((3AS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)(morpholino)methanone
98%
- Product Code: 36070
CAS:
1103738-19-7
| Molecular Weight: | 273.28 g./mol | Molecular Formula: | C₁₂H₁₉NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 479.3±45.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure, featuring a morpholino group and a tetrahydrofuro[1,3]dioxolane moiety, makes it a valuable intermediate in organic synthesis. The compound is often employed in the preparation of modified nucleosides, which can inhibit viral replication or interfere with cancer cell proliferation. Additionally, it serves as a building block in the creation of prodrugs, enhancing the bioavailability and stability of therapeutic agents. Its applications extend to research in medicinal chemistry, where it aids in the design of novel compounds with potential pharmacological activities.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿300.00 |
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| 0.250 | 10-20 days | ฿650.00 |
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| 1.000 | 10-20 days | ฿2,550.00 |
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((3AS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)(morpholino)methanone
This chemical is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure, featuring a morpholino group and a tetrahydrofuro[1,3]dioxolane moiety, makes it a valuable intermediate in organic synthesis. The compound is often employed in the preparation of modified nucleosides, which can inhibit viral replication or interfere with cancer cell proliferation. Additionally, it serves as a building block in the creation of prodrugs, enhancing the bioavailability and stability of therapeutic agents. Its applications extend to research in medicinal chemistry, where it aids in the design of novel compounds with potential pharmacological activities.
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