Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-β-D-galactopyranoside

≥98%

Reagent Code: #103988
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CAS Number 24404-53-3

science Other reagents with same CAS 24404-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 440.46 g/mol
Formula C₂₀H₂₄O₉S
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a crucial intermediate in the preparation of oligosaccharides, which are essential for studying carbohydrate-protein interactions. Its acetylated groups protect the hydroxyl functionalities during chemical reactions, allowing selective deprotection for further modifications. This makes it valuable in glycosylation reactions, where it acts as a glycosyl donor to form glycosidic bonds. Additionally, it is employed in the development of glycoconjugate vaccines and in research focused on understanding cell surface interactions and signaling pathways. Its stability and reactivity make it a preferred choice in carbohydrate chemistry and glycobiology research.

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

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,000.00
inventory 1g
10-20 days ฿2,570.00

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Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-β-D-galactopyranoside
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This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a crucial intermediate in the preparation of oligosaccharides, which are essential for studying carbohydrate-protein interactions. Its acetylated groups protect the hydroxyl functionalities during chemical reactions, allowing selective deprotection for further modifications. This makes it valuable in glycosylation reactions, where it acts as a glycosyl donor to form glycosidic bonds. Additionally,

This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a crucial intermediate in the preparation of oligosaccharides, which are essential for studying carbohydrate-protein interactions. Its acetylated groups protect the hydroxyl functionalities during chemical reactions, allowing selective deprotection for further modifications. This makes it valuable in glycosylation reactions, where it acts as a glycosyl donor to form glycosidic bonds. Additionally, it is employed in the development of glycoconjugate vaccines and in research focused on understanding cell surface interactions and signaling pathways. Its stability and reactivity make it a preferred choice in carbohydrate chemistry and glycobiology research.

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