5-(tert-Butoxycarbonyl)-5-azaspiro[2.4]heptane-7-carboxylic acid
96%
- Product Code: 124352
CAS:
1268519-54-5
| Molecular Weight: | 241.28 g./mol | Molecular Formula: | C₁₂H₁₉NO₄ |
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| EC Number: | MDL Number: | MFCD18633038 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a spirocyclic framework and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing nitrogen-containing heterocycles, which are common in drug discovery. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization of the molecule. It is often employed in the development of bioactive compounds, including potential therapeutic agents targeting neurological disorders or other diseases. Additionally, its spirocyclic nature contributes to the exploration of novel chemical space, aiding in the design of molecules with unique properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,672.00 |
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| 0.250 | 10-20 days | ฿19,008.00 |
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5-(tert-Butoxycarbonyl)-5-azaspiro[2.4]heptane-7-carboxylic acid
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a spirocyclic framework and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing nitrogen-containing heterocycles, which are common in drug discovery. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization of the molecule. It is often employed in the development of bioactive compounds, including potential therapeutic agents targeting neurological disorders or other diseases. Additionally, its spirocyclic nature contributes to the exploration of novel chemical space, aiding in the design of molecules with unique properties.
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