2,3,4,6-Tetraacetyl-D-glucose

96%

Reagent Code: #103667
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CAS Number 10343-06-3

science Other reagents with same CAS 10343-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.3 g/mol
Formula C₁₄H₂₀O₁₀
badge Registry Numbers
MDL Number MFCD00061634
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

2,3,4,6-Tetraacetyl-D-glucose is widely used as an intermediate in organic synthesis, particularly in the production of complex carbohydrates and glycoconjugates. It serves as a protected form of glucose, allowing selective reactions at specific hydroxyl groups without unwanted side reactions. This compound is essential in the synthesis of glycosides, oligosaccharides, and other sugar derivatives, which are crucial in developing pharmaceuticals, including antiviral and anticancer drugs. Additionally, it is employed in the preparation of glycosyl donors for glycosylation reactions, a key step in carbohydrate chemistry. Its acetyl groups provide stability and control during synthetic processes, making it a valuable tool in both academic research and industrial applications.

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Test Parameter Specification
Appearance White Solid
Purity (%) 95.5-100
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,030.00
inventory 1g
10-20 days ฿2,780.00
inventory 250mg
10-20 days ฿1,390.00

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2,3,4,6-Tetraacetyl-D-glucose
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2,3,4,6-Tetraacetyl-D-glucose is widely used as an intermediate in organic synthesis, particularly in the production of complex carbohydrates and glycoconjugates. It serves as a protected form of glucose, allowing selective reactions at specific hydroxyl groups without unwanted side reactions. This compound is essential in the synthesis of glycosides, oligosaccharides, and other sugar derivatives, which are crucial in developing pharmaceuticals, including antiviral and anticancer drugs. Additionally, it

2,3,4,6-Tetraacetyl-D-glucose is widely used as an intermediate in organic synthesis, particularly in the production of complex carbohydrates and glycoconjugates. It serves as a protected form of glucose, allowing selective reactions at specific hydroxyl groups without unwanted side reactions. This compound is essential in the synthesis of glycosides, oligosaccharides, and other sugar derivatives, which are crucial in developing pharmaceuticals, including antiviral and anticancer drugs. Additionally, it is employed in the preparation of glycosyl donors for glycosylation reactions, a key step in carbohydrate chemistry. Its acetyl groups provide stability and control during synthetic processes, making it a valuable tool in both academic research and industrial applications.

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