(1S,3S,4S,5R)-Rel-2-Boc-5-hydroxy-2-azabicyclo-[2.2.1]heptane-3-carboxylic acid
95%
- Product Code: 87925
CAS:
1290625-54-5
| Molecular Weight: | 257.28 g./mol | Molecular Formula: | C₁₂H₁₉NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24843160 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily used in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals. Its unique bicyclic structure makes it a valuable intermediate in the preparation of chiral compounds, which are essential in creating drugs with specific biological activities. It is often employed in the production of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. Additionally, its Boc-protected amine group allows for selective reactions, making it a versatile building block in medicinal chemistry. The compound’s stereochemistry also plays a significant role in enhancing the efficacy and specificity of the final drug molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿25,875.00 |
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(1S,3S,4S,5R)-Rel-2-Boc-5-hydroxy-2-azabicyclo-[2.2.1]heptane-3-carboxylic acid
This compound is primarily used in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals. Its unique bicyclic structure makes it a valuable intermediate in the preparation of chiral compounds, which are essential in creating drugs with specific biological activities. It is often employed in the production of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. Additionally, its Boc-protected amine group allows for selective reactions, making it a versatile building block in medicinal chemistry. The compound’s stereochemistry also plays a significant role in enhancing the efficacy and specificity of the final drug molecules.
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