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Usage

Uses

Used in Organic Synthesis:
4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is used as an intermediate in the synthesis of various complex organic compounds, particularly those involving carbohydrates and their derivatives. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is used as a key compound in the development of new drugs targeting various diseases. Its ability to form glycosidic bonds with other molecules makes it a valuable building block for the synthesis of glycoconjugates, which have potential therapeutic applications.
Used in Chemical Research:
4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is also utilized in chemical research as a model compound for studying the properties and reactivity of glycosidic bonds. This helps researchers understand the fundamental principles governing the formation and cleavage of these bonds, which is crucial for the development of new synthetic methods and applications.
Used in Material Science:
In the field of material science, 4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside can be used as a component in the development of novel materials with specific properties. Its ability to form hydrogen bonds and interact with other molecules can lead to the creation of materials with unique mechanical, thermal, or electrical properties.

Upstream product

• 93979-04-5 p-nitrophenyl 3-O-benzoyl-4,6-O-benzylidene-2-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-α-D-mannopyranoside 
• 14218-11-2 2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide 
• 2492-87-7 p-nitrophenyl β-D-mannopyranoside 
• 210281-95-1 β-D-mannopyranosyl fluoride 
• 10357-27-4 4-nitrophenyl-α-D-mannopyranoside 
• 439-03-2 2,3,4,6-tetra-O-acetyl-β-D-mannopyranosyl fluoride 
• 79580-52-2 p-nitrophenyl 3-O-benzoyl-4,6-di-O-benzylidene-α-D-mannopyranoside 

Relevant academic research and scientific papers

Creation of an α-mannosynthase from a broad glycosidase scaffold

α-Mannosides made easy: Mutation of a family-GH31 α-glucosidase that displays plasticity to alterations at the 2-OH position of donor substrates created an efficient α-mannoside-synthesizing biocatalyst. A simple fluoride donor reagent was used for the synthesis of a range of mono-α-mannosylated conjugates using the α-mannosynthase displaying low (unwanted) oligomerization activity. Copyright

A SIMPLE STRATEGY FOR CHANGING THE REGIOSELECTIVITY OF GLYCOSIDASE-CATALYSED FORMATION OF DISACCHARIDES

The regioselectivity of glycosidase-catalysed formation of disaccharides can be changed by using α- or β-glycosyl acceptors with various aglycons.The preponderant formation of other than (1->6) linkages can be effected with glycosidases which normally give (1->6) linkages.Thus, an α-D-galactosidase can be induced to catalyse the formation mainly of α-(1->2)-, α-(1->3)-, or α-(1->6)-linked digalctosides.Both the structure of the aglycon and the configuration of the glycosidic linkage can have a pronounced influence on the regioselectivity of disaccharide formation.Enzymic syntheses, in yields of 20-30percent, are described of α-D-Galp-(1->3)-α-D-Galp-OMe, β-D-Galp-(1->3)-β-D-Galp-OMe, β-D-Galp-(1->6)-α-D-Galp-OMe, α-D-Manp-(1->2)-α-D-Manp-OMe, α-D-Manp-(1->6)-α-D-Manp-OMe, α-D-Galp-(1->2)-α-D-Galp-OPhNO2-o, α-D-Galp-(1->3)-α-D-Galp-OPhNO2-p, α-D-Manp-(1->2)-α-D-Manp-OPhNO2-p, and α-D-Manp-(1->2)-α-D-Manp-(1->2)-α-D-Manp-OMe.Soluble and immobilised enzymes have been used.

p-NITROPHENYL 2-, AND 3-O-α-D-MANNOPYRANOSYL-α-D-MANNOPYRANOSIDE

p-Nitrophenyl 3- and 2-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranoside were each condensed with 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl bromide, and the products were deprotected, to yield, respectively, p-nitrophenyl 2- and 3-O-mannopyranosyl-α-D-mann