7-Boc-1,7-Diaza-spiro[4.4]nonane
95%
- Product Code: 74902
CAS:
646055-63-2
| Molecular Weight: | 226.32 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD09266216 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring a Boc-protected amine and a spirocyclic framework, makes it valuable in the design and synthesis of pharmaceuticals, especially those targeting neurological disorders. The Boc group provides a protective layer that can be easily removed under mild conditions, allowing for further functionalization of the molecule. Additionally, its spirocyclic nature contributes to the rigidity and stability of the compounds it forms, which is advantageous in drug discovery for enhancing binding affinity and selectivity towards biological targets. It is also explored in the creation of novel ligands for receptors and enzymes, contributing to advancements in medicinal chemistry and drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿7,980.00 |
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| 0.250 | 10-20 days | ฿36,800.00 |
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7-Boc-1,7-Diaza-spiro[4.4]nonane
This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring a Boc-protected amine and a spirocyclic framework, makes it valuable in the design and synthesis of pharmaceuticals, especially those targeting neurological disorders. The Boc group provides a protective layer that can be easily removed under mild conditions, allowing for further functionalization of the molecule. Additionally, its spirocyclic nature contributes to the rigidity and stability of the compounds it forms, which is advantageous in drug discovery for enhancing binding affinity and selectivity towards biological targets. It is also explored in the creation of novel ligands for receptors and enzymes, contributing to advancements in medicinal chemistry and drug development.
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