4-Methylphenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside

≥98%

Reagent Code: #103728
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CAS Number 28244-94-2

science Other reagents with same CAS 28244-94-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.49074 g/mol
Formula C₂₁H₂₆O₉S
badge Registry Numbers
MDL Number MFCD13182351
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This chemical is primarily utilized in carbohydrate chemistry research, particularly in the synthesis of complex glycoconjugates. It serves as a key intermediate in the preparation of thioglycosides, which are essential for constructing oligosaccharides and glycoproteins. The acetyl groups protect the hydroxyl functionalities, allowing selective deprotection and further modification. It is also employed in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Additionally, it is used in the study of enzymatic glycosylation processes, aiding in understanding biochemical pathways.

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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 1g
10-20 days ฿1,240.00
inventory 5g
10-20 days ฿5,440.00

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4-Methylphenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside
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This chemical is primarily utilized in carbohydrate chemistry research, particularly in the synthesis of complex glycoconjugates. It serves as a key intermediate in the preparation of thioglycosides, which are essential for constructing oligosaccharides and glycoproteins. The acetyl groups protect the hydroxyl functionalities, allowing selective deprotection and further modification. It is also employed in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Additionally, it is used in the study of enzymatic glycosylation processes, aiding in understanding biochemical pathways.
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