tert-Butyl 2-azaspiro[3.3]heptan-6-ylcarbamate hemioxalate
95%
- Product Code: 76038
CAS:
1400764-62-6
| Molecular Weight: | 320.32 g./mol | Molecular Formula: | C₁₃H₂₂N₂O₆ |
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| EC Number: | MDL Number: | MFCD22421679 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a spirocyclic system, makes it a valuable building block for developing compounds with potential therapeutic applications. It is often employed in the design and production of drugs targeting neurological disorders, including those affecting the central nervous system. Additionally, its carbamate group enhances its stability and bioavailability, making it suitable for further chemical modifications. Researchers also explore its use in creating novel ligands for receptors involved in pain management and mental health conditions. Its hemioxalate form aids in improving solubility and handling during laboratory processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿63,900.00 |
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| 1.000 | 10-20 days | ฿175,930.00 |
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tert-Butyl 2-azaspiro[3.3]heptan-6-ylcarbamate hemioxalate
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a spirocyclic system, makes it a valuable building block for developing compounds with potential therapeutic applications. It is often employed in the design and production of drugs targeting neurological disorders, including those affecting the central nervous system. Additionally, its carbamate group enhances its stability and bioavailability, making it suitable for further chemical modifications. Researchers also explore its use in creating novel ligands for receptors involved in pain management and mental health conditions. Its hemioxalate form aids in improving solubility and handling during laboratory processes.
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