Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside

≥98%

Reagent Code: #103998
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CAS Number 108032-93-5

science Other reagents with same CAS 108032-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 440.46 g/mol
Formula C₂₀H₂₄O₉S
badge Registry Numbers
MDL Number MFCD01862644
thermostat Physical Properties
Melting Point 85°C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of mannose-containing oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. The acetyl groups protect the hydroxyl functionalities during synthetic procedures, allowing selective deprotection for further modifications. It is also employed in the development of glycoproteins and glycolipids, which have applications in vaccine development and drug delivery systems. Additionally, it plays a role in the creation of glycosidase inhibitors, which are potential therapeutic agents for treating metabolic disorders and viral infections.

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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 ฿4,400.00

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Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside
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This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of mannose-containing oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. The acetyl groups protect the hydroxyl functionalities during synthetic procedures, allowing selective deprotection for further modifications. It is also employed in the development of glycoproteins and glycolipids, which hav

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of mannose-containing oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. The acetyl groups protect the hydroxyl functionalities during synthetic procedures, allowing selective deprotection for further modifications. It is also employed in the development of glycoproteins and glycolipids, which have applications in vaccine development and drug delivery systems. Additionally, it plays a role in the creation of glycosidase inhibitors, which are potential therapeutic agents for treating metabolic disorders and viral infections.

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