62983-70-4

Usage

Uses

Used in Pharmaceutical Synthesis:
DI-BETA-D-XYLOPYRANOSYLAMINE is used as a building block for the synthesis of various pharmaceuticals and natural products. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, DI-BETA-D-XYLOPYRANOSYLAMINE is used as a chiral auxiliary for the synthesis of complex molecules. Its ability to influence the stereochemistry of reactions makes it a useful tool in the creation of enantiomerically pure compounds.
Used in the Preparation of Glycosylated Compounds:
DI-BETA-D-XYLOPYRANOSYLAMINE is used as a starting material for the preparation of glycosylated compounds. These compounds have a wide range of applications, including in the development of new drugs, the modification of biologically active molecules, and the study of carbohydrate chemistry.
Used in Anti-inflammatory and Immunomodulatory Research:
DI-BETA-D-XYLOPYRANOSYLAMINE has been studied for its potential anti-inflammatory and immunomodulatory properties. This research could lead to the development of new treatments for inflammatory diseases and conditions where the immune system plays a significant role.

InChI:InChI=1/C10H19NO8/c12-3-1-18-9(7(16)5(3)14)11-10-8(17)6(15)4(13)2-19-10/h3-17H,1-2H2/t3-,4-,5+,6+,7-,8-,9-,10-/m1/s1

Upstream product

• 109-86-4 2-methoxy-ethanol 
• 67-56-1 methanol 
• 108-95-2 phenol 
• 30595-13-2 β-D-xylopyranosylamine 
• 114244-99-4 (2,3,4-tri-O-acetyl-α-D-xylopyranosyl)(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)amine 
• 114298-55-4 bis(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)amine 

Relevant academic research and scientific papers

STRUCTURE AND REARRANGEMENT REACTIONS OF SOME DIGLYCOSYLAMINES

Di-β-D-glucopyranosylamine (2) was prepared by transglycosylation from β-D-glucopyranosylamine.O-Acetylation of 2 led to partial anomerization and the formation of the expected octa-O-acetyl β,β derivative and its α,β anomer in the ratio 1:2,4.Similarly, transglycosylation of β-D-xylopyranosylamine afforded di-β-D-xylopyranosylamine (7).As with 2, the O-acetylation of 7 led to partial anomerization and formation of the hexa-O-acetyl α,β anomer of 7, as well as the expected β,β O-acetylated derivative.O-Deacetylation with ammonia in methanol of (2,3,4-tri-O-acetyl-α-D-xylopyranosyl)(2,3,4-tri-O-acetyl- β-D-xylopyranosyl)amine (7) led to recovery of the β,β-linked starting material.These rearrangement reactions are interpreted in terms of unfavorable nonbonded interactions which modify the thermodynamic equilibrium of the diglycosylamines.