77437-65-1

Basic information

• Product Name: O-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-(1->6)-O-(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-N-(benzyl-N-benzyloxycarbonyl-L-asparthyl)-β-D-glucopyranosylamine
• CAS NO: 77437-65-1
• Molecular Weight: 1744.05
• Mol File: 77437-65-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: O-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-(1->6)-O-(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-N-(benzyl-N-benzyloxycarbonyl-L-asparthyl)-β-D-glucopyranosylamine(CAS DataBase Reference)
• NIST Chemistry Reference: O-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-(1->6)-O-(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-N-(benzyl-N-benzyloxycarbonyl-L-asparthyl)-β-D-glucopyranosylamine(77437-65-1)
• EPA Substance Registry System: O-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)-(1->6)-O-(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-N-(benzyl-N-benzyloxycarbonyl-L-asparthyl)-β-D-glucopyranosylamine(77437-65-1)

Safety Data

• Hazardous Substances Data: 77437-65-1(Hazardous Substances Data)

Upstream product

• 4779-31-1 Z-Asp-OBn 
• 77437-63-9 (3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-[(2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxymethyl)-tetrahydro-pyran-2-yloxymethyl]-tetrahydro-pyran-2-ylamine 
• 127570-61-0 2,3,4-tri-O-benzyl-N-(benzyl N-benzyloxycarbonyl-L-β-aspartyl)-α-D-glucopyranosylamine 
• 95084-13-2 phenylthio-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1→6)-2,3,4-tri-O-benzyl-β-D-glucopyranoside 

Downstream Products

• 77437-53-7 O-(α-D-glucopyranosyl)-(1<*>6)-O-β-D-glucopyranosyl-(1<*>6)-N-(L-β-aspartyl)-α-D-glucopyranosylamine 

Relevant articles and documents

An Efficient and Stereocontrolled Synthesis of the Nephritogenoside Core Structure

An efficient and stereocontrolled synthesis of the core trisaccharide 2 of nephritogenic glycopeptide, nephritogenoside 1 is described.Key to our synthetic strategy was β-selective glycosylation without neighboring group participation. Key words: nephrito

Synthetic studies on nephritogenic glycosides. Synthesis of alpha-Glc-(1 goes to 6)-beta-Glc-(1 goes to 6)-alpha Glc-(1 goes to Asn).

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