949489-26-3

Basic information

• Product Name: p-tolyl 3-O-(p-methoxybenzyl)-1-thio-β-D-galactopyranoside
• Synonyms: p-tolyl 3-O-(p-methoxybenzyl)-1-thio-β-D-galactopyranoside
• CAS NO: 949489-26-3
• Molecular Weight: 406.5
• Mol File: 949489-26-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: p-tolyl 3-O-(p-methoxybenzyl)-1-thio-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-tolyl 3-O-(p-methoxybenzyl)-1-thio-β-D-galactopyranoside(949489-26-3)
• EPA Substance Registry System: p-tolyl 3-O-(p-methoxybenzyl)-1-thio-β-D-galactopyranoside(949489-26-3)

Safety Data

• Hazardous Substances Data: 949489-26-3(Hazardous Substances Data)

Upstream product

• 1152-39-2 p-methylphenyl-1-thio-β-D-galactopyranoside 
• 824-94-2 p-methoxybenzyl chloride 
• 28244-94-2 4-methylphenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-galactopyranoside 
• 106-45-6 para-thiocresol 
• 4163-60-4 β-D-galactose peracetate 
• 25878-60-8 D-galactose pentaacetate 

Downstream Products

• 949489-27-4 p-tolyl 2,4,6-tri-O-benzyl-3-O-(p-methoxybenzyl)-1-thio-β-D-galactopyranoside 
• 1447700-78-8 (2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(5-(benzyloxycarbonylamino)pentyloxy)-4-(4-methoxybenzyloxy)tetrahydro-2H-pyran-3,5-diyl diacetate 
• 1447700-80-2 benzyl N-benzyl-N-(5-((2R,3R,4S,5R,6R)-3,5-bis(benzyloxy)-6-(benzyloxymethyl)-4-hydroxytetrahydro-2H-pyran-2-yloxy)pentyl)carbamate 
• 1447700-79-9 benzyl N-benzyl-N-(5-((2R,3R,4S,5S,6R)-3,5-bis(benzyloxy)-6-(benzyloxymethyl)-4-(4-methoxybenzyloxy)tetrahydro-2H-pyran-2-yloxy)pentyl)carbamate 
• 949489-25-2 p-tolyl 2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 

Relevant articles and documents

COMPOSITIONS AND METHODS FOR THE TREATMENT OF BACTERIAL INFECTIONS

Compositions and methods for the treatment of bacterial infections include compounds containing dimers of cyclic heptapeptides conjugated to one or more monosaccharide or oligosaccharide moieties. In particular, compounds can be used in the treatment of bacterial infections caused by Gram-negative bacteria.

Structural establishment of polygalatenosides A and B by total synthesis

The first total synthesis of polygalatenosides A (1) and B (2), originally isolated from the traditional Chinese medicine and reported as antidepressant agents, is described here. Glycosylation between thiogalactosyl donors 6 and 7 and 1-deoxyglucosyl acc