tert-Butyl ((4-oxocyclohexyl)methyl)carbamate
96%
- Product Code: 149801
CAS:
809273-70-9
| Molecular Weight: | 227.3 g./mol | Molecular Formula: | C₁₂H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03839885 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure contains both a protected amine (via Boc group) and a ketone functionality, making it valuable in multi-step syntheses where selective reactions are required. Commonly employed in the development of bioactive compounds, including drug candidates targeting central nervous system disorders and anti-inflammatory agents. The ketone group allows for further derivatization, such as reduction or nucleophilic addition, while the Boc group ensures amine compatibility during reactions. Also utilized in the preparation of cyclic amines and constrained peptidomimetics due to its rigid cyclohexyl backbone.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $36.04 |
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| 1g | 10-20 days | $91.15 |
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| 5g | 10-20 days | $449.39 |
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| 25g | 10-20 days | $1,815.04 |
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tert-Butyl ((4-oxocyclohexyl)methyl)carbamate
Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure contains both a protected amine (via Boc group) and a ketone functionality, making it valuable in multi-step syntheses where selective reactions are required. Commonly employed in the development of bioactive compounds, including drug candidates targeting central nervous system disorders and anti-inflammatory agents. The ketone group allows for further derivatization, such as reduction or nucleophilic addition, while the Boc group ensures amine compatibility during reactions. Also utilized in the preparation of cyclic amines and constrained peptidomimetics due to its rigid cyclohexyl backbone.
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