1,2:5,6-Di-O-isopropylidene-α-D-allofuranose
98%
Reagent
Code: #58042
Alias
1,2:5,6-Di-O-isopropylidene-α-D-allofuranose
1,2:5,6-Diisopropylidene-α-D-isofuranose
CAS Number
2595-05-3
blur_circular Chemical Specifications
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Molecular Information
Weight
260.28 g/mol
Formula
C₁₂H₂₀O₆
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Registry Numbers
MDL Number
MFCD00135634
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Physical Properties
Melting Point
73-76 °C(lit.)
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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 |
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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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