56865-31-7

Usage

Uses

Used in Pharmaceutical Industry:
Methyl 4-O-[4,6-O-(phenylmethylene)-beta-D-galactopyranosyl]-beta-D-glucopyranoside is used as a pharmaceutical compound for its potential therapeutic applications. Its unique glycoside structure may offer specific binding properties or serve as a precursor in the synthesis of other bioactive molecules, contributing to the development of new drugs.
Used in Food Science:
In the food science industry, Methyl 4-O-[4,6-O-(phenylmethylene)-beta-D-galactopyranosyl]-beta-D-glucopyranoside may be utilized for its functional properties, such as enhancing the texture or stability of food products. Its complex carbohydrate structure could also play a role in the development of novel food additives or sweeteners.
Used in Carbohydrate Chemistry Research:
Methyl 4-O-[4,6-O-(phenylmethylene)-beta-D-galactopyranosyl]-beta-D-glucopyranoside serves as a subject of study in carbohydrate chemistry, where researchers explore its properties, reactivity, and potential uses in creating new compounds or understanding the fundamental chemistry of glycosides.

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 7216-69-5 methyl β-D-lactopyranoside 
• 3616-19-1 1',2',3',6',2,3,4,6-octa-O-acetyl-β-D-lactose 
• 30021-61-5 methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 
• 100-52-7 benzaldehyde 

Downstream Products

• 144368-52-5 methyl 4',6'-O-benzylidene-6-deoxy-6-iodo-β-lactoside 
• 144368-59-2 methyl 3'-O-phenoxythiocarbonyl-β-lactoside 
• 914772-34-2 methyl 2,3,6,2',3'-penta-O-benzyl-4',6'-O-benzylidene-β-lactoside 
• 69983-00-2 methyl 2,3-di-O-acetyl-4,6-O-beznzylidene-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of tetrasaccharides as possible metastatic inhibitors

The synthesis is reported of the possible metastatic inhibitors - methyl β-D-galactopyranosyl-(1 → 4)-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-(1 → 6)-β-D-galactopyranosyl-(1 → 4)-β-D-glucopyranoside (11) and methyl β-D-galactopyranosyl-(1 → 4)-(2-acetami

An efficient glycosylation reaction for the synthesis of asialo GM2 analogues

We investigated the coupling reaction of glycosyl donors N-trichloroethoxycarbonyl-galactosamine-O-trichloroacetimidate (2a) and N-p-nitrobenzyloxycarbonyl-galactosamine-O-trichloroacetimidate (2b) with the 4′-OH of lactose derivatives (3a-d) to synthesiz

Synthesis and biological evaluation of sialylmimetics as rotavirus inhibitors

Rotaviruses cause severe gastroenteritis in infants and are estimated to be responsible for over 600 000 deaths annually, primarily in developing countries. The development of potential inhibitors of this virus is therefore of great interest, particularly since the safety and efficacy of rotaviral vaccines has recently been questioned. This study describes the synthesis of a variety of compounds that can be considered as mimetics of N-acetylneuraminic acid thioglycosides and the subsequent in vitro biological evaluation of these sialylmimetics as inhibitors of rotaviral infection. Our results show that readily accessible carbohydrate-based compounds have the potential to act as inhibitors of rotaviral replication in vitro, presumably through inhibition of the rotaviral adhesion process.

Carbohydrate-derived Surfactents: Synthesis and Phase Behaviour of Methyl 4',6'-Di-O-alkyl-β-lactosides

In order to study the physical properties of lactose-derived surfactants, methyl 4',6'-di-O-hexyl-β-lactoside and methyl 4',6'-di-O-octyl-β-lactoside were prepared.The 4',6'-O-isopropylidene ketal was used as a temporary protecting group in the key interm