444808-94-0

Basic information

• Product Name: 1,3-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-β-D-galactopyranosyl)-glycerol
• Synonyms: 1,3-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-β-D-galactopyranosyl)-glycerol
• CAS NO: 444808-94-0
• Molecular Weight: 704.86
• Mol File: 444808-94-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-β-D-galactopyranosyl)-glycerol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-β-D-galactopyranosyl)-glycerol(444808-94-0)
• EPA Substance Registry System: 1,3-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-β-D-galactopyranosyl)-glycerol(444808-94-0)

Safety Data

• Hazardous Substances Data: 444808-94-0(Hazardous Substances Data)

Upstream product

• 444808-92-8 1,3-di-O-benzyl-2-O-(6-O-trityl-β-D-galactopyranosyl)glycerol 
• 444808-91-7 1,3-di-O-benzyl-2-O-β-D-(galactopyranosyl)-glycerol 
• 6972-79-8 dibenzyl glycerol 
• 444808-93-9 1,3-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-trityl-β-D-galactopyranosyl)glycerol 

Downstream Products

• 444808-98-4 1,3-di-O-benzyl-2-O-[(6Z)-2,3,4-tri-O-benzyl-6,7,8,9,10,11,12,13-octadeoxy-β-D-galacto-tridec-6-enopyranosyl]glycerol 
• 444808-97-3 (2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-tetrahydro-pyran-2-carbaldehyde 
• 444808-95-1 1,3-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-hexyl-β-D-galactopyranosyl)glycerol 

Relevant articles and documents

Synthesis of isosteric analogues of acylglycosylglycerols active as chemoprevention agents

Monoacylated glycosylglycerols are known anti-tumor promoters: in order to study the role of the ester function in the modulation of their activity, we synthesized several analogues in which the acyloxy moiety was substituted with isosteric chains linked to the glycosylglycerol skeleton through an ether or a ketone functionality or simply by a C-C bond. Depending on the position of the chain, the key steps in the synthesis were either the coupling of suitable chiral synthons with the sugar, with complete stereocontrol over the anomeric configuration, or regioselective elaboration at position 6 of the sugar. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.