N-Boc-7-Bromo-4-oxo-3,4-dihydro-1'H-spiro[chromene-2,4'-piperidine]
95%
- Product Code: 75855
CAS:
936648-38-3
| Molecular Weight: | 369.28 g./mol | Molecular Formula: | C₁₈H₂₂BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09991613 | |
| Melting Point: | Boiling Point: | 501.3℃ at 760 mmHg | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a Boc-protected amine and a bromo-substituted chromene, makes it valuable in medicinal chemistry for the creation of potential drug candidates. The Boc group allows for selective deprotection, enabling further functionalization, while the bromine atom serves as a reactive site for cross-coupling reactions, such as Suzuki or Heck reactions. This makes it particularly useful in the synthesis of biologically active compounds, including those targeting neurological or oncological pathways. Additionally, its spirocyclic framework is often explored in the design of novel therapeutic agents due to its potential to enhance molecular stability and binding affinity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿88,200.00 |
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| 5.000 | 10-20 days | ฿342,670.00 |
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N-Boc-7-Bromo-4-oxo-3,4-dihydro-1'H-spiro[chromene-2,4'-piperidine]
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a Boc-protected amine and a bromo-substituted chromene, makes it valuable in medicinal chemistry for the creation of potential drug candidates. The Boc group allows for selective deprotection, enabling further functionalization, while the bromine atom serves as a reactive site for cross-coupling reactions, such as Suzuki or Heck reactions. This makes it particularly useful in the synthesis of biologically active compounds, including those targeting neurological or oncological pathways. Additionally, its spirocyclic framework is often explored in the design of novel therapeutic agents due to its potential to enhance molecular stability and binding affinity.
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