(3AR,6aR)-2,2-dimethyl-6-((trityloxy)methyl)-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one
95%
- Product Code: 70893
CAS:
88559-56-2
| Molecular Weight: | 426.50 g./mol | Molecular Formula: | C₂₈H₂₆O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD25977133 | |
| Melting Point: | 161.2-163.2 °C | Boiling Point: | 547.6±50.0 °C(Predicted) |
| Density: | 1.175±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the synthesis of nucleosides and nucleotides, which are essential components in the development of antiviral and anticancer drugs. The trityl group in the compound acts as a protective group for hydroxyl functionalities, enabling selective reactions during multi-step synthetic processes. Its application is crucial in the pharmaceutical industry for the production of modified nucleosides that exhibit enhanced therapeutic properties. Additionally, it is employed in research laboratories for the study of glycosylation reactions and the development of novel bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿54,720.00 |
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(3AR,6aR)-2,2-dimethyl-6-((trityloxy)methyl)-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one
This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the synthesis of nucleosides and nucleotides, which are essential components in the development of antiviral and anticancer drugs. The trityl group in the compound acts as a protective group for hydroxyl functionalities, enabling selective reactions during multi-step synthetic processes. Its application is crucial in the pharmaceutical industry for the production of modified nucleosides that exhibit enhanced therapeutic properties. Additionally, it is employed in research laboratories for the study of glycosylation reactions and the development of novel bioactive compounds.
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