2,6-Diaza-spiro[3.5]nonane-6-carboxylic acid tert-butyl ester hydrochloride
98%
- Product Code: 75097
CAS:
885272-17-3
| Molecular Weight: | 262.78 g./mol | Molecular Formula: | C₁₂H₂₃ClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22380770 | |
| Melting Point: | Boiling Point: | 319.4℃ at 760 mmHg | |
| Density: | 1.08g/ml | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily used in organic synthesis as a building block or intermediate for the development of more complex molecules. Its spirocyclic structure makes it valuable in medicinal chemistry, particularly in the design of drug candidates targeting various biological pathways. The tert-butyl ester group provides stability and facilitates further chemical modifications, while the hydrochloride salt form enhances its solubility and handling properties. It is often employed in the synthesis of peptidomimetics and other bioactive compounds, contributing to research in drug discovery and development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to light yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,480.00 |
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| 0.250 | 10-20 days | ฿13,880.00 |
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2,6-Diaza-spiro[3.5]nonane-6-carboxylic acid tert-butyl ester hydrochloride
This compound is primarily used in organic synthesis as a building block or intermediate for the development of more complex molecules. Its spirocyclic structure makes it valuable in medicinal chemistry, particularly in the design of drug candidates targeting various biological pathways. The tert-butyl ester group provides stability and facilitates further chemical modifications, while the hydrochloride salt form enhances its solubility and handling properties. It is often employed in the synthesis of peptidomimetics and other bioactive compounds, contributing to research in drug discovery and development.
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