(S)-(-)-3-(tert-Butoxycarbonyl)-4-formyl-2,2-dimethyl-1,3-oxazolidine
≥95%
- Product Code: 62516
CAS:
102308-32-7
| Molecular Weight: | 229.28 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00209557 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is widely used in organic synthesis as a chiral auxiliary and protecting group, particularly in the preparation of enantiomerically pure compounds. Its structure allows for the selective protection of amino groups during complex multi-step reactions, ensuring the desired stereochemistry is maintained. It is especially valuable in the synthesis of pharmaceuticals, where precise chiral control is critical for drug efficacy and safety. Additionally, it is employed in peptide chemistry to protect amino acids during coupling reactions, preventing unwanted side reactions. Its stability under various reaction conditions makes it a versatile tool in asymmetric synthesis and the development of biologically active molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless - Pale yellow Liquid |
| PURITY | 94.5-100 |
| SPECIFIC GRAVITY 2020 | 1.0570-1.0600 |
| Refractive index n20D | 1.4450-1.4470 |
| Specific rotation a20Dc1 CHCl3 | -98--85 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿950.00 |
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| 1.000 | 10-20 days | ฿2,940.00 |
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| 5.000 | 10-20 days | ฿9,750.00 |
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| 25.000 | 10-20 days | ฿31,150.00 |
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(S)-(-)-3-(tert-Butoxycarbonyl)-4-formyl-2,2-dimethyl-1,3-oxazolidine
This compound is widely used in organic synthesis as a chiral auxiliary and protecting group, particularly in the preparation of enantiomerically pure compounds. Its structure allows for the selective protection of amino groups during complex multi-step reactions, ensuring the desired stereochemistry is maintained. It is especially valuable in the synthesis of pharmaceuticals, where precise chiral control is critical for drug efficacy and safety. Additionally, it is employed in peptide chemistry to protect amino acids during coupling reactions, preventing unwanted side reactions. Its stability under various reaction conditions makes it a versatile tool in asymmetric synthesis and the development of biologically active molecules.
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