2-Azaspiro[3.3]heptane-2-carboxylic acid tert-butyl ester
95%
- Product Code: 75289
CAS:
1259489-92-3
| Molecular Weight: | 197.28 g./mol | Molecular Formula: | C₁₁H₁₉NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18325169 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This compound is primarily utilized in organic synthesis as a building block or intermediate for the development of more complex molecules. Its spirocyclic structure makes it valuable in medicinal chemistry, particularly in the design of drug candidates targeting neurological disorders. The tert-butyl ester group enhances its stability and solubility, facilitating its use in various chemical reactions. It is also employed in the synthesis of peptide mimetics and other bioactive compounds, where its unique structure can impart specific conformational properties to the final product. Additionally, it serves as a precursor in the preparation of heterocyclic compounds, which are often explored for their potential pharmacological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿37,035.00 |
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| 0.250 | 10-20 days | ฿61,128.00 |
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2-Azaspiro[3.3]heptane-2-carboxylic acid tert-butyl ester
This compound is primarily utilized in organic synthesis as a building block or intermediate for the development of more complex molecules. Its spirocyclic structure makes it valuable in medicinal chemistry, particularly in the design of drug candidates targeting neurological disorders. The tert-butyl ester group enhances its stability and solubility, facilitating its use in various chemical reactions. It is also employed in the synthesis of peptide mimetics and other bioactive compounds, where its unique structure can impart specific conformational properties to the final product. Additionally, it serves as a precursor in the preparation of heterocyclic compounds, which are often explored for their potential pharmacological activities.
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