8-(tert-Butoxycarbonyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxylic acid
95%
- Product Code: 67954
CAS:
479636-66-3
| Molecular Weight: | 284 g./mol | Molecular Formula: | C₁₃H₂₀N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12198539 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed and dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the preparation of spirocyclic compounds, which are of significant interest in medicinal chemistry due to their structural complexity and potential biological activity. The tert-butoxycarbonyl (Boc) protecting group in the molecule is particularly valuable, as it can be easily removed under mild acidic conditions, allowing for further functionalization. This compound is often employed in the synthesis of peptidomimetics and other bioactive molecules, where the spirocyclic structure can enhance stability and selectivity. Additionally, its carboxylic acid group provides a handle for further chemical modifications, making it a versatile reagent in drug discovery and pharmaceutical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿88,960.00 |
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| 5.000 | 10-20 days | ฿280,470.00 |
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8-(tert-Butoxycarbonyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxylic acid
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the preparation of spirocyclic compounds, which are of significant interest in medicinal chemistry due to their structural complexity and potential biological activity. The tert-butoxycarbonyl (Boc) protecting group in the molecule is particularly valuable, as it can be easily removed under mild acidic conditions, allowing for further functionalization. This compound is often employed in the synthesis of peptidomimetics and other bioactive molecules, where the spirocyclic structure can enhance stability and selectivity. Additionally, its carboxylic acid group provides a handle for further chemical modifications, making it a versatile reagent in drug discovery and pharmaceutical research.
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