(R)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane
97%
- Product Code: 71047
CAS:
14347-83-2
| Molecular Weight: | 222.28 g./mol | Molecular Formula: | C₁₃H₁₈O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066533 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.05g/ml | Storage Condition: | room temperature, in an inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral building block. It serves as a key intermediate in the production of enantiomerically pure pharmaceuticals, particularly in the synthesis of complex molecules where stereochemistry is critical. Its structure, featuring a benzyloxymethyl group, makes it useful for protecting and deprotecting functional groups during multi-step synthetic processes. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) where the specific (R)-configuration is required for biological activity. Its stability and ease of manipulation under various reaction conditions make it a valuable tool in asymmetric synthesis and medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £26.46 |
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(R)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane
This compound is primarily utilized in organic synthesis as a chiral building block. It serves as a key intermediate in the production of enantiomerically pure pharmaceuticals, particularly in the synthesis of complex molecules where stereochemistry is critical. Its structure, featuring a benzyloxymethyl group, makes it useful for protecting and deprotecting functional groups during multi-step synthetic processes. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) where the specific (R)-configuration is required for biological activity. Its stability and ease of manipulation under various reaction conditions make it a valuable tool in asymmetric synthesis and medicinal chemistry research.
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