(R)-3-(tert-Butoxycarbonyl)-2,2-dimethyloxazolidine-4-carboxylic acid
98%
- Product Code: 55423
CAS:
660852-86-8
| Molecular Weight: | 245.2700 g./mol | Molecular Formula: | C₁₁H₁₉NO₅ |
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| EC Number: | MDL Number: | MFCD06203312 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a chiral auxiliary or building block in asymmetric synthesis. It plays a crucial role in the preparation of enantiomerically pure compounds, particularly in pharmaceutical research and development. Its structure is valuable for controlling stereochemistry during the synthesis of complex molecules, such as active pharmaceutical ingredients (APIs). It is often employed in peptide synthesis and the creation of biologically active compounds, where precise stereochemical control is essential. Additionally, it is utilized in organic chemistry to facilitate the formation of specific chiral centers, enhancing the efficiency and selectivity of synthetic routes. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, making it a reliable reagent in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,196.00 |
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(R)-3-(tert-Butoxycarbonyl)-2,2-dimethyloxazolidine-4-carboxylic acid
This chemical is primarily used as a chiral auxiliary or building block in asymmetric synthesis. It plays a crucial role in the preparation of enantiomerically pure compounds, particularly in pharmaceutical research and development. Its structure is valuable for controlling stereochemistry during the synthesis of complex molecules, such as active pharmaceutical ingredients (APIs). It is often employed in peptide synthesis and the creation of biologically active compounds, where precise stereochemical control is essential. Additionally, it is utilized in organic chemistry to facilitate the formation of specific chiral centers, enhancing the efficiency and selectivity of synthetic routes. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, making it a reliable reagent in multi-step synthetic processes.
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