N-tert-butoxycarbonyl-8-azabicyclo [3.2.1] octane-3-carboxylic acid
95%
- Product Code: 51656
CAS:
1159826-74-0
| Molecular Weight: | 255.31 g./mol | Molecular Formula: | C₁₃H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12068415 | |
| Melting Point: | Boiling Point: | 386.0±35.0 °C at 760 mmHg | |
| Density: | 1.196±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, including potential drugs targeting the central nervous system. Its bicyclic structure makes it valuable for creating rigid frameworks that can enhance the binding affinity of drug candidates to specific biological targets. Additionally, it is often employed in peptide synthesis, where the N-tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during multi-step processes. Its application extends to the production of chiral compounds, where its stereochemistry is leveraged to achieve high enantiomeric purity in final products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $137.68 |
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| 1.000 | 10-20 days | $340.48 |
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| 5.000 | 10-20 days | $1,180.72 |
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N-tert-butoxycarbonyl-8-azabicyclo [3.2.1] octane-3-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, including potential drugs targeting the central nervous system. Its bicyclic structure makes it valuable for creating rigid frameworks that can enhance the binding affinity of drug candidates to specific biological targets. Additionally, it is often employed in peptide synthesis, where the N-tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during multi-step processes. Its application extends to the production of chiral compounds, where its stereochemistry is leveraged to achieve high enantiomeric purity in final products.
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