Tert-butyl trans-4-formylcyclohexylcarbamate
97%
- Product Code: 87879
CAS:
181308-57-6
| Molecular Weight: | 227.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₃ |
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| EC Number: | MDL Number: | MFCD03844598 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃, inert gas storage |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals and organic intermediates. Its structure, featuring both a formyl group and a carbamate moiety, makes it a versatile building block in medicinal chemistry. It is often employed in the development of drug candidates, particularly in the creation of protease inhibitors and other bioactive molecules. The tert-butyl group provides steric protection, enhancing the stability of intermediates during complex synthetic processes. Additionally, it is used in the preparation of chiral compounds, where the cyclohexyl ring can serve as a scaffold for asymmetric synthesis. Its applications extend to research in neurodegenerative diseases and cancer therapy, where it contributes to the design of targeted therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft12,605.71 |
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| 0.250 | 10-20 days | Ft18,520.69 |
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| 1.000 | 10-20 days | Ft47,610.78 |
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Tert-butyl trans-4-formylcyclohexylcarbamate
This compound is primarily utilized in the synthesis of pharmaceuticals and organic intermediates. Its structure, featuring both a formyl group and a carbamate moiety, makes it a versatile building block in medicinal chemistry. It is often employed in the development of drug candidates, particularly in the creation of protease inhibitors and other bioactive molecules. The tert-butyl group provides steric protection, enhancing the stability of intermediates during complex synthetic processes. Additionally, it is used in the preparation of chiral compounds, where the cyclohexyl ring can serve as a scaffold for asymmetric synthesis. Its applications extend to research in neurodegenerative diseases and cancer therapy, where it contributes to the design of targeted therapeutic agents.
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