153373-58-1

Basic information

• Product Name: O-(methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-(2<*>6)-2,3-di-O-acetyl-1,5-benzyloxycarbonylimino-1,5-dideoxy-D-glucitol
• Synonyms: O-(methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-(2<*>6)-2,3-di-O-acetyl-1,5-benzyloxycarbonylimino-1,5-dideoxy-D-glucitol
• CAS NO: 153373-58-1
• Molecular Weight: 854.816
• Mol File: 153373-58-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: O-(methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-(2<*>6)-2,3-di-O-acetyl-1,5-benzyloxycarbonylimino-1,5-dideoxy-D-glucitol(CAS DataBase Reference)
• NIST Chemistry Reference: O-(methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-(2<*>6)-2,3-di-O-acetyl-1,5-benzyloxycarbonylimino-1,5-dideoxy-D-glucitol(153373-58-1)
• EPA Substance Registry System: O-(methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-(2<*>6)-2,3-di-O-acetyl-1,5-benzyloxycarbonylimino-1,5-dideoxy-D-glucitol(153373-58-1)

Safety Data

• Hazardous Substances Data: 153373-58-1(Hazardous Substances Data)

Upstream product

• 153373-52-5 2,3-di-O-acetyl-4,6-O-benzylidene-1,5-benzyloxycarbonylimino-1,5-dideoxy-D-glucitol 
• 138381-83-6 4,6-O-(R-Benzylidene)-N-benzyloxycarbonyl-1,5-dideoxy-1,5-imino-D-glucitol 
• 144240-36-8 methyl (methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-D-galacto-2-nonulopyranosid)onate 
• 153373-53-6 2,3-di-O-acetyl-1,5-benzyloxycarbonylimino-1,5-dideoxy-D-glucitol 

Downstream Products

• 172139-95-6 (2R,3R,4R,5S)-3,4,5-Triacetoxy-2-[(2R,4S,5R,6R)-4-acetoxy-5-acetylamino-2-methoxycarbonyl-6-((1S,2R)-1,2,3-triacetoxy-propyl)-tetrahydro-pyran-2-yloxymethyl]-piperidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

Synthetic and structural studies of α-sialyl-(2 -> 6) and α-sialyl-(2 -> 3) 1-deoxynojirimycin derivatives potentially used for biomedical applications

Suitably protected derivatives of 1-deoxynojirimycin (1,5-dideoxy-1,5-imino-D-glucitol, DNJ) and its D-galacto analog were coupled with 2-thioglycosides of N-acetylneuraminic acid.The resulying disaccharides were converted into a variety of α-sialyl-(2 -> 6)- and α-sialyl-(2 -> 3)-DNJ derivatives, including the cyclic lactams 6-O-(5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylono-1',5-lactam)-1,5-dideoxy-1,5-imino-D-glucitol and -D-galactitol.The structural features of the synthetic compounds were investigated by ion-spray mass and 1H NMR spectrometry.The 1C4 conformation of N-tert-butoxycarbonyl-DNJ, a synthetic intermediate having the gluco configuration, was confirmed by X-ray crystallography.Keywords: Synthetic and structural studies; α-Sialyl-(2 -> 6); α-Sialyl-(2 -> 3); Deoxynojirimycin derivatives; Biomedical applications.