1,2,3-Tri-O-acetyl-5-deoxy-β-D-ribofuranose
97%
- Product Code: 96293
Alias:
1,2,3-Triacetoxy-5-deoxy-β-D-ribose
CAS:
62211-93-2
| Molecular Weight: | 260.24 g./mol | Molecular Formula: | C₁₁H₁₆O₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08458459 | |
| Melting Point: | 63-64°C | Boiling Point: | 315°C |
| Density: | 1.23 | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as an intermediate in the production of modified nucleosides, enabling the creation of molecules that can interfere with viral replication or cancer cell proliferation. Additionally, it is employed in carbohydrate chemistry research to study glycosylation reactions and to develop novel glycosides with potential therapeutic applications. Its acetyl groups provide protection during chemical transformations, ensuring selective reactions and enhancing the efficiency of synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿490.00 |
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| 25.000 | 10-20 days | ฿620.00 |
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| 100.000 | 10-20 days | ฿1,990.00 |
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| 500.000 | 10-20 days | ฿7,320.00 |
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1,2,3-Tri-O-acetyl-5-deoxy-β-D-ribofuranose
This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It serves as an intermediate in the production of modified nucleosides, enabling the creation of molecules that can interfere with viral replication or cancer cell proliferation. Additionally, it is employed in carbohydrate chemistry research to study glycosylation reactions and to develop novel glycosides with potential therapeutic applications. Its acetyl groups provide protection during chemical transformations, ensuring selective reactions and enhancing the efficiency of synthetic processes.
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