Ethyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-thioglucopyranoside

≥98%

Reagent Code: #103882
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CAS Number 99409-32-2

science Other reagents with same CAS 99409-32-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 479.50 g/mol
Formula C₂₂H₂₅NO₉S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for constructing glycosidic bonds in oligosaccharides. Its protective groups, such as acetyl and phthalimido, enhance stability and selectivity during chemical reactions, making it valuable in carbohydrate chemistry research. Additionally, it is employed in the development of bioactive molecules, including potential drug candidates targeting bacterial infections, as it mimics sugar moieties crucial for microbial adhesion and recognition. Its thioglycoside functionality allows for versatile activation strategies in glycosylation reactions, facilitating the creation of diverse glycan structures for biological studies.

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Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿830.00
inventory 1g
10-20 days ฿2,130.00

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Ethyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-thioglucopyranoside
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This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for constructing glycosidic bonds in oligosaccharides. Its protective groups, such as acetyl and phthalimido, enhance stability and selectivity during chemical reactions, making it valuable in carbohydrate chemistry research. Additionally, it is employed in the development of bioactive molecules, including potential d

This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for constructing glycosidic bonds in oligosaccharides. Its protective groups, such as acetyl and phthalimido, enhance stability and selectivity during chemical reactions, making it valuable in carbohydrate chemistry research. Additionally, it is employed in the development of bioactive molecules, including potential drug candidates targeting bacterial infections, as it mimics sugar moieties crucial for microbial adhesion and recognition. Its thioglycoside functionality allows for versatile activation strategies in glycosylation reactions, facilitating the creation of diverse glycan structures for biological studies.

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