100605-69-4

Usage

General Description

Allyl 2,3-di-O-benzyl-α-D-galactopyranoside is a chemical compound with the molecular formula C25H28O6. It is a benzyl-protected derivative of α-D-galactopyranoside, which is a type of sugar. allyl 2,3-di-O-benzyl-α-D-galactopyranoside is commonly used in organic chemistry and biochemistry research as a reagent and building block for the synthesis of various glycosides and other carbohydrate derivatives. It is also used in the pharmaceutical industry as a precursor for the production of potential drug candidates. The allyl group in the structure provides a site for further functionalization and manipulation of the molecule, making it a versatile and useful compound in chemical synthesis.

Upstream product

• 2595-07-5 allyl D-galactopyranoside 
• 10343-15-4 allyl 2,3,4,6-tetra-O-acetyl-D-galactopyranoside 
• 4163-60-4 β-D-galactose peracetate 
• 10257-28-0 D-Galactose 
• 100-39-0 benzyl bromide 
• 100759-10-2 allyl 4,6-di-O-benzylidene-α-D-galactopyranoside 
• 100759-11-3 allyl 2,3-di-O-benzyl-4,6-di-O-benzylidene-α-D-galactopyranoside 

Downstream Products

• 100605-70-7 allyl 2,3-di-O-benzyl-6-O-p-tosyl-α-D-galactopyranoside 
• 100605-71-8 Allyl-4-O-acetyl-2,3-di-O-benzyl-6-O-tosyl-α-D-galactopyranosid 
• 100605-72-9 Allyl-2,3-di-O-benzyl-6-desoxy-α-D-galactopyranosid 

Relevant academic research and scientific papers

Synthesis of oligosaccharide fragments of the rhamnogalacturonan of Nerium indicum

Three trisaccharides, one pentasaccharide, and one heptasaccharide, namely α-D-GalA-(1→2)-α-L-Rha-(1→4)-β-D-GalA-OC 3H7 (1), α-L-Rha-(1→4)-α-D-GalA- (1→4)-β-D-GalA-OC3H7 (2), α-D-GalA- (1→4)-α-DGalA-(1→2)-α-L-Rh

In situ activating glycosylation of 6-deoxysugars: Synthesis of O- α-D- fucosyl(1→4)-O-α-D-fucosyl-(1→4)-O-α-D-quinovosyl-(1→4)-D-quinovose

The linear tetrasaccharide, α-D-fucopyranosyl-(1→4)-a-D-fucopyranosyl- (1→4)-α-D-quinovopyranosyl-(1→4)-D-quinovopyranose, the sugar cluster of asterosaponin A from the starfish, Asterias amurensis, was synthesized in a convergent manner. We employed an i

Syntheses of Methyl 4-O-(β-D-Curacosyl)-α-D-curamicoside, the Glycoside of the Disaccharide Moiety E-F of Flambamycin and Isomers

By application of the tetraisopropyldisiloxy function a five-step synthesis of the selectively protected 2,6-di-O-methylmannopyranoside 5a is achieved.Additionally several steps are used to transfer the galactopyranoside 7 into the α-bromide of 4-O-methyl