1,2:5,6-Di-O-isopropylidene-α-D-allofuranose

98%

Reagent Code: #58042
label
Alias 1,2:5,6-Di-O-isopropylidene-α-D-allofuranose 1,2:5,6-Diisopropylidene-α-D-isofuranose
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CAS Number 2595-05-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.28 g/mol
Formula C₁₂H₂₀O₆
badge Registry Numbers
MDL Number MFCD00135634
thermostat Physical Properties
Melting Point 73-76 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

1,2:5,6-Di-O-isopropylidene-α-D-allofuranose is widely used as a key intermediate in organic synthesis, particularly in the production of complex carbohydrates and nucleosides. Its protective isopropylidene groups make it a valuable building block for creating selectively modified sugar molecules. It is also employed in the synthesis of glycosides, which are essential in developing pharmaceuticals and bioactive compounds. Additionally, this chemical plays a role in carbohydrate chemistry research, aiding in the study of sugar reactivity and stereochemistry. Its stability and versatility make it a preferred choice for constructing intricate molecular structures in medicinal chemistry and biochemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 74-77
Purity (GC) 98-100%
Specific Rotation (α20/D CHCl3) 35-38
Appearance White powder, crystals and/or chunks
Infrared Spectrum Conforms to Structure
Solubility in Toluene almost transparent

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿680.00
inventory 1g
10-20 days ฿280.00
inventory 25g
10-20 days ฿2,580.00
inventory 100g
10-20 days ฿9,350.00
1,2:5,6-Di-O-isopropylidene-α-D-allofuranose
1,2:5,6-Di-O-isopropylidene-α-D-allofuranose is widely used as a key intermediate in organic synthesis, particularly in the production of complex carbohydrates and nucleosides. Its protective isopropylidene groups make it a valuable building block for creating selectively modified sugar molecules. It is also employed in the synthesis of glycosides, which are essential in developing pharmaceuticals and bioactive compounds. Additionally, this chemical plays a role in carbohydrate chemistry research, aiding in the study of sugar reactivity and stereochemistry. Its stability and versatility make it a preferred choice for constructing intricate molecular structures in medicinal chemistry and biochemistry.
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