6-Hydroxy-2-azaspiro[3.3]heptane-2-carboxylic acid tert-butyl ester
98%
- Product Code: 75731
CAS:
1147557-97-8
| Molecular Weight: | 213.28 g./mol | Molecular Formula: | C₁₁H₁₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15071431 | |
| Melting Point: | 127-129℃ | Boiling Point: | |
| Density: | 1.17g/ml | Storage Condition: | 2-8℃, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its unique spirocyclic structure makes it valuable for designing and producing novel drug candidates, especially in the field of medicinal chemistry. Researchers often employ it to create compounds targeting neurological disorders, as its structural features can interact with specific biological receptors. Additionally, it serves as a building block in organic synthesis, enabling the creation of diverse chemical entities with potential therapeutic applications. Its tert-butyl ester group provides stability during synthetic processes, making it a practical choice for multi-step reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿387.00 |
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| 0.250 | 10-20 days | ฿648.00 |
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| 1.000 | 10-20 days | ฿2,007.00 |
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| 5.000 | 10-20 days | ฿6,705.00 |
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6-Hydroxy-2-azaspiro[3.3]heptane-2-carboxylic acid tert-butyl ester
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its unique spirocyclic structure makes it valuable for designing and producing novel drug candidates, especially in the field of medicinal chemistry. Researchers often employ it to create compounds targeting neurological disorders, as its structural features can interact with specific biological receptors. Additionally, it serves as a building block in organic synthesis, enabling the creation of diverse chemical entities with potential therapeutic applications. Its tert-butyl ester group provides stability during synthetic processes, making it a practical choice for multi-step reactions.
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