tert-Butyl 2,5-diazabicyclo[4.1.0]heptane-2-carboxylate
98%
- Product Code: 150851
CAS:
1228675-18-0
| Molecular Weight: | 198.26 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17480504 | |
| Melting Point: | Boiling Point: | 276.4±15.0 °C(Predicted) | |
| Density: | 1.104±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals. Its strained bicyclic structure and protected amine functionalities make it valuable for constructing complex nitrogen-containing molecules. Commonly employed in the development of protease inhibitors and kinase inhibitors due to its ability to mimic peptide bonds and influence stereochemistry in drug candidates. Also utilized in agrochemicals for designing novel active ingredients with improved metabolic stability. The tert-butyl carbamate (Boc) group allows for selective deprotection, enabling stepwise assembly in multi-step organic syntheses.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Yellow Viscous Liquid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | €64.56 |
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| 250mg | 10-20 days | €126.23 |
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| 1g | 10-20 days | €352.87 |
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| 5g | 10-20 days | €1,482.09 |
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tert-Butyl 2,5-diazabicyclo[4.1.0]heptane-2-carboxylate
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals. Its strained bicyclic structure and protected amine functionalities make it valuable for constructing complex nitrogen-containing molecules. Commonly employed in the development of protease inhibitors and kinase inhibitors due to its ability to mimic peptide bonds and influence stereochemistry in drug candidates. Also utilized in agrochemicals for designing novel active ingredients with improved metabolic stability. The tert-butyl carbamate (Boc) group allows for selective deprotection, enabling stepwise assembly in multi-step organic syntheses.
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