9-(tert-Butoxycarbonyl)-4-methyl-1-oxa-4,9-diazaspiro[5.5]undecane-2-carboxylic acid
95%
- Product Code: 121036
CAS:
1824018-10-1
| Molecular Weight: | 314.38 g./mol | Molecular Formula: | C₁₅H₂₆N₂O₅ |
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| EC Number: | MDL Number: | MFCD28119001 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of complex pharmaceutical compounds. Its unique structure, featuring a spirocyclic ring system and a protected amine group, makes it valuable for constructing molecules with specific biological activities. It is often employed in the synthesis of drugs targeting neurological disorders, as the spirocyclic framework can mimic certain natural substrates or receptors in the brain. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization of the molecule during multi-step synthetic processes. Its application is also seen in the development of peptidomimetics, where it serves as a building block to mimic peptide structures, enhancing stability and bioavailability of potential drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿23,850.00 |
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9-(tert-Butoxycarbonyl)-4-methyl-1-oxa-4,9-diazaspiro[5.5]undecane-2-carboxylic acid
This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of complex pharmaceutical compounds. Its unique structure, featuring a spirocyclic ring system and a protected amine group, makes it valuable for constructing molecules with specific biological activities. It is often employed in the synthesis of drugs targeting neurological disorders, as the spirocyclic framework can mimic certain natural substrates or receptors in the brain. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization of the molecule during multi-step synthetic processes. Its application is also seen in the development of peptidomimetics, where it serves as a building block to mimic peptide structures, enhancing stability and bioavailability of potential drug candidates.
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