(R)-methyl 3-bromo-2-((tert-butoxycarbonyl)amino)propanoate
98%
- Product Code: 232220
CAS:
175844-11-8
| Molecular Weight: | 282.13 g./mol | Molecular Formula: | C₉H₁₆BrNO₄ |
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| EC Number: | MDL Number: | MFCD09261317 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the preparation of β-amino acids and peptidomimetic compounds. Its protected amine and activated ester functionalities allow selective coupling reactions in multi-step organic syntheses. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. The bromine atom serves as a leaving group, enabling further functionalization via nucleophilic substitution or cross-coupling reactions. Widely utilized in medicinal chemistry for structure-activity relationship studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $214.57 |
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| 5g | 10-20 days | $1,862.43 |
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| 1g | 10-20 days | $578.56 |
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(R)-methyl 3-bromo-2-((tert-butoxycarbonyl)amino)propanoate
Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the preparation of β-amino acids and peptidomimetic compounds. Its protected amine and activated ester functionalities allow selective coupling reactions in multi-step organic syntheses. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. The bromine atom serves as a leaving group, enabling further functionalization via nucleophilic substitution or cross-coupling reactions. Widely utilized in medicinal chemistry for structure-activity relationship studies.
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