1'-(tert-Butoxycarbonyl)-spiro[bicyclo[2.2.1]-hept[2]ene-7,4'-piperidine]-5-carboxylic acid
95%
- Product Code: 74815
CAS:
1251015-75-4
| Molecular Weight: | 307.39 g./mol | Molecular Formula: | C₁₇H₂₅NO₄ |
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| EC Number: | MDL Number: | MFCD12198776 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of biologically active compounds. Its structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing rigid frameworks and protecting amine functionalities during multi-step reactions. It is often employed in the preparation of drug candidates targeting neurological disorders, as the spirocyclic and piperidine motifs are common in central nervous system (CNS) active agents. Additionally, its carboxylic acid group allows for further functionalization, enabling its use in the creation of diverse chemical libraries for drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.001 | 10-20 days | $154.46 |
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| 0.002 | 10-20 days | $231.95 |
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1'-(tert-Butoxycarbonyl)-spiro[bicyclo[2.2.1]-hept[2]ene-7,4'-piperidine]-5-carboxylic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of biologically active compounds. Its structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing rigid frameworks and protecting amine functionalities during multi-step reactions. It is often employed in the preparation of drug candidates targeting neurological disorders, as the spirocyclic and piperidine motifs are common in central nervous system (CNS) active agents. Additionally, its carboxylic acid group allows for further functionalization, enabling its use in the creation of diverse chemical libraries for drug discovery.
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