TERT-BUTYL 4-OXO-6-AZASPIRO[2.5]OCTANE-6-CARBOXYLATE
97%
- Product Code: 75909
CAS:
1101840-74-7
| Molecular Weight: | 225.38 g./mol | Molecular Formula: | C₁₂H₁₉NO₃ |
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| EC Number: | MDL Number: | MFCD21607170 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
TERT-BUTYL 4-OXO-6-AZASPIRO[2.5]OCTANE-6-CARBOXYLATE is primarily used in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its spirocyclic structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of molecules with potential biological activity. It is often employed in medicinal chemistry research for the design and optimization of drug candidates, especially those targeting neurological or metabolic disorders. The compound’s reactivity allows for modifications at specific sites, enabling the production of derivatives with tailored properties. Additionally, it is utilized in academic and industrial laboratories for studying reaction mechanisms and developing novel synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿112,040.00 |
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| 5.000 | 10-20 days | ฿335,890.00 |
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TERT-BUTYL 4-OXO-6-AZASPIRO[2.5]OCTANE-6-CARBOXYLATE
TERT-BUTYL 4-OXO-6-AZASPIRO[2.5]OCTANE-6-CARBOXYLATE is primarily used in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its spirocyclic structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of molecules with potential biological activity. It is often employed in medicinal chemistry research for the design and optimization of drug candidates, especially those targeting neurological or metabolic disorders. The compound’s reactivity allows for modifications at specific sites, enabling the production of derivatives with tailored properties. Additionally, it is utilized in academic and industrial laboratories for studying reaction mechanisms and developing novel synthetic pathways.
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