113842-46-9

Basic information

• Product Name: O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-1,6-anhydro-2,3-di-O-benzyl-β-D-glucopyranose
• Synonyms: O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-1,6-anhydro-2,3-di-O-benzyl-β-D-glucopyranose
• CAS NO: 113842-46-9
• Molecular Weight: 816.945
• Mol File: 113842-46-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-1,6-anhydro-2,3-di-O-benzyl-β-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-1,6-anhydro-2,3-di-O-benzyl-β-D-glucopyranose(113842-46-9)
• EPA Substance Registry System: O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-1,6-anhydro-2,3-di-O-benzyl-β-D-glucopyranose(113842-46-9)

Safety Data

• Hazardous Substances Data: 113842-46-9(Hazardous Substances Data)

Upstream product

• 113879-86-0 allyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 113842-86-7 O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranosyl fluoride 
• 113842-92-5 O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranosyl chloride 
• 85395-84-2 1,6-anhydro-2,3,2',3'-tetra-O-benzyl-4',6'-O-benzylidene-β-maltose 
• 113842-60-7 1,6-anhydro-2,2',3,3',6'-penta-O-benzyl-β-maltose 
• 108-24-7 acetic anhydride 

Downstream Products

• 86461-99-6 (2R,3R,4S,5R,6R)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-((1R,2R,3R,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-tetrahydro-pyran-3-ol 
• 192809-73-7 Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-((2R,3R,4S,5R)-4,5-bis-benzyloxy-6-methylsulfanyl-2-phenylcarbamoyloxymethyl-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester 
• 2672-63-1 1,6-anhydromaltose 

Relevant articles and documents

The Stereoselective Synthesis of Cyclomaltopentaose. A Novel Cyclodextrin Homologue with D.P. Five.

A key intermediate 15 was prepared via successive glycosidations of 1,6-anhydro maltose derivative 8 with glycosyl donors 6 and then with 11, cyclized under a diluted condition, and deprotected to give the title compound.Every glycosidation, including the