1-Piperidinecarboxylic acid, 4-(aminomethyl)-3-hydroxy-,1,1-dimethylethyl ester, (3S,4S)-
97%
- Product Code: 222644
CAS:
279247-20-0
Molecular Weight: | 230.308 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₃ |
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Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of protease inhibitors, particularly in the development of antiviral drugs. Its stereochemistry and functional groups enable selective reactions that are crucial for building complex drug molecules. It is especially valuable in the synthesis of HIV and HCV therapeutics, where precise 3D orientation enhances drug efficacy and reduces side effects. The tert-butyl carbamate (Boc) protection group allows for controlled deprotection during multi-step syntheses, making it ideal for peptide and peptidomimetic applications. Its hydroxy and aminomethyl functionalities provide sites for further chemical modification, supporting the creation of diverse bioactive structures.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.100 | 10-20 days | $411.43 |
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1-Piperidinecarboxylic acid, 4-(aminomethyl)-3-hydroxy-,1,1-dimethylethyl ester, (3S,4S)-
Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of protease inhibitors, particularly in the development of antiviral drugs. Its stereochemistry and functional groups enable selective reactions that are crucial for building complex drug molecules. It is especially valuable in the synthesis of HIV and HCV therapeutics, where precise 3D orientation enhances drug efficacy and reduces side effects. The tert-butyl carbamate (Boc) protection group allows for controlled deprotection during multi-step syntheses, making it ideal for peptide and peptidomimetic applications. Its hydroxy and aminomethyl functionalities provide sites for further chemical modification, supporting the creation of diverse bioactive structures.
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