(3R,4R,5R)-5-(Acetoxymethyl)tetrahydrofuran-2,3,4-triyl triacetate

95%

Reagent Code: #97353
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CAS Number 28708-32-9

science Other reagents with same CAS 28708-32-9

blur_circular Chemical Specifications

thermostat Physical Properties
Boiling Point 385.6°C
inventory_2 Storage & Handling
Density 1.29g/cm3
Storage -20°C

description Product Description

This compound is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure serves as a key intermediate in the production of modified nucleosides, enabling the creation of molecules that can inhibit viral replication or target cancer cells. Additionally, it is employed in carbohydrate chemistry research to study glycosylation processes, which are essential for understanding biological interactions and developing therapeutic agents. Its acetylated groups make it a versatile building block for constructing complex sugar derivatives used in drug discovery and biochemical studies.

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Test Parameter Specification
Appearance Solid
Purity 94.5-100

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿7,160.00
inventory 25g
10-20 days ฿890.00
inventory 5g
10-20 days ฿320.00
inventory 100g
10-20 days ฿2,480.00

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(3R,4R,5R)-5-(Acetoxymethyl)tetrahydrofuran-2,3,4-triyl triacetate
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This compound is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure serves as a key intermediate in the production of modified nucleosides, enabling the creation of molecules that can inhibit viral replication or target cancer cells. Additionally, it is employed in carbohydrate chemistry research to study glycosylation processes, which are essential for understanding biological interactions and developing therapeuti

This compound is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure serves as a key intermediate in the production of modified nucleosides, enabling the creation of molecules that can inhibit viral replication or target cancer cells. Additionally, it is employed in carbohydrate chemistry research to study glycosylation processes, which are essential for understanding biological interactions and developing therapeutic agents. Its acetylated groups make it a versatile building block for constructing complex sugar derivatives used in drug discovery and biochemical studies.

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