N-(2-Aminospiro[3.3]hept-6-yl)carbamic acid tert-butyl ester
95%
- Product Code: 75859
CAS:
1239589-52-6
| Molecular Weight: | 226.32 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09054707 | |
| Melting Point: | Boiling Point: | 345.1±41.0℃ at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its unique spirocyclic structure makes it valuable for creating novel drug candidates, particularly in the field of central nervous system (CNS) disorders. Researchers leverage its structural features to design compounds that target specific receptors or enzymes involved in neurological pathways. Additionally, it serves as a building block in medicinal chemistry for the development of potential therapeutics aimed at addressing conditions such as anxiety, depression, or neurodegenerative diseases. Its tert-butyl ester group provides stability during synthetic processes, enabling efficient modification and optimization of drug-like properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿10,560.00 |
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N-(2-Aminospiro[3.3]hept-6-yl)carbamic acid tert-butyl ester
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its unique spirocyclic structure makes it valuable for creating novel drug candidates, particularly in the field of central nervous system (CNS) disorders. Researchers leverage its structural features to design compounds that target specific receptors or enzymes involved in neurological pathways. Additionally, it serves as a building block in medicinal chemistry for the development of potential therapeutics aimed at addressing conditions such as anxiety, depression, or neurodegenerative diseases. Its tert-butyl ester group provides stability during synthetic processes, enabling efficient modification and optimization of drug-like properties.
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