 
• 667923-88-8 1,2-O-isopropylidene-α-D-erythro-pentofuranose-3-spiro-3'-(4'-amino-5'-phenyl-5'H-2',3'-dihydroisothiazole-1',1'-dioxide) 
• 667923-34-4 3-amino-5-O-benzoyl-3-C-cyano-3-deoxy-1,2-O-isopropylidene-3-N-methyl-3-N-phenylmethanesulfonyl-α-D-ribofuranose 

Relevant articles and documents

Synthesis of 4-Amino-5-H-2,3-dihydroisothiazole-1,1-dioxide Ring Systems on Sugar Templates via Carbanion-Mediated Sulfonamide Intramolecular Cyclization Reactions (CSIC Protocols) of Glyco-α-sulfonamidonitriles

The carbanion-mediated sulfonate intramolecular cyclizations (CSIC protocols) of glyco-α-sulfona-midonitriles derived from readily available monosaccharides have been extensively investigated using potassium carbonate, cesium carbonate, n-BuLi, and LDA as