55682-49-0

Usage

Uses

Used in Organic Synthesis:
1,6-di-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranose is used as a synthetic intermediate for the preparation of various complex organic molecules, leveraging its unique structure and reactivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1,6-di-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranose is used as a building block for the development of new therapeutic agents, due to its ability to selectively interact with specific biological molecules.
Used in Biochemistry:
1,6-di-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranose serves as a valuable tool in biochemistry for understanding and manipulating biological processes, given its potential to be used as a substrate for various enzymatic reactions.

Upstream product

• 108-24-7 acetic anhydride 
• 55682-48-9 1,6-anhydro-2-azido-3,4-di-O-benzyl-2-deoxy-D-glucopyranose 
• 604-68-2 α-D-glucopyranose peracetylate 
• 67546-20-7 1,6-anhydro-2-azido-2-deoxy-β-D-glucopyranose 
• 139437-39-1 1,6-anhydro-2-deoxy-2-iodo-β-D-glucopyranose 
• 2873-29-2 D-glucal triacetate 
• 492-62-6 alpha-D-glucopyranose 

Downstream Products

• 79705-43-4 3-O-(2-Acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-glucopyranosyl)-1,6-anhydro-2,4-di-O-benzyl-β-D-galactopyranose 
• 79705-46-7 3-O-(2-Acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-glucopyranosyl)-1,6-di-O-acetyl-2,4-di-O-benzyl-β-D-galactopyranose 
• 79705-45-6 3-O-(2-Acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-glucopyranosyl)-1,6-di-O-acetyl-2,4-di-O-benzyl-α-D-galactopyranose 
• 55682-50-3 6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl bromide 

Relevant academic research and scientific papers

PROCESS FOR PREPARING HEPARINOIDS AND INTERMEDIATES USEFUL IN THE SYNTHESIS THEREOF

Processes are disclosed for the synthesis of the Factor Xa anticoagulant fondaparinux and related compounds. Protected pentasaccharide intermediates and efficient and scalable processes for the industrial scale production of fondaparinux sodium by conversion of the protected pentasaccharide intermediates via a sequence of deprotection and sulfonation reactions are provided.

A synthetic approach to aromatic aminoglycoside as a neamine mimic

This paper describes the synthetic approach to an aromatic a-glycoside as a mimic of neamine, which is a common core structure of some aminoglycoside antibiotics. We achieved the synthesis of the protected precursor of the neamine mimic, 4-(2,6-diamino-2,

OLIGOSACCHARIDE COMPOUNDS FOR USE IN MOBILISING STEM CELLS

A compound of the following formula or a salt, solvate or formula (I) and a pharmaceutical composition containing said compound. It concerns also its use in the treatment of cancer and/or of pathological angiogenesis and/or in promoting the mobilisation of stem cells, in particular hematopoietic stem cells.