2-Deoxy-2-fluoro-1,3,5-tri-O-benzoyl-D-ribofuranose

95%

Reagent Code: #97158
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Alias Clorabine intermediate
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CAS Number 97614-43-2

science Other reagents with same CAS 97614-43-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.44 g/mol
Formula C₂₆H₂₁FO₇
badge Registry Numbers
MDL Number MFCD00083339
thermostat Physical Properties
Melting Point 74-77°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is primarily utilized in the synthesis of nucleoside analogs, which are critical in the development of antiviral and anticancer drugs. Its fluorinated structure enhances the stability and bioavailability of these analogs, making it a valuable intermediate in medicinal chemistry. Additionally, it is employed in the preparation of modified sugars used in biochemical research to study enzyme mechanisms and carbohydrate metabolism. The benzoyl groups provide protection during synthetic processes, ensuring selective reactions and high yields in complex organic syntheses.

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Test Parameter Specification
Purity (HPLC) 94.5-100%
Appearance white-yellow powder
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,180.00
inventory 25g
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿320.00

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2-Deoxy-2-fluoro-1,3,5-tri-O-benzoyl-D-ribofuranose
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This compound is primarily utilized in the synthesis of nucleoside analogs, which are critical in the development of antiviral and anticancer drugs. Its fluorinated structure enhances the stability and bioavailability of these analogs, making it a valuable intermediate in medicinal chemistry. Additionally, it is employed in the preparation of modified sugars used in biochemical research to study enzyme mechanisms and carbohydrate metabolism. The benzoyl groups provide protection during synthetic processe

This compound is primarily utilized in the synthesis of nucleoside analogs, which are critical in the development of antiviral and anticancer drugs. Its fluorinated structure enhances the stability and bioavailability of these analogs, making it a valuable intermediate in medicinal chemistry. Additionally, it is employed in the preparation of modified sugars used in biochemical research to study enzyme mechanisms and carbohydrate metabolism. The benzoyl groups provide protection during synthetic processes, ensuring selective reactions and high yields in complex organic syntheses.

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