tert-Butyl 1-cyano-6-azaspiro[2.5]octane-6-carboxylate
95%
- Product Code: 75987
CAS:
1174006-82-6
| Molecular Weight: | 236 g./mol | Molecular Formula: | C₁₃H₂₀N₂O₂ |
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| EC Number: | MDL Number: | MFCD12546363 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its unique spirocyclic structure makes it a valuable intermediate for constructing complex molecules, especially those targeting neurological and central nervous system disorders. Researchers often employ it in the synthesis of potential drug candidates due to its ability to introduce both cyano and carboxylate functional groups, which are crucial for enhancing binding affinity and metabolic stability. Additionally, it serves as a building block in the preparation of spirocyclic scaffolds, which are increasingly important in medicinal chemistry for their diverse biological activities. Its application extends to the study of enzyme inhibitors and receptor modulators, contributing to advancements in drug discovery and therapeutic development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿126,560.00 |
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| 1.000 | 10-20 days | ฿316,050.00 |
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tert-Butyl 1-cyano-6-azaspiro[2.5]octane-6-carboxylate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its unique spirocyclic structure makes it a valuable intermediate for constructing complex molecules, especially those targeting neurological and central nervous system disorders. Researchers often employ it in the synthesis of potential drug candidates due to its ability to introduce both cyano and carboxylate functional groups, which are crucial for enhancing binding affinity and metabolic stability. Additionally, it serves as a building block in the preparation of spirocyclic scaffolds, which are increasingly important in medicinal chemistry for their diverse biological activities. Its application extends to the study of enzyme inhibitors and receptor modulators, contributing to advancements in drug discovery and therapeutic development.
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