85395-92-2

Basic information

• Product Name: 1,6-anhydro-4'-azido-2,3,2',3'-tetra-O-benzyl-4',6'-dideoxy-β-maltose
• Synonyms: 1,6-anhydro-4'-azido-2,3,2',3'-tetra-O-benzyl-4',6'-dideoxy-β-maltose
• CAS NO: 85395-92-2
• Molecular Weight: 693.797
• Mol File: 85395-92-2.mol

Chemical Properties

• CAS DataBase Reference: 1,6-anhydro-4'-azido-2,3,2',3'-tetra-O-benzyl-4',6'-dideoxy-β-maltose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-anhydro-4'-azido-2,3,2',3'-tetra-O-benzyl-4',6'-dideoxy-β-maltose(85395-92-2)
• EPA Substance Registry System: 1,6-anhydro-4'-azido-2,3,2',3'-tetra-O-benzyl-4',6'-dideoxy-β-maltose(85395-92-2)

Safety Data

• Hazardous Substances Data: 85395-92-2(Hazardous Substances Data)

Upstream product

• 85395-90-0 1,6-anhydro-2,3-di-O-benzyl-4-O-(2,3-di-O-benzyl-6-deoxy-α-D-galactopyranosyl)-β-D-glucopyranose 
• 85395-87-5 1,6-anhydro-2,3,2',3'-tetra-O-benzyl-6'-deoxy-β-maltose 
• 85395-84-2 1,6-anhydro-2,3,2',3'-tetra-O-benzyl-4',6'-O-benzylidene-β-maltose 
• 85395-88-6 1,6-anhydro-2,3,2',3'-tetra-O-benzyl-6'-deoxy-4'-O-(methylsulfonyl)-β-maltose 
• 85395-85-3 1,6-anhydro-2,3,2',3'-tetra-O-benzyl-β-maltose 
• 85395-86-4 1,6-anhydro-2,3-di-O-benzyl-4-O-(2,3-di-O-benzyl-6-O-deoxy-6-iodo-β-D-glucopyranosyl)-β-D-glucopyranose 
• 100-39-0 benzyl bromide 
• 56838-37-0 2,3,2',3'-tetra-O-acetyl-1,6-anhydro-4',6'-O-benzylidene-β-maltose 
• 85395-91-1 1,6-anhydro-2,3-di-O-benzyl-4-O-<2,3-di-O-benzyl-6-deoxy-4-O-(methylsulfonyl)-α-D-galactopyranosyl>-β-D-glucopyranose 
• 85395-89-7 1,6-anhydro-2,3-di-O-benzyl-4-O-(2,3-di-O-benzyl-4-chloro-4,6-dideoxy-α-D-galactopyranosyl)-β-D-glucopyranose 

Downstream Products

• 85395-93-3 4'-amino-1,6-anhydro-2,2',3,3'-tetra-O-benzyl-4',6'-dideoxy-β-maltose 

Relevant articles and documents

SYNTHESIS OF A 4'-AMINO-4',6'-DIDEOXYMALTOSE DERIVATIVE AS A SYNTHON OF AN α-D-GLUCOSIDASE INHIBITOR

4'-Amino-1,6-anhydro-2,3,2',3'-tetra-O-benzyl-4',6'-dideoxy-β-maltose, required as a synthon for the preparation of an α-D-glucosidase inhibitor constituted of a basic pseudotrisaccharide, was prepared from 1,6-anhydromaltose (2).Two pathways were examine