172471-62-4

Basic information

• Product Name: phenyl 2,3,4,6-tetra-O-methyl-1-thio-β-D-galactopyranoside
• Synonyms: phenyl 2,3,4,6-tetra-O-methyl-1-thio-β-D-galactopyranoside
• CAS NO: 172471-62-4
• Molecular Weight: 328.43
• Mol File: 172471-62-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: phenyl 2,3,4,6-tetra-O-methyl-1-thio-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 2,3,4,6-tetra-O-methyl-1-thio-β-D-galactopyranoside(172471-62-4)
• EPA Substance Registry System: phenyl 2,3,4,6-tetra-O-methyl-1-thio-β-D-galactopyranoside(172471-62-4)

Safety Data

• Hazardous Substances Data: 172471-62-4(Hazardous Substances Data)

Upstream product

• 16758-34-2 1-thiophenyl-β-D-galactopyranoside 
• 74-88-4 methyl iodide 
• 13992-16-0 1-deoxy-1-(phenylthio)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranose 
• 3353-52-4 (3R,4S,5S,6R)-3,4,5-Trimethoxy-6-methoxymethyl-tetrahydro-pyran-2-ol 
• 882-33-7 diphenyldisulfane 

Relevant articles and documents

Facile Diastereoseparation of Glycosyl Sulfoxides by Chiral Stationary Phase

Separation of the diastereomers of glycosyl sulfoxides differing in the sulfur chirality has been difficult. This article presents a fast and scalable method for their diastereoseparation using a chiral stationary phase. The usefulness of this method was

Sulfenate intermediates in the sulfoxide glycosylation reaction

The sulfoxide glycosylation reaction works remarkably well for many difficult glycosylations. We attribute this in part to the fact that an extremely reactive intermediate can be generated rapidly under mild conditions at low temperature. We find that ano