259871-09-5

Basic information

• Product Name: benzyl O-(2',3',4'-tri-O-benzyl-α-D-galactopyranosyl)-(1->4)-2-O-benzoyl-6-O-benzyl-α-D-glucopyranoside-3',6'-succinate
• Synonyms: benzyl O-(2',3',4'-tri-O-benzyl-α-D-galactopyranosyl)-(1->4)-2-O-benzoyl-6-O-benzyl-α-D-glucopyranoside-3',6'-succinate
• CAS NO: 259871-09-5
• Molecular Weight: 979.09
• Mol File: 259871-09-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl O-(2',3',4'-tri-O-benzyl-α-D-galactopyranosyl)-(1->4)-2-O-benzoyl-6-O-benzyl-α-D-glucopyranoside-3',6'-succinate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl O-(2',3',4'-tri-O-benzyl-α-D-galactopyranosyl)-(1->4)-2-O-benzoyl-6-O-benzyl-α-D-glucopyranoside-3',6'-succinate(259871-09-5)
• EPA Substance Registry System: benzyl O-(2',3',4'-tri-O-benzyl-α-D-galactopyranosyl)-(1->4)-2-O-benzoyl-6-O-benzyl-α-D-glucopyranoside-3',6'-succinate(259871-09-5)

Safety Data

• Hazardous Substances Data: 259871-09-5(Hazardous Substances Data)

Upstream product

• 259871-05-1 phenyl 6-O-(2-O-benzoyl-1-O-benzyl-4,6-O-benzylidene-α-D-glucopyranos-3-yloxycarbonylpropanoyl)-2,3,4-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 259871-04-0 phenyl 2,3,4-tri-O-benzyl-6-O-succinoyl-1-thio-β-D-galactopyranoside 
• 259871-03-9 phenyl 2,3,4-tri-O-benzyl-1-thio-6-O-trityl-β-D-galactopyranoside 
• 220774-86-7 phenyl 1-thio-6-O-triphenylmethyl-β-D-galactopyranoside 
• 38184-12-2 phenyl 2,3,4-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 16758-34-2 1-thiophenyl-β-D-galactopyranoside 
• 259871-06-2 phenyl 6-O-(2-O-benzoyl-1,6-di-O-benzyl-α-D-glucopyranos-3-yloxycarbonylpropanoyl)-2,3,4-tri-O-benzyl-1-thio-β-D-galactopyranoside 

Relevant articles and documents

Prearranged glycosides. Part 8. Intramolecular α-galactosylation via succinoyl tethered glycosides

Benzyl protected phenyl 1-thio-galactopyranoside donors which were tethered by a succinoyl linker at their positions 2 and 6, respectively, to position 3 of a blocked benzyl glucopyranoside acceptor with a 4-OH group solely afforded the corresponding α-(1→4)-linked disaccharides upon intramolecular glycosylation. 4,6-Siloxane protected mannosides react with rearrangement of the siloxane group under similar conditions.