2-Acetamido-4-fluoro-1,3,6-tri-O-acetyl-2,4-dideoxy-D-glucopyranose

≥98%

Reagent Code: #103685
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CAS Number 116049-57-1

science Other reagents with same CAS 116049-57-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 349.31 g/mol
Formula C₁₄H₂₀FNO₈
inventory_2 Storage & Handling
Density 1.30 g/cm3(Predicted)
Storage -20°C

description Product Description

This chemical is primarily utilized in the synthesis of modified sugars and glycosides, which are crucial in the development of pharmaceuticals and biochemical research. It serves as an intermediate in the production of nucleoside analogs, which are important in antiviral and anticancer drug development. The compound's unique structure allows for the introduction of fluorine atoms into sugar molecules, enhancing their biological activity and stability. Additionally, it is used in glycosylation reactions to study enzyme mechanisms and to create novel glycoconjugates for therapeutic and diagnostic applications. Its role in advancing carbohydrate chemistry makes it valuable in both academic and industrial settings.

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Test Parameter Specification
Appearance White to off-white solid to semi-solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿40,230.00
inventory 5mg
10-20 days ฿26,980.00

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2-Acetamido-4-fluoro-1,3,6-tri-O-acetyl-2,4-dideoxy-D-glucopyranose
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This chemical is primarily utilized in the synthesis of modified sugars and glycosides, which are crucial in the development of pharmaceuticals and biochemical research. It serves as an intermediate in the production of nucleoside analogs, which are important in antiviral and anticancer drug development. The compound's unique structure allows for the introduction of fluorine atoms into sugar molecules, enhancing their biological activity and stability. Additionally, it is used in glycosylation reactions

This chemical is primarily utilized in the synthesis of modified sugars and glycosides, which are crucial in the development of pharmaceuticals and biochemical research. It serves as an intermediate in the production of nucleoside analogs, which are important in antiviral and anticancer drug development. The compound's unique structure allows for the introduction of fluorine atoms into sugar molecules, enhancing their biological activity and stability. Additionally, it is used in glycosylation reactions to study enzyme mechanisms and to create novel glycoconjugates for therapeutic and diagnostic applications. Its role in advancing carbohydrate chemistry makes it valuable in both academic and industrial settings.

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