(S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate
98%
- Product Code: 37131
CAS:
144282-37-1
| Molecular Weight: | 302.42 g./mol | Molecular Formula: | C₁₈H₂₆N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17214772 | |
| Melting Point: | Boiling Point: | 420.48°C | |
| Density: | 1.129g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic ring system, is particularly valuable in the development of pharmaceutical agents targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects on neurological disorders, such as anxiety, depression, and neurodegenerative diseases. Additionally, its tert-butyl carbamate group serves as a protective moiety during synthetic processes, enabling selective reactions and enhancing the stability of the intermediate. Its application extends to drug discovery programs where it aids in the optimization of pharmacokinetic properties and biological activity of lead compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,520.00 |
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| 1.000 | 10-20 days | ฿4,860.00 |
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(S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic ring system, is particularly valuable in the development of pharmaceutical agents targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects on neurological disorders, such as anxiety, depression, and neurodegenerative diseases. Additionally, its tert-butyl carbamate group serves as a protective moiety during synthetic processes, enabling selective reactions and enhancing the stability of the intermediate. Its application extends to drug discovery programs where it aids in the optimization of pharmacokinetic properties and biological activity of lead compounds.
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