(2R,4S)-3-(tert-Butoxycarbonyl)-2-(tert-butyl)-4-methyloxazolidine-4-carboxylic acid
98%
- Product Code: 123611
CAS:
1179522-58-7
| Molecular Weight: | 287.35 g./mol | Molecular Formula: | C₁₄H₂₅NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18837750 | |
| Melting Point: | 117-118 °C | Boiling Point: | 387.4±42.0 °C(Predicted) |
| Density: | 1.127±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral auxiliary or building block for the preparation of complex molecules, particularly in pharmaceutical research. Its structure is advantageous for stereocontrol in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. It is often employed in the synthesis of peptides, peptidomimetics, and other bioactive molecules where precise stereochemistry is critical. Additionally, its tert-butoxycarbonyl (Boc) protecting group is valuable in multi-step synthetic processes, as it can be easily removed under mild acidic conditions without affecting other functional groups. This makes it a versatile tool in the development of drugs and fine chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,378.00 |
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| 0.250 | 10-20 days | ฿15,930.00 |
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| 1.000 | 10-20 days | ฿43,002.00 |
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(2R,4S)-3-(tert-Butoxycarbonyl)-2-(tert-butyl)-4-methyloxazolidine-4-carboxylic acid
This compound is primarily utilized in organic synthesis as a chiral auxiliary or building block for the preparation of complex molecules, particularly in pharmaceutical research. Its structure is advantageous for stereocontrol in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. It is often employed in the synthesis of peptides, peptidomimetics, and other bioactive molecules where precise stereochemistry is critical. Additionally, its tert-butoxycarbonyl (Boc) protecting group is valuable in multi-step synthetic processes, as it can be easily removed under mild acidic conditions without affecting other functional groups. This makes it a versatile tool in the development of drugs and fine chemicals.
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