1,2:5,6-Di-O-isopropylidene-α-D-allofuranose
98%
- Product Code: 58042
Alias:
1,2:5,6-Di-O-isopropylidene-α-D-allofuranose
1,2:5,6-Diisopropylidene-α-D-isofuranose
CAS:
2595-05-3
| Molecular Weight: | 260.28 g./mol | Molecular Formula: | C₁₂H₂₀O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00135634 | |
| Melting Point: | 73-76 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
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.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 74 77? |
| PurityGC | 98 100% |
| SPECIFIC ROTATION A20DC1 CHCL3 | 35 38 |
| APPEARANCE | White powder, crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
| SOLUBILITY IN TOLUENE | almost transparency |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿280.00 |
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| 5.000 | 10-20 days | ฿680.00 |
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| 25.000 | 10-20 days | ฿2,580.00 |
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| 100.000 | 10-20 days | ฿9,350.00 |
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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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