(R)-N-Boc-2,2-dimethyl-4-vinyloxazolidine
95%
- Product Code: 37749
CAS:
115378-31-9
| Molecular Weight: | 227.3000 g./mol | Molecular Formula: | C₁₂H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18074306 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is widely utilized in organic synthesis as a chiral building block, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure, featuring a protected amine group (Boc) and a vinyl group, makes it valuable for asymmetric synthesis and stereoselective reactions. It is often employed in the synthesis of complex natural products and chiral intermediates, where the oxazolidine ring serves as a key scaffold for introducing stereochemistry. The vinyl group allows for further functionalization through reactions such as cross-coupling or polymerization, making it versatile in medicinal chemistry and materials science. Additionally, its stability under various reaction conditions makes it a preferred choice for multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,156.00 |
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(R)-N-Boc-2,2-dimethyl-4-vinyloxazolidine
This compound is widely utilized in organic synthesis as a chiral building block, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure, featuring a protected amine group (Boc) and a vinyl group, makes it valuable for asymmetric synthesis and stereoselective reactions. It is often employed in the synthesis of complex natural products and chiral intermediates, where the oxazolidine ring serves as a key scaffold for introducing stereochemistry. The vinyl group allows for further functionalization through reactions such as cross-coupling or polymerization, making it versatile in medicinal chemistry and materials science. Additionally, its stability under various reaction conditions makes it a preferred choice for multi-step synthetic processes.
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