(S)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid
97%
- Product Code: 113809
CAS:
783349-78-0
| Molecular Weight: | 259.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₅ |
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| EC Number: | MDL Number: | MFCD11053524 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a morpholine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it a valuable intermediate in organic synthesis. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in ensuring the desired pharmacological activity. Additionally, it is used in peptide synthesis, where the Boc group protects amine functionalities during the coupling process. Its application extends to medicinal chemistry research, where it aids in the creation of novel drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,056.00 |
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| 0.250 | 10-20 days | ฿11,520.00 |
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| 1.000 | 10-20 days | ฿28,881.00 |
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(S)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a morpholine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it a valuable intermediate in organic synthesis. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in ensuring the desired pharmacological activity. Additionally, it is used in peptide synthesis, where the Boc group protects amine functionalities during the coupling process. Its application extends to medicinal chemistry research, where it aids in the creation of novel drug candidates with improved efficacy and selectivity.
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