2,4,7,8,9-Penta-O-acetyl-N-acetylneuraminic Acid Methyl Ester

≥98%

Reagent Code: #103673
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CAS Number 73208-82-9

science Other reagents with same CAS 73208-82-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 533.48 g/mol
Formula C₂₂H₃₁NO₁₄
thermostat Physical Properties
Melting Point 157℃
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily utilized in biochemical research, particularly in the study of sialic acids and their derivatives. It serves as a key intermediate in the synthesis of more complex sialic acid analogs, which are essential for investigating cell surface interactions, glycoprotein functions, and carbohydrate-mediated processes. Its acetylated form enhances stability, making it suitable for various chemical modifications and enzymatic studies. Additionally, it is employed in the development of glycoconjugates and glycomimetics, which have potential applications in drug discovery, vaccine development, and diagnostics targeting diseases involving sialic acid metabolism.

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

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,960.00
inventory 5g
10-20 days ฿29,800.00
inventory 1g
10-20 days ฿8,990.00

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2,4,7,8,9-Penta-O-acetyl-N-acetylneuraminic Acid Methyl Ester
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This compound is primarily utilized in biochemical research, particularly in the study of sialic acids and their derivatives. It serves as a key intermediate in the synthesis of more complex sialic acid analogs, which are essential for investigating cell surface interactions, glycoprotein functions, and carbohydrate-mediated processes. Its acetylated form enhances stability, making it suitable for various chemical modifications and enzymatic studies. Additionally, it is employed in the development of gly

This compound is primarily utilized in biochemical research, particularly in the study of sialic acids and their derivatives. It serves as a key intermediate in the synthesis of more complex sialic acid analogs, which are essential for investigating cell surface interactions, glycoprotein functions, and carbohydrate-mediated processes. Its acetylated form enhances stability, making it suitable for various chemical modifications and enzymatic studies. Additionally, it is employed in the development of glycoconjugates and glycomimetics, which have potential applications in drug discovery, vaccine development, and diagnostics targeting diseases involving sialic acid metabolism.

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