162600-08-0

Basic information

• Product Name: ethyl 3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside
• Synonyms: ethyl 3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside
• CAS NO: 162600-08-0
• Molecular Weight: 494.652
• Mol File: 162600-08-0.mol

Chemical Properties

• CAS DataBase Reference: ethyl 3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside(162600-08-0)
• EPA Substance Registry System: ethyl 3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside(162600-08-0)

Safety Data

• Hazardous Substances Data: 162600-08-0(Hazardous Substances Data)

Upstream product

• 30383-01-8 lithium thioethoxide 
• 112289-38-0 1,2-anhydro-3,4,6-tri-O-benzyl-D-galactopyranose 
• 80040-79-5 3,4,6-tri-O-benzyl-D-galactal 
• 100-39-0 benzyl bromide 
• 162466-43-5 ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 145852-76-2 3,6-di-O-benzyl-D-glucal 

Downstream Products

• 169151-44-4 ethyl-2-O-benzoyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 162606-13-5 N-[(2R,3R,4R,5S,6R)-4-Benzyloxy-6-benzyloxymethyl-5-((2S,3R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-2-methoxy-tetrahydro-pyran-3-yl]-acetamide 
• 259871-12-0 ethyl 2-O-[1-O-methyl-4,6-O-(1,1,3,3-tetraisopropyl-1,3-disiloxane-1,3-diyl)-α-D-mannopyranos-3-yloxycarbonylpropanoyl]-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 616861-51-9 methyl (2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->2)-(allyl 3,4-di-O-methoxymethyl-β-D-glucopyranosid)uronate 
• 616861-53-1 methyl (3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->2)-(allyl 3,4-di-O-methoxymethyl-β-D-glucopyranosid)uronate 
• 162466-43-5 ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 

Relevant articles and documents

Conversion of D-Glucals into L-Glycals and Mirror-Image Carbohydrates

(Equation presented) L-Glycals can be prepared in seven steps from readily available D-glucals, enabling the facile construction of mirror-image carbohydrates such as the L-lactosamine derivative shown above.

Comparative solution and solid-phase glycosylations toward a disaccharide library

A comparative study on solution-phase and solid-phase oligosaccharide synthesis was performed. A 16-member library containing all regioisomers of Glc-Glc, Glc-Gal, Gal-Glc, and Gal-Gal disaccharides was synthesized both in solution and on solid phase. The