1,2,3-Tri-O-acetyl-5-deoxy-β-D-ribofuranose

97%

Reagent Code: #96293
label
Alias 1,2,3-Triacetoxy-5-deoxy-β-D-ribose
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CAS Number 62211-93-2

science Other reagents with same CAS 62211-93-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.24 g/mol
Formula C₁₁H₁₆O₇
badge Registry Numbers
MDL Number MFCD08458459
thermostat Physical Properties
Melting Point 63-64°C
Boiling Point 315°C
inventory_2 Storage & Handling
Density 1.23
Storage 2~8°C

description Product Description

This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as an intermediate in the production of modified nucleosides, enabling the creation of molecules that can interfere with viral replication or cancer cell proliferation. Additionally, it is employed in carbohydrate chemistry research to study glycosylation reactions and to develop novel glycosides with potential therapeutic applications. Its acetyl groups provide protection during chemical transformations, ensuring selective reactions and enhancing the efficiency of synthetic processes.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿490.00
inventory 500g
10-20 days ฿7,320.00
inventory 25g
10-20 days ฿620.00
inventory 100g
10-20 days ฿1,990.00

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1,2,3-Tri-O-acetyl-5-deoxy-β-D-ribofuranose
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This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as an intermediate in the production of modified nucleosides, enabling the creation of molecules that can interfere with viral replication or cancer cell proliferation. Additionally, it is employed in carbohydrate chemistry research to study glycosylation reactions and to develop novel glycosides with potential therapeutic applications. Its acetyl g

This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as an intermediate in the production of modified nucleosides, enabling the creation of molecules that can interfere with viral replication or cancer cell proliferation. Additionally, it is employed in carbohydrate chemistry research to study glycosylation reactions and to develop novel glycosides with potential therapeutic applications. Its acetyl groups provide protection during chemical transformations, ensuring selective reactions and enhancing the efficiency of synthetic processes.

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